Cell-autonomous Hedgehog signaling controls Th17 polarization and pathogenicity

• Published in: Nature communications Vol. 13; no. 1; p. 4075
• Main Authors: Hanna, Joachim, Beke, Flavio, O’Brien, Louise M., Kapeni, Chrysa, Chen, Hung-Chang, Carbonaro, Valentina, Kim, Alexander B., Kishore, Kamal, Adolph, Timon E., Skjoedt, Mikkel-Ole, Skjoedt, Karsten, de la Roche, Marc, de la Roche, Maike
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 14.07.2022; Nature Publishing Group; Nature Portfolio
• Subjects: 13; 13/1; 13/106; 13/31; 13/51; 14/19; 38; 38/35; 38/39; 38/91; 45/88; 45/90; 631/250/1619/554/1898; 631/250/1619/554/1898/1273; 631/250/2152/1566/2493; 631/80/86/2370; 64; 64/60; 96; 96/21; Ablation; Adult; Animal models; Animals; Autoimmune diseases; CD4 antigen; Cell fate; Colitis, Ulcerative - drug therapy; Colitis, Ulcerative - genetics; Embryogenesis; Embryonic growth stage; Hedgehog protein; Hedgehog Proteins - genetics; Hedgehog Proteins - metabolism; Helper cells; Humanities and Social Sciences; Humans; Inflammatory bowel disease; Inflammatory bowel diseases; Intestine; Ligands; Lymphocytes; Lymphocytes T; Mice; multidisciplinary; Pathogenicity; Pathogens; Pattern formation; Polarization; Science; Science (multidisciplinary); Signal Transduction; Signaling; Th17 Cells; Therapeutic targets; Ulcerative colitis; Virulence
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-022-31722-5

Th17 cells are key drivers of autoimmune disease. However, the signaling pathways regulating Th17 polarization are poorly understood. Hedgehog signaling regulates cell fate decisions during embryogenesis and adult tissue patterning. Here we find that cell-autonomous Hedgehog signaling, independent of exogenous ligands, selectively drives the polarization of Th17 cells but not other T helper cell subsets. We show that endogenous Hedgehog ligand, Ihh, signals to activate both canonical and non-canonical Hedgehog pathways through Gli3 and AMPK. We demonstrate that Hedgehog pathway inhibition with either the clinically-approved small molecule inhibitor vismodegib or genetic ablation of Ihh in CD4 +  T cells greatly diminishes disease severity in two mouse models of intestinal inflammation. We confirm that Hedgehog pathway expression is upregulated in tissue from human ulcerative colitis patients and correlates with Th17 marker expression. This work implicates Hedgehog signaling in Th17 polarization and intestinal immunopathology and indicates the potential therapeutic use of Hedgehog inhibitors in the treatment of inflammatory bowel disease. Th17 cells are critical players in the immunopathology of a range of autoimmune diseases. Here the authors implicate Hedgehog signaling in Th17 polarization and in the immunopathology of intestinal inflammation in murine models and suggest therapeutic targeting of Hedgehog signaling in the context of inflammatory bowel disease.