Commensal Bacteria-Dependent CD8αβ(+) T Cells in the Intestinal Epithelium Produce Antimicrobial Peptides

肠道上皮细胞中依赖于共生细菌的CD8αβ(+) T细胞产生抗菌肽

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Abstract

The epithelium of the intestine functions as the primary "frontline" physical barrier for protection from enteric microbiota. Intraepithelial lymphocytes (IELs) distributed along the intestinal epithelium are predominantly CD8(+) T cells, among which CD8αβ(+) IELs are a large population. In this investigation, the proportion and absolute number of CD8αβ(+) IELs decreased significantly in antibiotic-treated and germ-free mice. Moreover, the number of CD8αβ(+) IELs was correlated closely with the load of commensal microbes, and induced by specific members of commensal bacteria. Microarray analysis revealed that CD8αβ(+) IELs expressed a series of genes encoding potent antimicrobial peptides (AMPs), whereas CD8αβ(+) splenocytes did not. The antimicrobial activity of CD8αβ(+) IELs was confirmed by an antimicrobial-activity assay. In conclusion, microbicidal CD8αβ(+) IELs are regulated by commensal bacteria which, in turn, secrete AMPs that have a vital role in maintaining the homeostasis of the small intestine.

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