Division of Immune Regulation, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.
J Immunol. 2012 Sep 15;189(6):2697-701. doi: 10.4049/jimmunol.1201248. Epub 2012 Aug 15.
Dendritic cells (DC) in the gut promote immune tolerance by expressing retinal dehydrogenase (RALDH), an enzyme that promotes retinoic acid, which aids differentiation of Foxp3+ inducible regulatory T cells (iTreg) in the intestinal mucosa. How RALDH expression is regulated is unclear. We found that 4-1BB (CD137), a member of the TNFR family, together with CD103, marked mesenteric lymph node DC with the highest level of RALDH activity, and ligation of 4-1BB maintained RALDH expression in these gut DC. Moreover, 4-1BB signals synergized with those through TLR2 or GM-CSFR to promote RALDH activity in undifferentiated DC. Correspondingly, 4-1BB-deficient mice were impaired in their ability to generate iTreg in the GALT when exposed to oral Ag, and 4-1BB-deficient mesenteric lymph node DC displayed weak RALDH activity and were poor at promoting iTreg development. Thus, our data demonstrate a novel activity of 4-1BB in controlling RALDH expression and the regulatory activity of DC.
肠道树突状细胞 (DC) 通过表达视黄醛脱氢酶 (RALDH) 促进免疫耐受,RALDH 是一种促进肠道黏膜中 Foxp3+诱导性调节性 T 细胞 (iTreg) 分化的酶。RALDH 表达的调控机制尚不清楚。我们发现 4-1BB(CD137),一种 TNFR 家族成员,与 CD103 一起标记肠系膜淋巴结 DC 中具有最高 RALDH 活性的细胞,4-1BB 的交联可维持这些肠道 DC 中的 RALDH 表达。此外,4-1BB 信号与 TLR2 或 GM-CSFR 信号协同作用,促进未分化 DC 中 RALDH 活性。相应地,在口服 Ag 暴露时,4-1BB 缺陷小鼠在 GALT 中生成 iTreg 的能力受损,而 4-1BB 缺陷肠系膜淋巴结 DC 显示出较弱的 RALDH 活性,并且在促进 iTreg 发育方面能力较差。因此,我们的数据表明 4-1BB 在控制 RALDH 表达和 DC 调节活性方面具有新的作用。