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首页> 外文期刊>Developmental Immunology: Journal of Immunology Research >In Vivo and In VitroExpression of Tenascin by HumanThymic Microenvironmental Cells
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In Vivo and In VitroExpression of Tenascin by HumanThymic Microenvironmental Cells

机译:人胸腺微环境细胞体内腱生蛋白的体外表达

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Increasing evidence reveals that extracellular matrix components can be regarded as a groupof mediators in intrathymic T-cell migration and/or differentiation. Yet, little is kown aboutthe expression and putative function of one particular extracellular matrix protein, namely,tenascin in the thymus. Herein we investigated, by means of immunocytochemistry,tenascin expression in normal infant and fetal human thymuses, as well as in cultures ofthymic microenvironmental cells.In situ, tenascin distribution is restricted to the medulla and cortico-medullary regions ofnormal thymuses. This pattern thus differed from that of fibronectin, laminin and type IVcollagen, in which subseptal basement membranes were strongly labeled. Interestingly,tenascin did not co-localize with the cytokeratin-defined thymic epithelial cell network. Thiswas in keeping with thein vitrodata showing that tenascin-bearing cells were nonepithelial(and probably nonfibroblastic) microenvironmental elements.Studies with fetal thymuses revealed a developmentally regulated expression of tenascin,with a faint but consistent network labeling, in thymic rudiments as early as 12 weeks ofgestational age, that progressed to a strong TN expression at 18 weeks of fetal development,which was similar to the distribution pattern observed thereafter, including postnatally.Our results clearly indicated that tenascin is constitutively expressed in the humanthymus, since early stages of thymic ontogeny, and suggest that the cell type responsible forits secretion is a nonepithelial microenvironmental cell.
机译:越来越多的证据表明,细胞外基质成分可被视为胸腺内T细胞迁移和/或分化的一组介体。然而,人们对一种特殊的细胞外基质蛋白,即胸腺中的腱生蛋白的表达和推测功能知之甚少。本文中,我们通过免疫细胞化学研究了肌腱蛋白在正常婴儿和胎儿人类胸腺以及胸腺微环境细胞培养物中的表达。肌腱蛋白的分布仅限于正常胸腺的髓质和皮质-髓质区域。因此,这种模式不同于纤连蛋白,层粘连蛋白和IV型胶原蛋白,在这些类型中,隔壁基底膜被强烈标记。有趣的是,肌腱蛋白未与细胞角蛋白定义的胸腺上皮细胞网络共定位。这与体外数据表明载有肌腱蛋白的细胞是非上皮的(可能是非成纤维细胞的)微环境元素相一致的。胎儿胸腺的研究表明,早在第12周,在胸腺瘤中,肌腱蛋白的表达受发育调控,具有淡淡但一致的网络标记。胎龄,在胎儿发育的18周时发展到一个强TN表达,这与此后(包括出生后)观察到的分布模式相似。我们的结果清楚地表明,自胸腺发育的早期阶段,肌腱蛋白在人胸腺中组成性表达,并提示负责其分泌的细胞类型是非上皮微环境细胞。

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