MLKL deficiency inhibits DSS-induced colitis independent of intestinal microbiota.

Abstract:

:The maintenance of intestinal tissue homeostasis is vital for the resistance against inflammatory bowel diseases (IBDs). Necroptosis is identified as an alternative mode of regulated cell death, which plays a pivotal role in tissue homeostasis. Thus, the roles of RIP3-mediated necroptosis in intestinal inflammation have been extensively studied. However, the biological implications of the mixed lineage kinase-like protein (MLKL), a molecule downstream of RIP3 in gut remain unclear. In this study, the role of MLKL in DSS-induced colitis was examined, and the contribution of gut microbiota was also determined. Compared with non-littermate WT mice, the survival rate, clinical score, intestinal damage and intestinal mucosal barrier integrity of non-littermate MLKL-deficient mice are significantly improved. MLKL deficiency prevents inflammatory cytokines production and MAPK signaling activation. Hence, MLKL deficiency inhibits DSS-induced colitis. Moreover, we proved that DSS susceptibility difference between two genotypes is not driven by intestinal microbiota based on the co-housing of two non-littermate genotypes and qPCR detection of fecal dominant bacterial taxa.

journal_name

Mol Immunol

journal_title

Molecular immunology

authors

Zhang J,Qin D,Yang YJ,Hu GQ,Qin XX,Du CT,Chen W

doi

10.1016/j.molimm.2019.01.018

subject

Has Abstract

pub_date

2019-03-01 00:00:00

pages

132-141

eissn

0161-5890

issn

1872-9142

pii

S0161-5890(18)31043-5

journal_volume

107

pub_type

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