ORMDL3 regulates NLRP3 inflammasome activation by maintaining ER-mitochondria contacts in human macrophages and dictates ulcerative colitis patient outcome

• Published in: The Journal of biological chemistry 2024-04, Vol.300 (4), p.107120-107120, Article 107120
• Main Authors: Sharma, Jyotsna, Khan, Shaziya, Singh, Nishakumari C., Sahu, Shikha, Raj, Desh, Prakash, Shakti, Bandyopadhyay, Pamela, Sarkar, Kabita, Bhosale, Vivek, Chandra, Tulika, Kumaravelu, Jagavelu, Barthwal, Manoj Kumar, Gupta, Shashi Kumar, Srivastava, Mrigank, Guha, Rajdeep, Ammanathan, Veena, Ghoshal, Uday C., Mitra, Kalyan, Lahiri, Amit
• Format: Article
• Language: English
• Subjects: Animals; Colitis, Ulcerative - genetics; Colitis, Ulcerative - metabolism; Colitis, Ulcerative - pathology; cytokine; Dextran Sulfate - toxicity; Endoplasmic Reticulum - metabolism; Humans; Inflammasomes - metabolism; inlfammasome; Interleukin-1beta - genetics; Interleukin-1beta - metabolism; interleukin-1β; Macrophages - metabolism; Macrophages - pathology; Male; Membrane Proteins - genetics; Membrane Proteins - metabolism; Mice; mitochondria; Mitochondria - metabolism; Mitochondria - pathology; mitochondrial-associated ER membrane; NLR Family, Pyrin Domain-Containing 3 Protein - genetics; NLR Family, Pyrin Domain-Containing 3 Protein - metabolism; ORMDL3; ulcerative colitis
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/j.jbc.2024.107120

Genome-wide association studies in inflammatory bowel disease have identified risk loci in the orosomucoid-like protein 3/ORMDL sphingolipid biosynthesis regulator 3 (ORMDL3) gene to confer susceptibility to ulcerative colitis (UC), but the underlying functional relevance remains unexplored. Here, we found that a subpopulation of the UC patients who had higher disease activity shows enhanced expression of ORMDL3 compared to the patients with lower disease activity and the non-UC controls. We also found that the patients showing high ORMDL3 mRNA expression have elevated interleukin-1β cytokine levels indicating positive correlation. Further, knockdown of ORMDL3 in the human monocyte-derived macrophages resulted in significantly reduced interleukin-1β release. Mechanistically, we report for the first time that ORMDL3 contributes to a mounting inflammatory response via modulating mitochondrial morphology and activation of the NLRP3 inflammasome. Specifically, we observed an increased fragmentation of mitochondria and enhanced contacts with the endoplasmic reticulum (ER) during ORMDL3 over-expression, enabling efficient NLRP3 inflammasome activation. We show that ORMDL3 that was previously known to be localized in the ER also becomes localized to mitochondria-associated membranes and mitochondria during inflammatory conditions. Additionally, ORMDL3 interacts with mitochondrial dynamic regulating protein Fis-1 present in the mitochondria-associated membrane. Accordingly, knockdown of ORMDL3 in a dextran sodium sulfate -induced colitis mouse model showed reduced colitis severity. Taken together, we have uncovered a functional role for ORMDL3 in mounting inflammation during UC pathogenesis by modulating ER-mitochondrial contact and dynamics.