Gα12 and endoplasmic reticulum stress-mediated pyroptosis in a single cycle of dextran sulfate-induced mouse colitis

• Published in: Scientific reports 2024-03, Vol.14 (1), p.6335-14, Article 6335
• Main Authors: Tak, Jihoon, An, Quanxi, Lee, Sang Gil, Lee, Chang Hoon, Kim, Sang Geon
• Format: Article
• Language: English
• Subjects: 631/337; 631/45; 692/53; 692/699; Animals; Caspase-1; Cell death; Colitis; Colitis - metabolism; Colitis - pathology; Dextran; Dextran sulfate; Dextran Sulfate - toxicity; Disease Models, Animal; Endoplasmic reticulum; Endoplasmic Reticulum Stress; Endoribonucleases - genetics; Endoribonucleases - metabolism; ER stress; Gastrointestinal tract; GTP-Binding Protein alpha Subunits, G12-G13 - metabolism; Gα12/Gα13; Humanities and Social Sciences; IL-1β; Inflammatory bowel disease; Inflammatory bowel diseases; Inflammatory Bowel Diseases - metabolism; Inflammatory Bowel Diseases - pathology; Mice; Mice, Inbred C57BL; mRNA; multidisciplinary; Necroptosis; Protein Serine-Threonine Kinases - genetics; Protein Serine-Threonine Kinases - metabolism; Pyroptosis; Science; Science (multidisciplinary); Sulfates
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-56685-z

Inflammatory bowel disease (IBD) pathogenesis involves complex inflammatory events and cell death. Although IBD involves mainly necrosis in the digestive tract, pyroptosis has also been recognized. Nonetheless, the underlying basis is elusive. Gα12/13 overexpression may affect endoplasmic reticulum (ER) stress. This study examined how Gα12/13 and ER stress affect pyroptosis using dextran sulfate sodium (DSS)-induced colitis models. Gα12/13 levels were increased in the distal and proximal colons of mice exposed to a single cycle of DSS, as accompanied by increases of IRE1α, ATF6, and p-PERK. Moreover, Il-6 , Il-1β , Ym1 , and Arg1 mRNA levels were increased with caspase-1 and IL-1β activation, supportive of pyroptosis. In the distal colon, RIPK1/3 levels were enhanced to a greater degree, confirming necroptosis. By contrast, the mice subjected to three cycles of DSS treatments showed decreases of Gα12/13, as accompanied by IRE1α and ATF6 suppression, but increases of RIPK1/3 and c-Cas3. AZ2 treatment, which inhibited Gα12, has an anti-pyroptotic effect against a single cycle of colitis. These results show that a single cycle of DSS-induced colitis may cause ER stress-induced pyroptosis as mediated by Gα12 overexpression in addition to necroptosis, but three cycles model induces only necroptosis, and that AZ2 may have an anti-pyroptotic effect.