T-cell dysregulation and inflammatory process in Gcn2 ( Eif2ak4 -/- )-deficient rats in basal and stress conditions

• Published in: American journal of physiology. Lung cellular and molecular physiology 2023-05, Vol.324 (5), p.L609-L624
• Main Authors: Bignard, Juliette, Atassi, Fabrice, Claude, Olivier, Ghigna, Maria-Rosa, Mougenot, Nathalie, Abdoulkarim, Bahgat Soilih, Deknuydt, Florence, Gestin, Aurélie, Monceau, Virginie, Montani, David, Nadaud, Sophie, Soubrier, Florent, Perros, Frédéric
• Format: Article
• Language: English
• Subjects: Amino acids; Animals; Apoptosis; Asparaginase; Asparagine; Cell activation; Cellular stress response; Deprivation; Flow cytometry; Glutamine; Homeostasis; Hypertension; Hypertension, Pulmonary; Infiltration; Inflammation; Innate immunity; Kinases; Leukocytes (neutrophilic); Life Sciences; Lung - metabolism; Lung diseases; Lungs; Lymphocytes T; Protein Serine-Threonine Kinases - genetics; Protein Serine-Threonine Kinases - metabolism; Pulmonary Veno-Occlusive Disease - genetics; Rats; RNA, Messenger; Veno-occlusive disease; Western blotting
• ISSN: 1040-0605; 1522-1504
• DOI: 10.1152/ajplung.00460.2021

Hereditary pulmonary veno-occlusive disease (hPVOD) is a severe form of autosomal recessive pulmonary hypertension and is due to biallelic loss of function of the gene (alias 2) coding for GCN2. GCN2 is a stress kinase that belongs to the integrated stress response pathway (ISR). Three rat lines carrying biallelic mutation were generated and found phenotypically normal and did not spontaneously develop a PVOD-related disease. We submitted these rats to amino acid deprivation to document the molecular and cellular response of the lungs and to identify phenotypic changes that could be involved in PVOD pathophysiology. rat lungs were analyzed under basal conditions and 3 days after a single administration of PEG-asparaginase (ASNase). Lung mRNAs were analyzed by RNAseq and single-cell RNAseq (scRNA-seq), flow cytometry, tissue imaging, and Western blots. The ISR was not activated after ASNase treatment in rat lungs, and apoptosis was increased. Several proinflammatory and innate immunity genes were overexpressed, and inflammatory cells infiltration was also observed in the perivascular area. Under basal conditions, scRNA-seq analysis of rat lungs revealed increases in two T-cell populations, a LAG3 T-cell population and a proliferative T-cell population. Following ASNase administration, we observed an increase in calprotectin expression involved in TLR pathway activation and neutrophil infiltration. In conclusion, under basal and asparagine and glutamine deprivation induced by asparaginase administration, rats display molecular and cellular signatures in the lungs that may indicate a role for in immune homeostasis and provide further clues to the mechanisms of hPVOD development.