Hiroki Takeuchi
Eriko Nakamura2
Atsuo Amano- 1Department of Preventive Dentistry, Osaka University Dental Hospital, Suita, Japan
- 2Department of Preventive Dentistry, Graduate School of Dentistry, Osaka University, Suita, Japan
Periodontal diseases initiate on epithelial surfaces of the subgingival compartment, while the gingival epithelium functions as an epithelial barrier against microbial infection and orchestrates immune responses. Porphyromonas gingivalis is a major pathogen of periodontal diseases and has an ability to penetrate the epithelial barrier. To assess the molecular basis of gingival epithelial barrier dysfunction associated with P. gingivalis, we newly developed a three-dimensional multilayered tissue model of gingival epithelium with gene manipulation. Using this novel approach, P. gingivalis gingipains including Arg- or Lys-specific cysteine proteases were found to specifically degrade junctional adhesion molecule 1 and coxsackievirus and adenovirus receptor in the tissue model, leading to increased permeability for lipopolysaccharide, peptidoglycan, and gingipains. This review summarizes the strategy used by P. gingivalis to disable the epithelial barrier by disrupting specific junctional adhesion molecules.
Significance Of Porphyromonas gingivalis Infection in Human Gingival Epithelium
Epithelial cells are located on the front line of infection defense, and function as a physical barrier against pathogenic bacteria and their products. The epithelial barrier is formed by cell-cell adhesion, and consists of tight junctions that prevent leakage of transported substances, and seal the paracellular pathway. Human gingival epithelial cells have been reported to express tight-junction associated proteins, such as claudin, occludin, junctional adhesion molecule 1 (JAM1), and zonula occludens-1 [1], among which JAM1, an immunoglobulin superfamily protein, reportedly localizes in mucosal epithelium of numerous organs [2].
Periodontitis is basically an infectious disease that causes destruction of periodontal tissues by interactions between periodontal pathogens and host cells [3]. Since gingival epithelial cells are the first to face periodontal pathogens, gingival epithelial tissues are potentially involved in the pathogenesis and progress of periodontitis. Porphyromonas gingivalis, a Gram-negative anaerobe, is a periodontal pathogen that expresses a variety of virulence factors, such as lipopolysaccharide (LPS), peptidoglycan (PGN), and gingipains. Periodontal diseases are multispecies infections involving pathogenic communities in which P. gingivalis can increase the pathogenicity of the entire multispecies periodontal community [3]. Various studies have shown that P. gingivalis occurrence is significantly associated with initiation of periodontitis, with odds ratios of 11.788 [4], 12.3 [5], and 5.6 [6] reported. It is also known that an increase in amount of “red complex” species, consisting of P. gingivalis, Treponema denticola, and Tannerella forsythia, in subgingival biofilm is related to initiation and progression of periodontitis [7]. A cross-sectional study revealed that P. gingivalis is the most influential pathogen among red complex bacteria [8]. However, it is ethically difficult to analyze the effects of P. gingivalis infection on tight junction-associated proteins using human gingival epithelium specimens. Hence, features of the physiological function related to tight junction-associated proteins in the oral cavity have become an interesting focus of research.
Advantages Of 3D-Tissue Models Of Human Gingival Epithelium
From the standpoint of replacement, reduction, and refinement (3Rs), alternative methods for animal experiments are needed for medical research studies [9]. Physiological tissues are composed of various types of cells and connective tissues, thus how to construct three-tissue models with similar functions in living tissues has been investigated. Within an organism, the extracellular matrix has an important role to regulate the interface-surface structure of host cells. We previously reported that a cell-accumulation technique [10] using fibronectin and gelatin, extracellular matrixes, was useful to re-construct human gingival epithelial tissues [11, 12]. The advantages of this technique include (1) development of healthy human tissues, (2) gene manipulation including overexpression and knockdown, (3) direct measurement of fluorescent-tracer transmission in human tissues, (4) time-course observations of pathological condition before disease onset, and (5) administration of LPS and PGN, for examining PAMPs and infection by P. gingivalis. We have found that 3D-tissue models of gingival epithelium are useful for defining the cause-and-effect relationships of risk factors in terms of elimination of potential confounding factors.
P. gingivalis Gingipains Degrade JAM1 AND CXADR
P. gingivalis secretes Arg- and Lys-specific cysteine proteases, termed Arg-gingipains (RgpA and RgpB) and Lys-gingipain (Kgp), respectively, which are major virulence factors [13, 14]. In a previous study, to clarify which tight junction-associated protein(s) are degraded by P. gingivalis infection, we infected immortalized human gingival epithelial (IHGE) cells [15] with P. gingivlis ATCC 33277 or KDP136, a Δkgp ΔrgpA ΔrgpB mutant [16], for 1 h. Immunoblot and confocal microscopic analyses revealed that P. gingivalis apparently degraded JAM1 and coxsackievirus and adenovirus receptor (CXADR), another JAM-family protein [17], but not claudin 1, claudin 4, E-cadherin, occludin, or zonula occludens-1, in a gingipains-dependent manner [11, 12]. Notably, medium used for culturing P. gingivalis WT, but not that used for a Δkgp ΔrgpA ΔrgpB mutant, also degraded JAM1 and CXADR of IHGE cells, indicating that gingipains function to degrade JAM1 and CXADR.
Specific Degradation Of JAM1 And CXADR BY Gingipains
JAM family proteins have an extracellular domain along with two immunoglobulin-like domains, a single transmembrane domain, and a short cytoplasmic tail with a PDZ-domain-binding motif [18]. Hence, we constructed chimeric proteins of JAM1 and CXADR expressed by IHGE cells, and infected cells with P. gingivalis, after which the responsible residues of JAM1 K134 and R234, and CXADR R145 and K235 were examined for determining gingipains degradation (Figure 1). JAM1 K134 and CXADR R145 are located between the two immunoglobulin domains, while JAM1 R234 and CXADR K235 are set at the N-terminus of the transmembrane domain. A dimerization motif in the N-terminal immunoglobulin domain is essential for JAM1- or CXADR-homodimer formation, thus gingipains efficiently dampen the functions of JAM1 and CXADR.
Figure 1. The residues involved in degradation of JAM1 and CXADR by P. gingivalis gingipains. Schematic view of the JAM1 and CXADR structure in gingival epithelial cells. The K134 and R234 residues of JAM1, and the R145 and K235 residues of CXADR are involved in degradation by P. gingivalis gingipains in gingival epithelial cells. IG-LIKE, immunoglobulin-like domain (blue); TM, transmembrane domain (green).
Fusobacterium nucleatum and Streptococcus gordonii are human oral bacteria that can assemble mixed-species communities [19]. Hence, IHGE cells were infected with F. nucleatum or S. gordonii, and it was confirmed that the protein levels of JAM1 and CXADR were not decreased, thus indicating that F. nucleatum and S. gordonii do not degrade JAM1 and CXADR [11, 12].
Next, 3D-tissue models of gingival epithelium were constructed, and localization of JAM1 and CXADR was confirmed and found to be comparable to that seen in human gingiva. We also found that P. gingivalis WT decreased JAM1 and CXADR even in tissues 3–4 layers below the surface, whereas the Δkgp ΔrgpA ΔrgpB mutant did not [11, 12]. These results indicate that gingipains continuously degrade JAM1 and CXADR, and deeply invade human gingival epithelial tissues.
P. gingivalis Induces Penetration Of LPS and PGN Through Gingival Epithelium
LPS, a gram-negative bacteria endotoxin, and PGN, which exists in a mesh-like pattern outside the plasma membrane of most bacteria, are known as pathogen-associated molecular patterns (PAMPs) that cause initiation of host immune response [20]. In cases with leukocyte adhesion deficiency, one of the syndromes associated with periodontitis [21], LPS in the subepithelial area was reported to be detected in gingival tissues, but not in those from healthy cases [22]. In addition, plasma LPS levels were found to be correlated with multiple clinical parameters of aggressive periodontitis [23] and decreased by periodontal therapy [24]. Hence, we hypothesized that PAMPs from oral bacteria penetrate gingival epithelial tissues.
To assess the contribution of JAM1 expression to the permeability of gingival epithelial cells, 3D-tissue models of gingival epithelium were generated, then permeability assays were performed using fluorescent probe-tagged LPS or PGN in combination with P. gingival infection. To confirm the involvement of JAM1 or CXADR in P. gingivalis-affected permeability, 3D tissues were infected with P. gingivalis using IHGE cells overexpressing JAM1 or CXADR, which were then treated with fluorescent tracers [11, 12]. Thirty minutes after administration, the permeability to LPS or PGN was increased by P. gingivalis infection, whereas that was decreased by JAM1 or CXADR overexpression in gingival epithelial tissues. These results suggest that JAM1 and CXADR degradation by P. gingivalis causes penetration of gingival epithelium by LPS and PGN (Figure 2).
Figure 2. Proposed model of transfer of bacterial virulence factors by P. gingivalis gingipains through gingival epithelium. P. gingivalis gingipains degrade JAM1 and CXADR, leading to increased permeability to gingipains, LPS, and PGN. Subsequently, gingipains become translocated to deeper epithelium for additional degradation of JAM1 and CXADR, thus allowing LPS and PGN to penetrate the gingival epithelium and reach subepithelial tissues.
Discussion
Difference Between Gene Expression and Protein Localization
We confirmed that the immature forms of JAM1 and CXADR possessed a signal peptide and were localized in the endoplasmic reticulum [11, 12]. Generally, the levels of the immature forms of JAM1 and CXADR are proportional to those of the messenger RNA levels. In contrast, P. gingivalis degraded mature forms of JAM1 and CXADR in the plasma membrane, but not the immature forms in IHGE cells. These results suggest that surface protein localization of JAM1 and CXADR is needed to be confirmed in gingival epithelial cells to accurately evaluate the effects of risk factors of periodontitis.
Protein Modification
It has been reported that JAM1 is phosphorylated at Y280 [25] and S284 [26], and glycosylated at N185 [27], while CXADR is glycosylated at N106 and N201 [28]. In general, protein phosphorylation modulates subcellular localization, and N-linked protein glycosylation is involved in cell–cell and cell–extracellular matrix attachment. Hence, elucidation of risk factors of periodontitis that have effects on JAM1- or CXADR-protein modification is considered to helpful to better understand its etiology.
Intracellular Trafficking
The C-terminal cytosolic domain of JAM1 possesses a class II PDZ domain binding motif (-SFLV-COOH) [29]. In cytosolic space, JAM1 is known to associate with various partner proteins via the PDZ domain [30]. We confirmed that the immature forms of JAM1 and CXADR were localized in the endoplasmic reticulum, in which these proteins were apparently digested as a single peptide and N-glycosylated for maturation. To show biological activity, JAM family proteins must be transferred from the endoplasmic reticulum to plasma membrane, in which case regulator proteins may also bind with JAM via the PDZ domain. We recently observed that JAM1 localization in the plasma membrane was not disturbed by actin polymerization inhibitors (unpublished data). In contrast, actin depolymerization has been shown to disturb plasma-membrane localization of claudin-1 and occludin, tight junction proteins [31]. Thus, it is considered that transport of JAM family proteins occurs in a manner different from that of claudin and occludin.
Other Cell Types
JAM was initially identified as a platelet membrane protein [32] and shown to play an important role in platelet assembly [33]. Generally, when blood-vessel walls are damaged, platelets aggregate in the wound and serve to stop bleeding. If the function of platelets is abnormal, a bleeding tendency will develop. To monitor the health or inflammation of gingival tissues, the parameter of bleeding on probing (BOP) has been well documented [34, 35]. Furthermore, a positive correlation between number of periodontal pockets with BOP and serum LPS concentration has been reported [36]. Thus, the molecular mechanisms related to how P. gingivalis affects platelets in the process of periodontal pathogenesis is quite interesting, though difficult to fully understand. Platelets are torn from the cytoplasm of polymorphonuclear giant cells in bone marrow and enter the bloodstream, and lose their nuclei. There are technical limitations when attempting to use human platelets for molecular biological research, such as passage culturing, gene manipulation, bacterial and viral contamination, and cross-contamination with the other cells, as well as confounding factors. Technical developments, including induction of differentiation to anuclear or short lifespan cells, as well as re-construction of human gingival epithelium, are needed in order to fully understand the etiology of periodontitis.
Author Contributions
HT and AA wrote the manuscript. HT, EN, and SY constructed the images. All authors contributed to the article and approved the submitted version.
Funding
This research was supported by JSPS KAKENHI Scientific Research grants (26253094 and 18H04068) (to AA), JSPS KAKENHI Grants-in-Aid for Young Scientists (15K20360 and 17K17083) (to HT), a JSPS KAKENHI Scientific Research grant (19K10085) (to HT), and a JSPS KAKENHI Grant-in-Aid for Young Scientists (Start-up) (21K21038) (to EN), each from the Japan Society for the Promotion of Science. The funders had no role in study design, data collection, preparation of the manuscript, or decision to publish.
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.
Publisher's Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Acknowledgments
We appreciate the technical support related to confocal laser microscopy provided by the Center for Oral Science, Osaka University Graduate School of Dentistry. We also appreciate Harumi Aoki for editing the application form for this clinical study.
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Keywords: periodontitis, Porphyromonas gingivalis, gingipains, gingival epithelium, lipopolysaccharide, peptidoglycan, epithelial barrier, tissue model
Citation: Takeuchi H, Nakamura E, Yamaga S and Amano A (2022) Porphyromonas gingivalis Infection Induces Lipopolysaccharide and Peptidoglycan Penetration Through Gingival Epithelium. Front. Oral. Health 3:845002. doi: 10.3389/froh.2022.845002
Received: 29 December 2021; Accepted: 14 January 2022;
Published: 08 February 2022.
Edited by:
Richard Lamont, University of Louisville, United StatesReviewed by:
Pirkko Pussinen, University of Helsinki, FinlandCopyright © 2022 Takeuchi, Nakamura, Yamaga and Amano. 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: Hiroki Takeuchi, dGFrZXVjaGloJiN4MDAwNDA7ZGVudC5vc2FrYS11LmFjLmpw