| Literature DB >> 33894128 |
Changsheng Xing1, Mingjun Wang2, Adebusola A Ajibade2, Peng Tan3, Chuntang Fu4, Lang Chen5, Motao Zhu1, Zhao-Zhe Hao6, Junjun Chu1, Xiao Yu2, Bingnan Yin1, Jiahui Zhu7, Wan-Jou Shen8, Tianhao Duan1, Helen Y Wang9, Rong-Fu Wang10.
Abstract
Microbiota play critical roles in regulating colitis and colorectal cancer (CRC). However, it is unclear how the microbiota generate protective immunity against these disease states. Here, we find that loss of the innate and adaptive immune signaling molecule, TAK1, in myeloid cells (Tak1ΔM/ΔM) yields complete resistance to chemical-induced colitis and CRC through microbiome alterations that drive protective immunity. Tak1ΔM/ΔM mice exhibit altered microbiota that are critical for resistance, with antibiotic-mediated disruption ablating protection and Tak1ΔM/ΔM microbiota transfer conferring protection against colitis or CRC. The altered microbiota of Tak1ΔM/ΔM mice promote IL-1β and IL-6 signaling pathways, which are required for induction of protective intestinal Th17 cells and resistance. Specifically, Odoribacter splanchnicus is abundant in Tak1ΔM/ΔM mice and sufficient to induce intestinal Th17 cell development and confer resistance against colitis and CRC in wild-type mice. These findings identify specific microbiota strains and immune mechanisms that protect against colitis and CRC.Entities:
Keywords: Bacteroides sp. D20; Odoribacter splanchnicus; TAK1 signaling; Th17 cells; acute colitis; colon cancer; innate immunity; microbiota
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Year: 2021 PMID: 33894128 PMCID: PMC8192480 DOI: 10.1016/j.chom.2021.03.016
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 31.316