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CXCL14在健康人类和小鼠上皮组织中的组成性表达。

Constitutive expression of CXCL14 in healthy human and murine epithelial tissues.

作者信息

Meuter Simone, Moser Bernhard

机构信息

Institute of Cell Biology, University of Bern, Balzerstrasse 4, 3012 Bern, Switzerland.

出版信息

Cytokine. 2008 Nov;44(2):248-55. doi: 10.1016/j.cyto.2008.08.009. Epub 2008 Sep 21.

Abstract

CXCL14 (BRAK) is an ill-described chemokine with unknown receptor selectivity. The human chemokine is constitutively expressed in epithelial tissues and is selective for dendritic cell precursors, indicating a possible function in the maintenance of epithelial DCs. Several studies have addressed the question of human CXCL14 expression in cancerous tissues; however, distribution in healthy tissues and, in particular, the cellular origin of this chemokine has not been thoroughly investigated. The expression pattern of murine CXCL14 is largely unknown. In agreement with the human chemokine, we demonstrated ubiquitous and constitutive expression of murine CXCL14 in various tissues, foremost in those of epithelial origin such as the skin and the gastrointestinal tract. In addition, we did not find any CXCL14 in lymphoid tissues. Interestingly and in contrast to humans, murine CXCL14 was strongly expressed in the lung. In the skin, CXCL14 was produced by keratinocytes and dermal macrophages in both mice and humans, whereas CXCL14-expressing mast cells could only be found in the human dermis. Therefore, despite the remarkable structural homology and the broad similarity in the tissue distribution of human and murine CXCL14, distinct differences point to diverse, species-specific needs for CXCL14 in epithelial immunity.

摘要

CXCL14(BRAK)是一种描述较少的趋化因子,其受体选择性未知。这种人类趋化因子在上皮组织中组成性表达,对树突状细胞前体具有选择性,表明其在上皮树突状细胞维持中可能发挥作用。多项研究探讨了人类CXCL14在癌组织中的表达问题;然而,其在健康组织中的分布,尤其是这种趋化因子的细胞来源尚未得到充分研究。小鼠CXCL14的表达模式在很大程度上尚不清楚。与人类趋化因子一致,我们证明小鼠CXCL14在各种组织中普遍且组成性表达,最主要是在那些上皮来源的组织中,如皮肤和胃肠道。此外,我们在淋巴组织中未发现任何CXCL14。有趣的是,与人类不同,小鼠CXCL14在肺中强烈表达。在皮肤中,小鼠和人类的角质形成细胞及真皮巨噬细胞均可产生CXCL14,而表达CXCL14的肥大细胞仅在人类真皮中发现。因此,尽管人类和小鼠CXCL14在结构上具有显著同源性且在组织分布上具有广泛相似性,但明显的差异表明在上皮免疫中对CXCL14存在不同的物种特异性需求。

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