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首页> 外文期刊>Biotechnic and Histochemistry >The chemokine, CXCL16, and its receptor, CXCR6, are constitutively expressed in human annulus fibrosus and expression of CXCL16 is up-regulated by exposure to IL-1 ss in vitro
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The chemokine, CXCL16, and its receptor, CXCR6, are constitutively expressed in human annulus fibrosus and expression of CXCL16 is up-regulated by exposure to IL-1 ss in vitro

机译:趋化因子,CXCL16及其受体CXCR6在人环纤维体中组成型表达,并通过暴露于体外暴露于IL-1 SS的CXCL16的表达

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摘要

Chemokines are an important group of soluble molecules with specialized functions in inflammation. The roles of many specialized chemokines and their receptors remain poorly understood in the human intervertebral disc. We investigated CXCL16 and its receptor, CXCR6, to determine their immunolocalization in disc tissue and their presence following exposure of cultured human annulus fibrosus cells to proinflammatory cytokines. CXCL16 is a marker for inflammation; it also can induce hypoxia-inducible factor 1 alpha (HIF-1 alpha), which is a phenotypic marker of heathy nucleus pulposus tissue. We found CXCL16 and CXCR6 immunostaining in many cells of the annulus portion of the disc. Molecular studies showed that annulus fibrosus cells exposed to IL-1 ss, but not TNF-alpha, exhibited significant up-regulation of CXCL16 expression vs. control cells. There was no significant difference in the percentage of annulus cells that exhibited immunolocalization of CXCL16 in grade I/II, grade III or grade IV/V specimens. The presence of CXCL16 and its receptor, CXCR6, in the annulus in vivo suggests the need for future research concerning the role of this chemokine in proinflammatory functions, HIF-1 alpha expression and disc vascularization.
机译:趋化因子是一种重要的溶解分子,具有炎症的专门功能。许多专用趋化因子及其受体的角色在人椎间盘中仍然明白很差。我们研究了CXCL16及其受体CXCR6,以确定其在椎间盘组织中的免疫橡胶化及其在暴露于培养的人环纤维细胞中以促进炎症细胞因子。 CXCL16是炎症的标志物;它还可以诱导缺氧 - 诱导因子1α(HIF-1α),其是异质髓核组织的表型标志物。我们发现CXCL16和CXCR6免疫染色盘的环形部分的许多细胞中。分子研究表明,暴露于IL-1SS但不是TNF-α的环形纤维细胞表现出CXCl16表达与对照细胞的显着上调。在I / II级,III级或IV级/级标本中表现出CXCL16免疫循环化的环形细胞百分比没有显着差异。 CXCL16及其受体CXCR6在Vivo中的存在表明,需要对未来的研究有关该趋化因子在促炎功能中的作用,HIF-1α表达和盘血管化。

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