Marina Machado
Cláudia R. Serra
Aires Oliva-Teles
Benjamín Costas- 1Centro Interdisciplinar de Investigação Marinha e Ambiental (CIIMAR), Matosinhos, Portugal
- 2Instituto de Investigação e Inovação em Saúde (i3S), Universidade do Porto, Porto, Portugal
- 3Instituto de Ciências Biomédicas Abel Salazar (ICBAS-UP), Universidade do Porto, Porto, Portugal
- 4Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal
- 5Departamento de Biologia, Faculdade de Ciências da Universidade do Porto (FCUP), Porto, Portugal
The range of metabolic pathways that are dependent on a proper supply of specific amino acids (AA) unveils their importance in the support of health. AA play central roles in key pathways vital for immune support and individual AA supplementation has shown to be able to modulate fish immunity. In vitro trials are important tools to evaluate the immunomodulatory role of AA, and the present study was conceived to evaluate methionine and tryptophan roles in immune-related mechanisms aiming to understand their effects in leucocyte functioning and AA pathways. For that purpose, head-kidney leucocytes were isolated and a primary cell culture established. The effect of methionine or tryptophan surplus on cell viability was assessed. Medium L-15 10% FBS without AA addition (0.5mM of L-methionine, 0.1 mM of L-tryptophan) was used as control. To that, L-methionine or L-tryptophan were supplemented at 1 and 2 times (M1x or M2x, and T1x or T2x). Nitric oxide, ATP, total antioxidant capacity, and immune-related genes were evaluated in response to lipopolysaccharides extracted from Photobacterium damselae subsp. piscicida or UV-inactivated bacteria). Moreover, caspase 3 activity and apoptosis-related genes were evaluated in response to the apoptosis-inducing protein, AIP56. Distinct roles in leucocytes’ immune response were observed, with contrasting outcomes in the modulation of individual pathways. Methionine surplus improved cell viability, polyamine production, and methionine-related genes expression in response to an inflammatory agent. Also, methionine supplementation lowered signals of apoptosis by AIP56, presenting lower caspase 3 activity and higher il1β and nf-κb expression. Cells cultured in tryptophan supplemented medium presented signals of an attenuated inflammatory response, with decreased ATP and enhanced expression of anti-inflammatory and catabolism-related genes in macrophages. In response to AIP56, leucocytes cultured in a tryptophan-rich medium presented lower resilience to the toxin, higher caspase 3 activity and expression of caspase 8, and lower expression of several genes, including nf-κb and p65. This study showed the ability of methionine surplus to improve leucocytes’ response to an inflammatory agent and to lower signals of apoptosis by AIP56 induction, while tryptophan attenuated several cellular signals of the inflammatory response to UV-inactivated bacteria and lowered leucocyte resilience to AIP56.
Introduction
Amino acids (AA) are key players for the biosynthesis of vital molecules for immune support (1) and their use as nutraceutical supplements in mammals (2) and poultry (3, 4) is a current strategy. The role of individual AA in the innate immune response is associated with their role in key pathways essential for cellular function and as precursors of hormones and enzymes. Likewise, following the presuppose that the requirement of specific AA increases in response to inflammation and infection (5), their dietary supplementation may allow the modulation of particular immune-related pathways with the final goal of enhancing host immunity. Having this in mind, in vivo studies were developed to achieve nutritional strategies that modulate the fish immune response through the increase of AA availability (6–14), while few in vitro studies (15, 16) aiming to collect information at the cellular level were performed.
Previous studies in fish contributed with some insights on the key role of methionine in the fish immune system. Dietary methionine supplementation was able to increase European seabass (Dicentrarchus labrax) peripheral neutrophil numbers and innate immune response to an inflammatory insult with UV-inactivated Photobacterium damselae subsp. piscicida (Phdp) (11, 13) and increase disease resistance to Phdp (14). Also, juvenile Jian carp (Cyprinus carpio var. Jian) fed with increased levels of methionine presented an increased peripheral leucocyte concentration and humoral response, in response to Aeromonas hydrophila (9). Additionally, methionine supplementation was shown to be key for European seabass immune support in an extreme feed formulation (0% fish meal) (17). Data from those studies are sustained by the recognized role of methionine as a methyl group donor for the methylation, transsulfuration, and aminopropylation routes, with coenzyme S-adenosylmethionine (SAM) as the leading factor. The increase of methionine input can increase DNA methylation ratio, known to be dependent on the supply of SAM (18). Through the aminopropylation route, methionine contributes to polyamine synthesis thus contributing to cell proliferation (19). Finally, by the transsulfuration pathway, methionine is the precursor of cysteine, an AA constituent of the powerful antioxidant molecule glutathione (GSH) (1). In vitro results on this matter are scarce. Nonetheless, Azeredo et al. (16) showed the ability of methionine supplementation to boost European seabass head-kidney (HK) leucocytes (HKL) nitric oxide (NO), superoxide anion, and ATP production in the absence of stimulus, and improved HKL NO production in response to UV-inactivated Vibrio anguillarum. These authors discussed that methionine potential for immune improvement seems to be directly related to the enhancement of cell response by the enhancement of the methionine-related pathways.
Tryptophan has been the target of in vivo studies in several animal models focusing its function as a precursor of compounds involved in stress modulation, antioxidant properties, and immune tolerance (20–22). Studies in fish showed that increasing dietary tryptophan levels did not significantly modulate European seabass (11) and Persian sturgeon (Acipenser persicus) (23) basal innate immune- related mechanisms activity, while a clear effect of tryptophan surplus was observed upon inflammation induction. For instance, in European seabass Azeredo et al. (12) observed an inhibitory action of tryptophan on HK inflammatory transcripts while Machado et al. (24) reported a compromised immune response and disease resistance to Phdp. In macrophages, tryptophan catabolism occurs through the kynurenine-niacin pathway, mediated by indoleamine 2, 3-dioxygenase (IDO) (25). In response to inflammation, IDO is induced, exerting anti-microbial effects by tryptophan extracellular depletion (26, 27), setting an antioxidant system by the consumption of superoxide radicals, and its metabolites regulate T-cell function (28). In vitro results pointed to the impairment of pro-inflammatory signals offsetting the inflammatory response caused by tryptophan higher availability (16).
The inflammatory response and the overall innate immune system is sustained by phagocytes (i.e. neutrophils and macrophages). These myeloid cells are responsible for the incorporation and digestion of other cells or cell components, as pathogens or apoptotic and necrotic host-cells. Moreover, fish phagocytes are responsible for the initiation and resolution of inflammation by the production and secretion of pro- and anti-inflammatory chemical messengers (autocrine signaling) and cell-to-cell signaling communication (paracrine signaling) (29). In fact, as widely described in mammals, monocytes can adapt their phenotypes according to the response stage and differentiated into three distinct groups formerly determined by the inductor of differentiation (30–33). Upon activation, circulating monocytes (M0 type) are differentiated into macrophages that under inflammatory settings and in the presence of pathogens and tumor cells, are described as M1 type. Whereas M2 macrophages are found in sterile conditions or in the repair stage of the innate response (34). This has only been recently described in fish, particularly in the common carp (Cyprinus carpio L) (35). Additionally, cell inactivation and clearance through apoptosis takes part in the proper function of the immune system. As a defense mechanism, apoptosis is responsible for the clearance of damaged cells and can be initiated by a wide variety of stimuli, as infection and stress (36). Since macrophages present themselves as a useful tool for in vitro functional studies on the fish innate immune response, the present work focused on the study of the response of innate activated macrophages induced by microbial stimuli and with key roles in the phagocytosis of pathogens and the production of pro-inflammatory signals (37).
Phdp is a bacterial pathogen for many marine fish species that owns part its successful pathogenesis to the ability to produce and release the exotoxin AIP56 to the extracellular environment (38). AIP56 cleaves the transcription factor NF- κB, therefore inhibiting the transcription of key immune-related genes (39) and inducing extensive apoptosis of macrophages and neutrophils (38). Therefore, Phdp can act at distance, without direct contact with the host cells, and leads to the depletion of host primary cell defense mechanisms, the phagocytes.
The present study aimed to evaluate in vitro, at the leucocytes functional and transcriptional level, the modulatory effects of two supplementation levels of methionine and tryptophan on the response of HKL against UV- inactivated Phdp (PhdpUV) or Phdp lipopolysaccharides (LPSPhdp), and the apoptosis process in response to the AIP56 toxin.
Material and Methods
The experiments were approved by the CIIMAR Animal Welfare Committee, carried out in a registered installation (N16091.UDER), and performed by trained scientists in full compliance with national rules and following the European Directive 2010/63/EU of the European Parliament and the European Union Council on the protection of animals used for scientific purposes.
Photobacterium damselae subsp. piscicida Inactivation
Phdp strain PP3, isolated from yellowtail (Seriola quinqueradiata; Japan), was obtained from the Fish Immunology and Vaccinology group (i3S/IBMC, University of Porto). Bacteria were routinely cultured at 22°C in tryptic soy broth (TSB) or tryptic soy agar (TSA) (both from Difco Laboratories) supplemented with NaCl to a final concentration of 2% (w/v) (TSB-2 and TSA-2, respectively). Live bacteria were stored at −80°C in TSB-2 supplemented with 15% (v/v) glycerol.
To maintain the structural integrity of bacterial antigens but prevent bacterial growth, Phdp were killed by UV irradiation. For this, bacteria were grown in TSB-2 and, after reaching the exponential growth phase (OD600nm= 0.523; 6.7 x 108 colony forming units (CFUs) ml-1), were placed in a sterile tray (maximum inoculum height of 0.2 mm) at a distance of 10 centimeters of a UV lamp and inactivated by exposure to UV irradiation for 2 h. Bacteria were then recovered by centrifugation at 1500 × g for 30 min, the pellet resuspended in Hank’s Balanced Salt Solution (HBSS, Gibco), and bacterial concentration adjusted to a virtual dose of 1 × 107 CFU ml-1 taking into account their concentration prior to inactivation. Lack of bacterial viability was confirmed by plating the inoculum on TSA-2.
Photobacterium damselae subsp. piscicida Lipopolysaccharides Extraction and Purification
Lipopolysaccharides (LPS) from Phdp (LPSPhdp) were extracted by hot phenol-water according to the method described by Rezania et al. (40) with modifications (16). Purified LPSPhdp, without any residual phenol, was lyophilized, resuspended in PBS to a final concentration of 2 mg ml−1, and kept at −20°C until use. Visualization was achieved by SDS-PAGE (12%) electrophoretic resolution of 20 µg purified LPSPhdp and consequent staining following the improved silver stain protocol described by Zhu et al. (41).
Recombinant AIP56
Recombinant AIP56 (38) was obtained from the Fish Immunology and Vaccinology group (i3S/IBMC, University of Porto) and stored in 20 nM Tris-HCl, pH 8.0 at -80 °C until use.
Fish and Establishment of HKL Primary Cell Cultures
European seabass (Dicentrarchus labrax) juveniles (8 ± 0.5 g) were obtained from a certified hatchery (MARESA, Spain), acclimatized to laboratory conditions, and reared for 2 years in a recirculation water system to a final body weight of 700 ± 50 g. Water parameters were maintained as followed: O2 saturation at 7.38 ± 0.01 mg/l, salinity at 35 ppt, temperature at 18°C, and 10 h dark: 14 h light photoperiod. Fish were daily fed a commercial diet (Sorgal, Portugal) and no clinical signs of disease and illness were observed.
European seabass were euthanized by an overdose of anesthetic (>1ml/l, 2-phenoxyethanol, Merck) and bled by collecting blood from the caudal vessels using a heparinized vacuum system and cut off the branchial arches. HKL were isolated and maintained following Secombes (42) with modifications. The head-kidney was aseptically removed and the tissue disrupted by passing through a 100 µl nylon mesh in 30 mL of Leibovitz L-15 medium (L-15, Gibco) supplemented with 2% fetal bovine serum (FBS, Gibco), 100 IU ml-1 penicillin and streptomycin (Gibco), and 30 U ml-1 heparin (Braun) (L-15 2% FBS). After centrifugation, a clear separation between leucocytes and erythrocytes was observed and the upper leucocyte layer was carefully collected and separated from the erythrocytes bottom layer and the resulting cell suspension was resuspended in fresh L-15 2% FBS and centrifuged at 600 × g at 4°C for 10 minutes. The collected leucocytes were washed two times at 600 × g at 4°C for 10 minutes and finally resuspended in L-15 medium with 0.1% FBS (L-15 0.1% FBS) and antibiotics. Leucocytes viability was determined by the trypan blue exclusion method. Leucocytes were diluted four times in a 0.4% trypan blue solution and concentration adjusted to 1 × 107 viable cells ml-1 after counting in a hemocytometer. One hundred microliters of the leucocyte suspension were plated in 96-well plate for ATP, total antioxidants concentration (TAC), polyamines, nitric oxide (NO), and caspase 3-active assays. For gene expression, 500 µl of the leucocyte suspension was plated in 24-well plates.
Experimental Design
After primary cell culture isolation and plating, the leucocyte monolayer was maintained for 2 h in L-15 2% FBS for cell adhesion and subsequently washed with HBSS, removing non-adherent cells. Adherent cells, characterized mostly by the monocyte lineage (43) were then incubated with fresh L-15 10% FBS supplemented with methionine or tryptophan for 24 h at 18 °C and leucocyte viability was evaluated by the 3-(4,5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assay. Two supplementation levels of each AA were selected based in previous studies (16). Both AA were supplemented at 1 × or 2 × the basal concentration found in L-15 with the final concentration of L-methionine (M1x, 1mM or M2x, 1.5 mM) and L-tryptophan (T1x, 0.2 mM or T2x, 0.3 mM). As a control, L-15 10% FBS without AA addition was used (containing 0.5mM of L-methionine and 0.1 mM of L-tryptophan, Gibco).
Two trials, each comprising a total of six fish were performed (Figure 1). Cellular response (Trial 1) was assessed upon stimulation with PhdpUV (1 × 106 CFU ml-1 with an expected LPS concentration of 0.006 µg ml-1), LPSPhdp (10 µg ml-1), or the absence of a stimulus (Ø). Concentration of each stimulus was selected according to (16). Gene expression, ATP, and TAC were measured at the end of 4 and 24 h of stimulation since most innate immune mechanisms are activated upon acute stimulation. Polyamines production was evaluated in L-15, M1x, and M2x after 48 h of stimulation since methionine has a direct role in polyamine biosynthesis (19), but only in PhdpUV and Ø treatments due to technical limitations. Finally, NO production was evaluated at 72 and 96 h according to previous studies (16, 44). The apoptosis assays (Trial 2) consisted of evaluating caspase 3-active and gene expression in response to AIP56 protein (2 µg ml-1) (45) or in Ø during a time-course study (i.e. 1, 3, and 6 h) with the cell culture media replaced by a fresh solution at each hour. Staurosporine (2.33 µg ml-1, Sigma) was used in L-15 wells as a positive control for apoptosis (46).
Figure 1 Experimental design. L-15 (Leibowitz L-15 medium); M1x (Leibowitz L-15 medium supplemented with 1 mM of L-methionine); M2x (Leibowitz L-15 medium supplemented with 1.5 mM of L-methionine); T1x (Leibowitz L-15 medium supplemented 0.2 mM of L-tryptophan); T2x (Leibowitz L-15 medium supplemented 0.3 mM of L-tryptophan); MTT (3-(4,5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide assay); Ø (unstimulated cells); LPSPhdp (Lipopolysaccharides extracted from Phdp); PhdpUV (UV-inactivated Phdp); ATP (Adenosine triphosphate); TAC (total antioxidant capacity); NO (nitric oxide).
All analyses were performed with triplicate analytic replicates in a total of six biological replicates.
MTT Assay
The leucocytes viability was assessed by the MTT reduction by the NAD(P)H-dependent cellular oxidoreductase enzymes produced under cell metabolic activity, reflecting the number of viable cells (47). After 24 h incubation at 18 °C in L-15 10% FBS supplemented with the desired AA, 20 µl of MTT (5 mg ml-1) was added to each well and incubated for 4 h at 18 °C. After centrifugation at 110 × g for 5 min, the insoluble resultant formazan was dissolved in 100 µl of dimethyl sulfoxide (DMSO) and the absorbance read at 550 nm (Synergy HT, Biotek). A total of twelve biological replicates were evaluated (6 biological replicates per trial).
Immune Assays
ATP Assay
ATP production by the leucocytes monolayers incubated with LPSPhdp, PhdpUV, or in the absence of stimuli for 4 and 24 h with each AA treatment was measured with an ATP Colorimetric Assay Kit (Sigma). From each well, 50 µl of the cell supernatant was transferred to a new 96-well plate and the protocol performed according to the manufacture’s indications. The absorbance was read at 570 nm (Synergy HT, Biotek) and ATP concentration was calculated according to a standard ATP curve after subtraction of background absorbance values.
TAC Assay
The total antioxidants concentration (TAC), such us oxygen species and reactive nitrogen species, was determined in the supernatant of cells incubated with LPSPhdp, PhdpUV, or Ø during 4 and 24 h and previously incubated for 24 h with the different AA treatments. Cell supernatants were collected, diluted in Protein Mask in a 1:1 ratio according to manufacturer’s indications (The Total Antioxidant Capacity Kit, Sigma), and 100 µl of the mixture was added to a 96-well plate and the protocol performed. The absorbance was read at 570 nm (Synergy HT, Biotek). Background absorbance values were subtracted and TAC concentration was calculated from a standard curve.
Polyamines Assay
The Total Polyamine Assay Kit (BioVision) was used for fluorometric assessment of polyamine content in cells either stimulated with PhdpUV or unstimulated for 48 h after incubation with L-15, M1x, or M2x for 24 h. According to the manufacturer’s indications, a sample background wells fluorescence (Ex/Em= 535/587 nm) was subtracted to the standards and reaction wells and the concentration determined according to the standard curve previously prepared.
NO Assay
NO production was measured in the supernatant collected from leucocyte primary cell cultures formerly incubated with the different AA treatments for 24 h and stimulated with PhdpLPS, PhdpUV, or in the absence of stimuli for 72 or 96 h. At each time, 50 µl of supernatant was transferred to a new 96-well plate and total nitrite and nitrate concentrations in the sample were assessed using the Nitrite/Nitrate colorimetric method kit (Roche). Nitrite concentration was calculated by comparison with a sodium nitrite standard curve. Since nitrite and nitrate are endogenously produced as oxidative metabolites of the messenger molecule NO, these compounds are considered as indicative of NO production.
Apoptosis Assays
After incubation for 24 h with the different AA treatments, the cell culture media was replaced by a fresh solution without stimuli or containing AIP56. The medium was renewed at each hourly, for 6 h (45), and cells collected for caspase 3-active assay or for gene expression after 1, 3 and 6 hours. The inability of the AA, at the highest supplementation level, to inhibit AIP56 activity on the cleavage of the leucocytes p65 subunit was tested by SDS-PAGE and Western blotting.
SDS-PAGE and Western Blotting
Leucocytes from four fish were incubated with L-15, M2x or T2x during 24h and afterwards incubated the with Ø or 2 µg ml-1 of AIP56 for 2 h. Supernatant was removed and cells (5× 106 cells) were lysed and collected by adding 40 µl SDS-PAGE sample buffer (50mMTris-HCl [pH 8.8], 2% SDS, 0.05% bromophenol blue, 10% glycerol, 2mM EDTA, and 100 mM DTT) (48). Samples were then boiled for 5 min and 20 µl (2.5× 106 cells) were loaded For Western blotting, the proteins were transferred onto nitrocellulose membranes. The efficiency of transfer and the protein loading on the membranes was controlled by staining with Ponceau S. The membranes were blocked for 1 h at room temperature (RT) with 5% skim milk in Tris-buffered saline (TBS) containing 0.1% Tween 20 (T-TBS) followed by incubation for 1 h at RT with the anti-sea bass NF- κB p65 rabbit serum diluted in blocking buffer (1:500) (49). Immunoreactive bands were detected using alkaline phosphatase-conjugated secondary antibodies (1:0000) and nitrobluetetrazolium–5-bromo-4-chloro-3-indolylphosphate (NBT/BCIP) (Promega).
Caspase 3-Active
The caspase 3-active assay was performed for each AA treatment in cells stimulated for 1, 3, and 6 h with AIP56. Cells without stimuli were used as control. The assay kit (Abcam) quantifies the cleavage of a substrate by caspase 3 or related caspases. The fluorescence (Ex/Em= 400/505 nm) was read and the fold-increase in caspase 3 activity was determined by comparing with the level determined in unstimulated cells cultured with L-15.
Gene Expression
Total RNA was extracted from cells collected for innate immune response and apoptosis as following. After supernatant collection, wells were washed with HBSS and 50 µl of NZYol (NZYTech) reagent was added to each well, RNA was isolated following the manufacturer’s indications (NZY Total RNA Isolation kit) and resuspended in free nuclease water (NZYTech). RNA was quantified using the DS-11 Spectrophotometer (DeNovix) and samples were treated with DNase using RQ1 RNase-free DNase kit (Promega) following the manufacturer’s indications. First-strand cDNA was synthesized with NZY First-Strand cDNA Synthesis Kit (NZYTech). Quantitative PCR assays and primer design (Table 1) were performed as described by Machado et al. (24). The expression of the target gene was normalized using the average expression of European seabass elongation factor 1α (ef1α) and the 40s ribosomal protein (40s). The target genes were selected according to the goal of each trial, direct immune mechanisms or apoptosis signaling. PCR efficiency and relative expression ratio of target gene in experimental groups versus those in control groups were calculated according Pfaffl method (50).
Table 1 Forward and reverse primers for real-time PCR.
Statistical Analysis
All results are expressed as mean ± standard deviation (mean ± SD). Data were analyzed for normality (Shapiro-Wilk’s W test) and homogeneity of variance (Levene’s test) and, when necessary, transformed before being treated statistically. Data were analyzed by one-way (MTT assay) or multifactorial ANOVA, with AA, time, and stimulus as factors, and followed by Tukey post-hoc test to identify differences between the experimental treatments. All statistical analyses were performed using the computer package STATISTICA 12 for WINDOWS. The level of significance used was p ≤ 0.05 for all statistical tests.
Results
MTT Assay
After 24 h incubation of HKL with the different AA concentrations, the cell viability of the leucocytes cultured with M2x was increased compared to the control (L-15) as indicated by the different lower case letters in Figure 2. Tryptophan treatments (T1x and T2x) failed to alter HKL viability compared do L-15.
Figure 2 Cell viability after 24 h incubation with the different AA treatments. Values are presented as means ± SD (n = 12). P-values from one-way ANOVA (p-value = 0.001). Tukey post hoc test was used to identify differences in the experimental treatments. Different letters indicate differences among AA treatments.
Immune Response
ATP Production
All AA treatments presented higher ATP concentrations in response to PhdpUV compared to Ø and LPSPhdp after 4 h while at 24 h of incubation, only L-15 cells displayed higher ATP when incubated with PhdpUV than those incubated with LPSPhdp (capital letters in Figure 3). Methionine-treated cells (M1x and M2x) failed to alter ATP production compared to the control medium (L-15). Nevertheless, and as previously described ATP concentration was significantly increased in both methionine doses (M1x and M2x) in response to PhdpUV compared to the remaining stimulus at 4 h, with this production significantly decreasing at 24 h for the M1x. Similarly to methionine treatments, both T1x and T2x failed to increase ATP production in response to LPSPhdp compared to Ø whereas an increase of its production in response to PhdpUV at 4 h was observed. In fact, the higher tryptophan dose (T2x) showed the same pattern (increase of ATP production in response to PhdpUV compared to Ø) after 24 h of incubation. Finally, as pointed by the different lower case letters, T1x and T2x incubated for 4 h with PhdpUV presented a lower ATP concentration than cell culture in L-15 at the same time and stimuli.
Figure 3 Extracellular ATP concentration in the supernatant of HKL subjected to the experimental treatments. Values are presented as means ± SD (n = 6). P-values from multifactorial ANOVA (p-value < 0.001). Tukey post hoc test was used to identify differences between the experimental treatments. Different low case letters indicate differences among AA treatments at the same time and stimuli, while capital letters denote statistically significant differences between stimuli, within the same AA treatment, at the same time. An asterisk indicates differences between times with the same stimulus.
TAC Concentration
Results on TAC, presented in the Figure 4, were organized by stimulus contrary to the previous figure in order to properly point to the observed difference. A single significant increase in the total antioxidants was observed in the supernatant of HKL subjected to PhdpUV, regardless of exposure time and AA treatment, compared to the remaining stimulus.
Figure 4 Extracellular TAC (total antioxidants concentration) in the supernatant of HKL subjected to the experimental treatments. Values are presented as means ± SD (n = 6). P-values from multifactorial ANOVA (p-value < 0.001). Tukey post hoc test was used to identify differences in the experimental treatments. Capital letters denote statistically significant differences between stimuli, within the same AA treatment, at the same time.
Polyamines Concentration
Since methionine has a recognized role in the polyamine biosynthesis pathway and no direct effect of tryptophan is expected, the assay was only performed in cells incubated with L-15, M1x, and M2x after 48 h stimulation with PhdpUV or unstimulated (Ø) (Figure 5). In the absence of an immune stimulus (Ø) cells cultured with M2x showed the ability to increased polyamine production compared to L-15, while M1x failed to do so (lower case letters). Besides that, upon immune stimulation by PhdpUV incubation for 48 h, both methionine doses, M1x and M2x, showed a higher polyamine production than those incubated in the standard medium, L-15.
Figure 5 Extracellular polyamines concentration in the supernatant of HKL subjected to the experimental treatments. Values are presented as means ± SD (n = 6). P-values from multifactorial ANOVA (p-value = 0.048). Tukey post hoc test was used to identify differences in the experimental treatments. Different low case letters indicate differences among AA treatments at the same stimuli, while capital letters denote statistically significant differences between stimuli within the same AA treatment.
NO Production
Nitric oxide production is presented in Figure 6. The NO production in response to the different stimuli was modulated in both methionine doses. Both methionine treatments, M1x and M2x, presented higher NO production in response to PhdpUV than L-15 treatment, regardless of incubation time, while tryptophan failed to show any alterations compared to L-15 (lower case letters). In fact, in response to PhdpUV and regardless time of exposure, M1x enhanced NO concentration compared to Ø, while M2x-treated cells and stimulated with PhdpUV showed increased NO production compared to both Ø and LPSPhdp (capital letters).
Figure 6 Extracellular nitric oxide concentration in the supernatant of HKL subjected to the experimental treatments. Values are presented as means ± SD (n = 6). P-values from multifactorial ANOVA (p-value = 0.009). Tukey post hoc test was used to identify differences in the experimental treatments. Different low case letters indicate differences among AA treatments while capital letters denote differences between stimuli.
Gene Expression
Gene expression results are presented in Supplementary Table 1. In response to stimuli, the mRNA transcripts of il1β and dnmt1 were up-regulated in HKL exposed to PhdpUV compared to the remaining stimulus, regardless of AA treatment and time
When looking to the methionine treatments, the highest medium supplementation (M2x) led to an increase of the overall expression of dnmt1 when compared to the reaming AA treatments and disregarding stimuli or time of exposure (Figure 7A). Also, in response to PhdpUV, M2x treated-cells presented a significant up-regulation of tnfα (Figure 7B) and odc (Figure 7C) compared to both L-15 and M1x (lower case letters). In fact, this cells (M2x-cultured cells exposed to PhdpUV, regardless time) presented a significantly higher expression of tnfα and odc compared to LPSPhdp or Ø, respectively (capital letters). Methionine surplus (M1x and M2x) also increased sms (Figure 7D) mRNA expression when stimulated with LPSPhdp, compared to L-15. Also, the same treatments (M1x and M2x LPSPhdp) presented an improved expression compared to both unstimulated (Ø) and PhdpUV (capital letters).
Figure 7 Quantitative expression of (A) DNA methyltransferase 1 (p-value = 0.003), (B) tumor necrosis factor α (p-value = 0.001), (C) ornithine decarboxylase (p-value = 0.028), (D) spermine synthase (p-value <0.001), (E) interleukin 10 (p-value= 0.037), (F) arginase 2 (p-value < 0.001) and (G) indoleamine dioxygenase 2 (p-value < 0.001) in HKL subjected to the experimental treatments. Values are presented as means ± SD (n = 6). Multifactorial ANOVA was followed by Tukey post hoc test was used to identify differences in the experimental treatments. Different low case letters indicate differences among AA treatments while capital letters denote statistically significant differences between stimuli. An asterisk indicates differences between times.
Regarding tryptophan medium supplementation, HKL showed an up-regulation of the anti-inflammatory gene il10 (Figure 7E) with the higher tested dose (T2x) presenting increased expression compared to M1x and M2x. However, as perceived by the different capital letters in Figure 7F, the highest tryptophan dose, T2x, up-regulated arg2 transcripts in response to PhdpUV compared to the remaining AA treatments, and its unstimulated and LPSPhdp counterparts (capital letters). Additionally, T2x-treated cells showed an increase in time of ido2 (Figure 7G) expression in response to PhdpUV with a significantly higher expression compared to all the remaining AA treatments (lower case letters) and its equivalents stimulated with LPSPhdp and Ø after a 24 h incubation (capital letters).
Apoptotic Response
Amino Acids on AIP56 Cleaving Activity of the p65 Subunit
A total of four fish were used to test the activity of the AIP56 in the presence of the highest AA treatments by the evaluation of the p65 cleavage, as presented in Figure 8. Similarly to L-15, both M2x and T2x did not hampered AIP56 activity on p65 of HKL as seen by the lower detection in leucocytes incubated with the toxin. Figure 8 presents the results of two biological replicate.
Figure 8 Example of a western blot of p65 cleavage in HKL lysates subjected to the experimental treatments and incubated for 2 h with Ø (-) or 2 µg ml-1 of AIP56 (+).
Caspase-3 Active
A fold-change of caspase 3 activity relative to the unstimulated cells cultured with L-15 at 1 h was performed and presented in Figure 9. The activity of caspase 3 was evaluated in cells cultured with the different AA concentrations after 1, 3, and 6 h of stimulation with AIP56 or in the absence of the stimulus. No statistical modulation of caspase 3-activity was observed by methionine supplementation compared to L-15 and, despite the clear tendency, the expected increase of caspase 3- activity in response to AIP56 was not observed when compared to Ø, which could be explained by the relative high activity in methionine unstimulated (Ø) treatments (Figure 8). In the case of tryptophan, higher activity of caspase 3 was observed in HKL incubated with both supplementation levels, T1x and T2x, relative to L-15 and regardless of time or stimulus (lower case letters). Moreover, indicated by the capital letters, cells cultured in L-15, T1x, and T2x presented an increase of caspase 3- activity in response to AIP56.
Figure 9 Caspase 3 activity of HKL subjected to the experimental treatments. Values are presented as means ± SD (n = 6). P-values from multifactorial ANOVA (p- value < 0.001). Tukey post hoc test was used to identify differences in the experimental treatments. Different low case letters indicate differences among AA treatments while capital letters denote statistically significant differences between stimuli for the same AA treatment.
Gene Expression
Due to the amount of data resulted from the gene expression, all data regarding is presented in Supplementary table 2 including the main effects of the tested factors and the possible interactions.
In response AIP56 stimuli, was observed a down-regulation of the nf-κβ regardless of AA treatment and time, while increasing the expression of il1β at 1h of exposure, regardless of AA (Supplementary Table S2). Additionally, L-15- incubated cells showed increased casp3 expression at 3 h in response to AIP56 (Figure 10A), compared to Ø at the same time. L-15 cells showed increased mtor, amd1, and dnmt3b expression at 3 h compared to 1 and 6 h (Supplementary Table S2).
Figure 10 Quantitative expression of (A) caspase 3 (p-value = 0.011), (B) nuclear factor kappa B (p-value = 0.012), (C) interleukin 8 (p-value 0.015), (D) mechanistic target of rapamycin (p-value < 0.001), (E) interleukin 1 β (p-value = 0.032), (F) transcription factor p65 (p-value < 0.011), (G) arylformamidase (p-value < 0.025), (H) DNA (cytosine-5-)-methyltransferase 3 beta (p-value < 0.026) and (I) caspase 8 (p-value < 0.011), in HKL subjected to the experimental treatments. Values are presented as means ± SD (n = 6). Multifactorial ANOVA was followed by Tukey post hoc test was used to identify differences in the experimental treatments. Different low case letters indicate differences among AA treatments while capital letters denote statistically significant differences between stimuli. Symbols indicate differences between times.
A general increase in the expression of pro-inflammatory genes, as il1β, nf-κb, and il8 was found in response to methionine medium supplementation. Irrespective of stimuli, the expression of the pro-inflammatory signals nf-κb (Figure 10B) and il8 (Figure 10C) was higher in M1x and M2x after 3 h, respectively, compared to L-15 and with both genes presenting a peak of expression at 3 h. M2x also showed higher amd1 at 3 h, regardless of stimuli, and mtor was also found higher in M1x-treated cells at 3 h (Figure 10D). In response to AIP56, both methionine supplementation levels (M1x and M2x) allowed HKL to increase il1β (Figure 10E) transcripts compared to L-15 while decreasing the expression of casp3 at 3 h (Figure 10A).
HKL incubated in a rich-tryptophan medium showed modulation of key apoptotic, catabolism, and nutrient sensing-related genes. Regardless of stimuli or incubation time, the expression of p65 (Figure 10F) and afmid (Figure 10G) were down-regulated in both tryptophan levels and T1x, respectively, relative to L-15, while dnmt3b (Figure 10H) expression was down-regulated specifically at 3 h. Also, unstimulated (Ø) HKL cultured with T2x showed lower sms mRNA expression than HKL cultured with T1x and L-15 (Supplementary Table S2). Moreover, T2x showed decreased amd1 expression at 3 h and increased mtor expression at 6 h, which presented a peak of expression at that time (Supplementary Table S2). In response to AIP56, casp3 (Figure 10A) transcripts were down-regulated at 3 h in T1x and T2x compared to L-15, while casp8 (Figure 10I), was found increased in T1x at 6 h incubation with AIP56 compared to all treatments.
Discussion
The potential of methionine and tryptophan supplementation in the response of HKL upon immune stimulation with LPS-extracted and UV-inactivated Phdp was studied in vitro. Moreover, the HKL apoptosis instigated by AIP56 toxin was evaluated. The following discussion was assembled in order to individually debate each AA effect on the direct immune mechanism in response to the stimulus, on the AA-related pathways with close association with the innate mechanisms, and apoptotic signals.
The present study showed that, regardless of AA treatment, cell immune responses were not triggered following exposure to LPSPhdp. Most changes were observed in response to PhdpUV challenge, both at functional and transcriptional levels. Indeed, cultured cells exposed to LPSPhdp exhibited only one difference compared to the unstimulated cells in an AA surplus scenario (discussed later) while being generally surpassed by the PhdpUV effect. In response to PhdpUV, HKL increased il1β and dnmt1 expressions, regardless AA treatment. IL1β is the key mediator of the inflammatory response produced by activated macrophages (51) and DNMT1 is an enzyme that catalyzes the transfer of methyl groups derived from SAM to specific CpG structures of the DNA regulating gene expression (18). Together with il1β and dnmt1 mRNA expressions, an increase of extracellular ATP and antioxidant concentrations (TAC) was observed in the HKL cultured in standard L-15 in response to PhdpUV comparatively to LPSPhdp. Increasing levels of extracellular ATP and antioxidant production are expected during inflammatory conditions (52, 53) since ATP acts as an inflammatory mediator during inflammation in macrophages (53). Also, antioxidants production are increased in response to inflammatory stimuli as a direct response to the enhanced production and release of reactive oxygen species (52). Likewise, the absence of pro-inflammatory indicators increment in response to LPSPhdp compared to the PhdpUV may point to other bacterial components rather than LPS that may be responsible for the observed response. Actually, the expected level of LPS within the PhdpUV inoculum at a concentration of 1 × 106 CFU ml-1 was 0.006 µg ml-1, a value significantly lower than the 10 µg ml-1 LPS inoculum in LPSPhdp. Additionally, LPS recognition mechanisms by most teleost fish are still unknown, and there seems to be a lack of membrane receptor (i.e. Toll-like receptor) able to recognize LPS and induce inflammation (54). Indeed, Bi et al. (55) proposed the use of other strategies, such as outer membrane vesicles produced by Gram-negative bacteria, to serve as vehicle for LPS introduction to the intracellular host environment. These authors observed that, similarly to mammals, fish cytoplasmic NOD1 receptor is able to recognize LPS activating the NF- κB signal pathway and concomitant expression of pro-inflammatory signals. Hence, the limited effects observed in the present work upon purified LPS cell-stimulation could be explained by the lack of an intermediary vehicle to deliver LPS into the cell cytosol (56).
AIP56 is an exotoxin secreted by virulent Phdp and induces apoptotic macrophages death (57), impairing the host’s phagocytic capacity. Moreover, NF-κB, a key transcriptional factor in the initiation of inflammation (58), is the central target of cleavage by AIP56 (49). In the present work, the effectiveness of the toxin regardless AA treatment was confirmed by Western blot that displayed AIP56 ability to cleave the NF- κB- p65 subunit, together with a significant reduction of nf-κb expression.
Methionine
In the present study, cultured cell viability was improved after 24 h incubation with a medium containing two times more methionine than the L-15 medium. The role of methionine in polyamine biosynthesis (19) has been proven to enhance European seabass leucocyte proliferation and response to infection in vivo (11, 14). Nonetheless, since proliferation and differentiation capacity of the present HKL cultured cells is very limited or even absent, increased viability strictly point to a potential improvement of cell fitness. A noteworthy finding is that both methionine supplementation levels led to an increase of polyamines cellular content after 48 h incubation period in response to PhdpUV. Moreover, the highest methionine supplementation level (i.e. M2x) presented increased polyamine content even in the absence of stimulus, together with the up-regulation of dnmt1, an enzyme that has a key role in the regulation of gene expression (18). In fact, recent in vivo study performed in European seabass juveniles (14) point to methionine surplus ability to increase the concentration of circulating leucocytes and neutrophils after 15 days of feeding. This supports the methionine-availability aptitude to modulate both aminopropylation (18) and methylation pathways (19) in the absence of immune stimuli.
Nevertheless, in response to an immune challenge, as LPSPhdp, both methionine supplementation levels improved sms mRNA expression. Spermine synthase, coded by sms, is an enzyme responsible for the conversion of polyamine spermidine into spermine. Moreover, when the immune insult was PhdpUV, HKL cultured in methionine-rich medium (M2x) were able to increase odc expression. Ornithine decarboxylase, coded by odc, is responsible for decarboxylation of ornithine to putrescine in the polyamine pathway also in macrophages (59). Also, an increase of tumor necrosis factor, tnfα, was observed. TNFα presents critical cell functions in cell proliferation, survival, differentiation, and apoptosis, with macrophages as major producers (60). It is then hypothesized that, together with an improvement of immune functions, modulation of methionine-related pathways, more precisely the aminopropylation and methylation routes, were stimulated. This agrees with previous in vivo studies that demonstrated an improvement of cellular immune status and immune response following an inflammatory insult, with modulation of the methionine-related polyamine biosynthesis pathway (11, 14). Moreover, both methionine-supplementation levels led to an improvement of NO production in response to inactivated bacteria (PhdpUV) compared to the control medium. Also, M1x and M2x were the only treatments that increased NO production in response to both unstimulated and LPSPhdp groups. As previously observed by Azeredo et al. (16) in response to UV-inactivated Vibrio anguillarum, the increased NO production in response to PhdpUV could be related to methionine ability to indirectly modulate respiratory burst mechanisms. As cysteine precursor, and consequently precursor of the free radical scavenger glutathione, methionine could have an important role in redox potential modulation (9).
When the apoptotic mechanisms were induced by the bacterial exotoxin AIP56 (57), methionine supplementation led to a down-regulation of casp3 compared to the control after 3 h of stimulus, in spite of overall high caspase 3- activity (non-significant). Despite that, the decreased expression of casp3 was accompanied by the higher expression of nf-κb in M1x-cultured cells at 3 h, regardless of stimulus. Caspase 3 is an apoptotic executioner caspase, triggered by the resulting chain reaction of the formerly activated initiator caspases (e.g. caspases 8 and 9) (61). Also, as previously discussed, NF-κB cleavage by AIP56 action (49) and may impair key inflammatory mechanisms such as the transcription of DNA and cytokine production (58), leucocyte recruitment, and cell survival (62). Knowing that in vitro methionine deprivation induces apoptosis (63, 64), it was considered that by the improvement of overall cell fitness, sustained by the increase of cell viability, polyamine content, NO production and increased expression of TNFα as well as methionine metabolism-related genes in response to and immune stimuli (LPSPhdp or PhdpUV), methionine supplementation may have contributed to the decrease of apoptotic signals, possibly alleviating AIP56-induced apoptosis signals. In fact, the expression of the cytokine IL1β, a pro-inflammatory cytokine induced by the NF-κB (39), was found increased in response to AIP56, showing signs of higher activity of the transcription factor.
Overall, present results point to an improvement of HKL immune response by methionine medium supplementation, mostly at the highest supplementation level (i.e. 1.5 mM). It is then proposed that the effects observed in recent in vivo works, where dietary methionine supplementation was able to enhance European seabass immune status and inflammatory machinery (11, 12, 65), rely on the amelioration of the pathways related to methionine catabolism, with a strict relationship with the leucocyte response, as the aminopropylation (18) and methylation pathways (19). Finally, the overall improved cell status in the methionine-supplemented medium seems to be in accordance with the protection against the apoptotic agent AIP56, and could be essential for the improvement of disease resistance against Phdp, as previously observed by Machado et al. (14).
Tryptophan
Despite the tendency to reduce, the culture-medium supplementation of tryptophan during 24 h did not affect cell viability. Tryptophan involvement in the immune system relies mostly on the suppressor role of its metabolites, and despite a reduction of NO production was expected (16, 66), only a reduction of the extracellular ATP was detected in response to PhdpUV. The ATP released by the inflammatory cells acts as a pro-inflammatory autocrine/paracrine purinergic signal (67) and, by tryptophan supplementation, this indicator was reduced. Macrophages can be differentiated into distinct groups according to not only the inductor of differentiation but also to the inflammation stage and perceived signals (30, 35). Commonly baptized as SHIP [Sample, Heal (M2), Inhibit (M1), and Present (antigen)] (33), macrophages present some plasticity regarding their state, and type 2 macrophages (M2) are associated with the healing and repair phase of the inflammation. In the present study, HKL cultured in tryptophan enriched environment expressed more M2/repair type genotype, as suggested by the increased expression of arginase 2 (arg2) in response PhdpUV. Also, despite non-significant, a tendency to increase the expression of the anti-inflammatory cytokine interleukin 10 (il10) in response to LPSPhdp of T2x-treatmed cells compared to L-15 was observed. Polarized M2 macrophages are known to produce large quantities of il10 (35, 68) and ornithine generated from arginase is associated with M2 phenotype (31). Despite contradictory, the specific function of the IDO enzyme is believed to be anti-inflammatory, as reviewed by Yang and Ming (69). Accordingly, in the present study, changes in the expression of ido2 were also perceived. The indoleamine dioxygenase 2 enzyme mediates tryptophan catabolism by the kynurenine pathway in macrophages and relies on both tryptophan availability (5) and induction by an inflammatory stimulus (25). Thus, as expected, ido2 was up-regulated in the higher tryptophan medium (T2x) after 24 h exposure to PhdpUV while LPSPhdp failed to induce expression.
In response to AIP56, cells cultured in tryptophan-supplemented medium (both T1x and T2x) presented an increase of caspase 3 activity relative to the control cells (L-15 medium cultured HKL). Curiously, the expression of casp3, an executioner caspase, was down-regulated relative to L-15 at 3 h of stimulus, while expression of mtor, which is involved in cell proliferation, was induced at 6 h in T2x-culture cells. It can be speculated that the apoptotic mechanisms were empowered by tryptophan surplus since, together with caspase 3 activity, the initiator caspase 8 expression increased at 6 h in cells cultured with T1x. The immunosuppressive role of tryptophan surplus is further supported by the observed down-regulation of amd1 (19), sms, and dntm3b (18), which are genes with key roles in the support of cell proliferation and differentiation. Moreover, the expression of the target of AIP56 cleavage associated protein, the p65 subunit, which is involved in the translocation and activation of NF-κB, was also down-regulated by tryptophan supplementation. Despite most differences presented in this study included both unstimulated and AIP56-stimulated cells, results seem to point to some level of aggravation of cell capacity to respond to AIP56 by tryptophan surplus.
Tryptophan supplementation above the level present in the L-15 medium, points to an attenuated inflammatory response, mostly sustained in the heal/repair extend of the immune system. Despite the lack of changes in the modulation of genes related to AA pathways, it is hypothesized that those mechanisms could have been prompted to sustain the M2/healing type of response to both LPSPhdp and PhdpUV. Some recent in vivo evidence indicates that the dietary supplementation of tryptophan in European seabass compromises leucocytes’ inflammatory response to UV-inactivated (11–13) and live Phdp, ultimately jeopardizing fish disease resistance to the pathogen (24). This is in agreement with the general increase of apoptotic indicators and compromised immune response to AIP56 in the cultured cells.
An Integrated View of the Different Roles of Methionine and Tryptophan
The range of metabolic pathways that are dependent on a proper supply of specific AA unveils their importance in the support of metabolism and health (70). Immune homeostasis, which comprises host capacity to recognize, properly respond, and repair, relies on the adequate supply of specific AA. All these mechanisms are highly controlled and each pathway is initiated or inhibited according to numerous perceived signals. Nonetheless, specific AA can have a lead role in the pro-inflammatory part of the event (e.g. methionine) while others seem to play a more important role in the resolution of inflammation (e.g. tryptophan), presenting both the same importance in the overall immune response.
On the one hand, this was evident in the present study with methionine improving cell viability and polyamine production necessary for cell proliferation (19). These observations were accompanied by the increased expression of pro-inflammatory and methionine-related pathways indicators. With the increased expression of DNMT1 and up-regulation of sms and odc, the modulation of the methylation and aminopropylation pathways, respectively, are displayed. Finally, improved cell responses to an inflammatory agent were accompanied by lower signals of apoptosis by AIP56 with higher impression of pro-inflammatory indicators compared to the control treatment.
On the other hand, immune tolerance is of great importance, specifically in the limitation of self-damage and tryptophan seems to present a key role in such response. Most tryptophan-dependent pathways associated to the immune system are related to the assemblage of anti-inflammatory machinery. In macrophages, tryptophan consumption through the kynurenine pathway is catalyzed by IDO (71). In fact, IDO2 expression was found increased by tryptophan surplus and seemed to have induced signs of macrophages anti-inflammatory phenotype (i.e. high expression of arginase 2, arg2, in response to LPSPhdp) (68). Likewise, when submitted to AIP56 induced-apoptosis, cultured cells incubated with tryptophan presented increased signs of apoptosis and reduced expression of a critical regulator of immune and inflammatory responses (i.e. NF-κB P65), as well as proliferation and differentiation indicators (e.g. SMS, AMD1).
To conclude, in the present study it was specifically showed that methionine and tryptophan have their distinct roles in immune response, with different and contrasting outcomes by the modulation of individual key pathways. Methionine seems to positively contribute to the progress of inflammation, improving the underlying mechanisms activated in response to an inflammatory agent and lowering signals of apoptosis by AIP56, whereas tryptophan seems to presented a clear role in the tolerance process responsible for restriction of the pro-inflammatory cluster of the immune response. This is supported by the several signals of an attenuated inflammatory response to PhdpUV and lowered cell resilience to AIP56.
Data Availability Statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
Ethics Statement
The animal study was reviewed and approved by the CIIMAR Animal Welfare Committee, carried out in a registered installation (N16091.UDER).
Author Contributions
MM and BC conceived the experiments and MM conducted the experimental trials. CS purified the LPSPhdp. MM wrote the manuscript under the supervision of AO-T, CS, and BC. All authors contributed to the article and approved the submitted version.
Funding
This work was partially supported by UIDB/04423/2020, UIDP/04423/2020 and INFLAMMAA (reference PTDC/CVT-CVT/32349/2017), financed by Portugal and the European Union through FEDER and COMPETE 2020, and national funds through Fundação para a Ciência e a Tecnologia (FCT, Portugal). MM and BC were supported by FCT, Portugal (SFRH/BD/108243/2015 and IF/00197/2015, respectively).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
The authors would like to acknowledge Dra. Ana do Vale and Dr°. Nuno dos Santos (i3S/IBMC) for the kindly providing the AIP56 toxin and Dr°. Johnny Lisboa (i3S/IBMC) and Dra. Cassilda Pereira (i3S/IBMC) for all the assistance in the Western blot protocol.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2021.660448/full#supplementary-material
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Keywords: amino acids, inflammation, fish, AIP56, Photobacterium damselae subsp. piscicida
Citation: Machado M, Serra CR, Oliva-Teles A and Costas B (2021) Methionine and Tryptophan Play Different Modulatory Roles in the European Seabass (Dicentrarchus labrax) Innate Immune Response and Apoptosis Signaling—An In Vitro Study. Front. Immunol. 12:660448. doi: 10.3389/fimmu.2021.660448
Received: 29 January 2021; Accepted: 25 February 2021;
Published: 15 March 2021.
Edited by:
Felipe E. Reyes-López, Universitat Autònoma de Barcelona, SpainReviewed by:
Chunxiao Zhang, Jimei University, ChinaMorgane Henry, Hellenic Centre for Marine Research (HCMR), Greece
Carlo C. Lazado, Fisheries and Aquaculture Research (Nofima), Norway
Elisabeth Holen, Norwegian Institute of Marine Research (IMR), Norway
Copyright © 2021 Machado, Serra, Oliva-Teles and Costas. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Marina Machado, mcasimiro@ciimar.up.pt; Benjamín Costas, bcostas@ciimar.up.pt