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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Lymph node stromal cells support dendritic cell-induced gut-homing of T cells.
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Lymph node stromal cells support dendritic cell-induced gut-homing of T cells.

机译:淋巴结基质细胞支持树突状细胞诱导的T细胞肠归巢。

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摘要

T cells are imprinted to express tissue-specific homing receptors upon activation in tissue-draining lymph nodes, resulting in their migration to the site of Ag entry. Expression of gut-homing molecules alpha(4)beta(7) and CCR9 is induced by retinoic acid, a vitamin A metabolite produced by retinal dehydrogenases, which are specifically expressed in dendritic cells as well as stromal cells in mucosa-draining lymph nodes. In this study, we demonstrate that mesenteric lymph node stromal cell-derived retinoic acid can directly induce the expression of gut-homing molecules on proliferating T cells, a process strongly enhanced by bone marrow-derived dendritic cells in vitro. Therefore, cooperation of sessile lymph node stromal cells with mobile dendritic cells warrants the imprinting of tissue specific homing receptors on activated T cells.
机译:T细胞在引流组织的淋巴结中被激活后被印记表达组织特异性的归巢受体,导致它们迁移到Ag进入位点。肠归巢分子α(4)beta(7)和CCR9的表达是由视黄酸诱导的,视黄酸是一种由视网膜脱氢酶产生的维生素A代谢产物,在黏膜引流​​的淋巴结中的树突状细胞和基质细胞中都有特异性表达。在这项研究中,我们证明了肠系膜淋巴结基质细胞衍生的视黄酸可以直接诱导增殖型T细胞上肠归巢分子的表达,这一过程在体外被骨髓衍生的树突状细胞强烈增强。因此,无柄淋巴结基质细胞与活动树突状细胞的协作保证了组织特异性归巢受体在活化的T细胞上的印记。

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