AUTHOR=Lantz Benjamin J. , Moriwaki Mika , Oyebamiji Olufunmilola M. , Guo Yan , Gonzalez Bosc Laura 

TITLE=Chronic hypoxia disrupts T regulatory cell phenotype contributing to the emergence of exTreg-TH17 cells

JOURNAL=Frontiers in Physiology

VOLUME=14

YEAR=2024

URL=https://www.frontiersin.org/journals/physiology/articles/10.3389/fphys.2023.1304732

DOI=10.3389/fphys.2023.1304732

ISSN=1664-042X

ABSTRACT=<p>The imbalance between pro-inflammatory T helper 17 (T<sub>H</sub>17) cells and anti-inflammatory regulatory T cells (Tregs) has been implicated in multiple inflammatory and autoimmune conditions, but the effects of chronic hypoxia (CH) on this balance have yet to be explored. CH-exposed mice have an increased prevalence of T<sub>H</sub>17 cells in the lungs with no change in Tregs. This imbalance is significant because it precedes the development of pulmonary hypertension (PH), and T<sub>H</sub>17 cells are a major contributor to CH-induced PH. While Tregs have been shown to attenuate or prevent the development of certain types of PH through activation and adoptive transfer experiments, why Tregs remain unable to prevent disease progression naturally, specifically in CH-induced PH, remains unclear. Our study aimed to test the hypothesis that increased T<sub>H</sub>17 cells observed following CH are caused by decreased circulating levels of Tregs and switching of Tregs to exTreg-T<sub>H</sub>17 cells, following CH. We compared gene expression profiles of Tregs from normoxia or 5-day CH splenocytes harvested from Foxp3<sup>tm9(EGFP/cre/ERT2)Ayr</sup>/J x Ai14-tdTomato mice, which allowed for Treg lineage tracing through the presence or absence of EGFP and/or tdTomato expression. We found Tregs in CH exposed mice contained gene profiles consistent with decreased suppressive ability. We determined cell prevalence and expression of CD25 and OX40, proteins critical for Treg function, in splenocytes from Foxp3<sup>tm9(EGFP/cre/ERT2)Ayr</sup>/J x Ai14-tdTomato mice under the same conditions. We found T<sub>H</sub>17 cells to be increased and Tregs to be decreased, following CH, with protein expression of CD25 and OX40 in Tregs matching the gene expression data. Finally, using the lineage tracing ability of this mouse model, we were able to demonstrate the emergence of exTreg-T<sub>H</sub>17 cells, following CH. These findings suggest that CH causes a decrease in Treg suppressive capacity, and exTregs respond to CH by transitioning to T<sub>H</sub>17 cells, both of which tilt the Treg–T<sub>H</sub>17 cell balance toward T<sub>H</sub>17 cells, creating a pro-inflammatory environment.</p>