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白血病抑制因子由成年大鼠感觉神经元的一个独特群体逆向转运:与trkA及其他神经化学标志物共定位。

Leukaemia inhibitory factor is retrogradely transported by a distinct population of adult rat sensory neurons: co-localization with trkA and other neurochemical markers.

作者信息

Thompson S W, Vernallis A B, Heath J K, Priestley J V

机构信息

Division of Physiology, United Medical and Dental Schools, St Thomas' Hospital Medical School, London, UK.

出版信息

Eur J Neurosci. 1997 Jun;9(6):1244-51. doi: 10.1111/j.1460-9568.1997.tb01479.x.

Abstract

Sciatic sensory afferents that retrogradely transport and accumulate leukaemia inhibitory factor (LIF) within their soma were characterized in the adult rat in vivo. Twenty-four percent of neurons within the L4 and L5 dorsal root ganglia accumulated biotinylated LIF following intraneural injection of the cytokine into the sciatic nerve. Labelled cell bodies were predominantly of small diameter (20.1 +/- 0.5 microm). Retrograde transport was eliminated by excess unlabelled LIF but not by the related cytokines, ciliary-derived neurotrophic factor (CNTF) and interleukin-6 (IL-6). Double labelling revealed that the majority (81%) of LIF-accumulating neurons were immunopositive for CGRP and 34% were immunopositive for the cell surface glycoconjugate IB4. Sixty-two percent of LIF-accumulating neurons were immunopositive for trkA. Our results demonstrate a group of small-diameter sensory neurons that retrogradely transport LIF, comprising cells that constitutively express neuropeptides and those likely to be peptide-deficient. LIF-accumulating neurons expressing trkA are also potentially responsive to nerve growth factor. It is likely that the LIF-accumulating neurons described in this study are nociceptive in function.

摘要

在成年大鼠体内对坐骨神经感觉传入纤维进行了表征,这些纤维能在其胞体内逆行转运并积累白血病抑制因子(LIF)。将细胞因子注射到坐骨神经内后,L4和L5背根神经节内24%的神经元积累了生物素化的LIF。标记的细胞体主要直径较小(20.1±0.5微米)。过量未标记的LIF可消除逆行转运,但相关细胞因子睫状神经营养因子(CNTF)和白细胞介素-6(IL-6)则不能。双重标记显示,大多数(81%)积累LIF的神经元对降钙素基因相关肽(CGRP)免疫阳性,34%对细胞表面糖缀合物IB4免疫阳性。62%积累LIF的神经元对trkA免疫阳性。我们的结果表明,有一组小直径感觉神经元能逆行转运LIF,包括组成性表达神经肽的细胞和可能缺乏肽的细胞。表达trkA的积累LIF的神经元也可能对神经生长因子有反应。本研究中描述的积累LIF的神经元很可能具有伤害感受功能。

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