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RetinoicAcid Production by Intestinal Dendritic Cells

机译:肠道树突状细胞产生视黄酸

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摘要

Subpopulations of dendritic cells (DCs) in the small intestine and its related lymphoid organs can produce retinoic acid (RA) from vitamin A (retinol). Through the RA production, these DCs play a pivotal role in imprinting lymphocytes with gut-homing specificity, and contribute to the development of immune tolerance by enhancing the differentiation of Foxp3~+ regulatory T cells and inhibiting that of inflammatory Th17 cells. The RA-producing capacity in these DCs mostly depends on the expression of retinal dehydrogenase 2 (RALDH2, ALDH1A2). It is likely that the RALDH2 expression is induced in DCs by the microenvironmental factors in the small intestine and its related lymphoid organs. The major factor responsible for the RALDH2 expression appears to be GM-CSF. RA itself is essential for the GM-CSF-induced RALDH2 expression. IL-4 and IL-13 also enhance RALDH2 expression, but are dispensable. Toll-like receptor-mediated signals can also enhance the GM-CSF-induced RALDH2 expression in immature DCs.
机译:小肠中树突状细胞(DC)的亚群及其相关的淋巴器官可以从维生素A(视黄醇)中产生视黄酸(RA)。这些DC通过产生RA发挥关键作用,以肠道归巢特异性标记淋巴细胞,并通过增强Foxp3〜+调节性T细胞的分化并抑制炎性Th17细胞的分化而促进免疫耐受的发展。这些DC中产生RA的能力主要取决于视网膜脱氢酶2(RALDH2,ALDH1A2)的表达。可能由小肠及其相关淋巴器官的微环境因素在DC中诱导RALDH2表达。负责RALDH2表达的主要因素似乎是GM-CSF。 RA本身对于GM-CSF诱导的RALDH2表达至关重要。 IL-4和IL-13也可增强RALDH2表达,但不是必需的。 Toll样受体介导的信号还可以增强未成熟DC中GM-CSF诱导的RALDH2表达。

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