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睫状神经营养因子(CNTF)、白血病抑制因子(LIF)、白细胞介素-6(IL-6)及其受体(CNTFRα、LIFRβ、IL-6Rα和gp130)的mRNA在人类周围神经病变中的表达

Expression of mRNAs for ciliary neurotrophic factor (CNTF), leukemia inhibitory factor (LIF), interleukin-6 (IL-6), and their receptors (CNTFR alpha, LIFR beta, IL-6R alpha, and gp130) in human peripheral neuropathies.

作者信息

Ito Y, Yamamoto M, Mitsuma N, Li M, Hattori N, Sobue G

机构信息

Department of Neurology, Nagoya University School of Medicine, Japan.

出版信息

Neurochem Res. 2001 Jan;26(1):51-8. doi: 10.1023/a:1007628631985.

Abstract

The mRNA levels of neuropoietic cytokines, ciliary neurotrophic factor (CNTF), leukemia inhibitory factor (LIF), and interleukin-6 (IL-6), and their receptor components (CNTFR alpha, LIFR beta, IL-6R alpha, and gp130) were examined in seventy-six patients with various peripheral neuropathies to determine the extent of expression of these cytokines and receptors, and their relationship to nerve fiber pathology and cell infiltration in the diseased nerves. The CNTF mRNA levels were significantly decreased in the diseased nerves and were correlated to residual myelinated fiber population. In contrast, the mRNA levels of LIF, IL-6 and the ligand-binding receptor components (CNTFR alpha, LIFR beta and IL-6R alpha) were elevated to variable extent in the diseased nerves. The CNTFR alpha, LIFR beta, and IL-6R alpha mRNA levels showed a weak positive correlation with the extent of demyelinating pathology and their levels were related to each other. Moreover, the CNTF and LIF mRNA levels were inversely proportional to the extent of macrophage invasion, whereas the CNTFR alpha and IL-6R alpha mRNA expressions were correlated to the increase in macrophage infiltration. The neuropoietic cytokine family and its receptor expressions in the diseased human nerves are regulated by an underlying pathology-related process rather than type of diseases, and could play a role in peripheral nerve regeneration and repair.

摘要

在76例患有各种周围神经病变的患者中,检测了神经生成细胞因子、睫状神经营养因子(CNTF)、白血病抑制因子(LIF)和白细胞介素-6(IL-6)及其受体成分(CNTFRα、LIFRβ、IL-6Rα和gp130)的mRNA水平,以确定这些细胞因子和受体的表达程度,以及它们与患病神经中神经纤维病理和细胞浸润的关系。患病神经中CNTF mRNA水平显著降低,并与残留有髓纤维数量相关。相反,患病神经中LIF、IL-6以及配体结合受体成分(CNTFRα、LIFRβ和IL-6Rα)的mRNA水平在不同程度上升高。CNTFRα、LIFRβ和IL-6Rα mRNA水平与脱髓鞘病理程度呈弱正相关,且它们的水平相互关联。此外,CNTF和LIF mRNA水平与巨噬细胞浸润程度成反比,而CNTFRα和IL-6Rα mRNA表达与巨噬细胞浸润增加相关。患病人类神经中神经生成细胞因子家族及其受体表达受潜在病理相关过程而非疾病类型的调节,并可能在周围神经再生和修复中发挥作用。

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