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慢性炎性脱髓鞘性多发性神经病(CIDP)腓肠神经活检中肿瘤坏死因子α(TNF alpha)、干扰素γ(IFN gamma)和白细胞介素-2(IL-2)mRNA的表达

TNF alpha, IFN gamma and IL-2 mRNA expression in CIDP sural nerve biopsies.

作者信息

Mathey E K, Pollard J D, Armati P J

机构信息

School of Biological Sciences, University of Sydney, NSW, Australia.

出版信息

J Neurol Sci. 1999 Feb 1;163(1):47-52. doi: 10.1016/s0022-510x(99)00009-x.

Abstract

Proinflammatory cytokines contribute to the regulation of the disease process in inflammatory neuropathies. Cellular localisation of cytokine expression in CIDP nerve biopsies should provide further insight into the pathogenic mechanisms of the disease and the individual cells involved. In this study in situ hybridisation was used to determine the exact localisation and identity of cells that express TNF alpha, IFN gamma and IL-2 mRNA within the CIDP nerve. Paraffin embedded and frozen sural nerve biopsies from three acute phase CIDP patients were used for the study. Sections of these samples were probed with digoxigenin labelled oligoprobes for TNF alpha, IFN gamma and IL-2. The results demonstrate localisation of cytokine expression to the inner rim of the perineurium, epineurial and endoneurial blood vessels and infiltrating inflammatory cells. In addition strong staining for TNF alpha. mRNA was widespread in the endoneurium in areas consistent with/suggestive of Schwann cells. Expression of cytokines in the perineurium and endoneurial blood vessels may have pertinent implications with respect to the breakdown of the blood nerve barrier associated with CIDP. In the very least the potential for an immunomodulatory role may be ascribed to these cells.

摘要

促炎细胞因子有助于调节炎性神经病的疾病进程。慢性炎症性脱髓鞘性多发性神经病(CIDP)神经活检中细胞因子表达的细胞定位应能进一步深入了解该疾病的致病机制以及所涉及的单个细胞。在本研究中,原位杂交用于确定CIDP神经内表达肿瘤坏死因子α(TNFα)、干扰素γ(IFNγ)和白细胞介素-2(IL-2)mRNA的细胞的确切定位和特性。使用了来自三名急性期CIDP患者的石蜡包埋和冷冻腓肠神经活检样本进行研究。这些样本的切片用洋地黄毒苷标记的寡核苷酸探针检测TNFα、IFNγ和IL-2。结果表明细胞因子表达定位于神经束膜的内缘、神经外膜和神经内膜血管以及浸润的炎性细胞。此外,TNFα mRNA的强染色在神经内膜中广泛存在于与施万细胞一致/提示施万细胞的区域。神经束膜和神经内膜血管中细胞因子的表达可能与CIDP相关的血神经屏障破坏有密切关系。至少可以将免疫调节作用的潜力归因于这些细胞。

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