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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在损伤外周神经中的差异时间表达。

Differential temporal 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 injured peripheral nerves.

作者信息

Ito Y, Yamamoto M, Li M, Doyu M, Tanaka F, Mutch T, Mitsuma T, Sobue G

机构信息

Department of Neurology, Nagoya University, School of Medicine, Nagoya 466-8550, Japan.

出版信息

Brain Res. 1998 May 18;793(1-2):321-7. doi: 10.1016/s0006-8993(98)00242-x.

Abstract

The mRNA expression of the neuropoietic cytokines, ciliary neurotrophic factor (CNTF), leukemia inhibitory factor (LIF), interleukin-6 (IL-6), and their receptor components (CNTFRalpha, LIFRbeta, IL-6Ralpha and gp130) was examined in peripheral nerves after two different types of injury, crush and transection. The CNTF mRNA expression levels decreased after injury and remained low in the transected model, but recovered in 4 weeks in the crushed model. The LIF mRNA rapidly increased after damage and returned gradually to control levels. The IL-6 mRNA expression increased rapidly within 1 day after injury but dramatically decreased soon after. The CNTFRalpha mRNA levels gradually increased after nerve injury. LIFRbeta was expressed in the intact nerve and decreased slightly after injury. The IL-6Ralpha expression was observed faintly in the intact nerve and increased significantly soon after injury. There was also an increase in the expression of gp130. Although the temporal expression of these neuropoietic cytokines and receptors was extremely different, their pattern was similar between the crushed and transected models, except for CNTF. These results suggest that the expression of the ligands and receptors are differentially regulated after peripheral nerve injury, implying that each cytokine and signal transduction system has entirely distinctive functions in neuronal regeneration and repair.

摘要

在挤压伤和横断伤这两种不同类型的损伤后,检测了周围神经中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)、白细胞介素-6(IL-6)及其受体成分(CNTFRα、LIFRβ、IL-6Rα和gp130)的mRNA表达。损伤后CNTF mRNA表达水平下降,在横断模型中持续较低水平,但在挤压模型中4周后恢复。LIF mRNA在损伤后迅速增加,并逐渐恢复到对照水平。IL-6 mRNA表达在损伤后1天内迅速增加,但随后很快大幅下降。神经损伤后CNTFRα mRNA水平逐渐升高。LIFRβ在完整神经中表达,损伤后略有下降。IL-6Rα在完整神经中表达微弱,损伤后很快显著增加。gp130的表达也增加。尽管这些神经生成细胞因子及其受体的时间表达差异极大,但除了CNTF外,它们在挤压模型和横断模型中的表达模式相似。这些结果表明,周围神经损伤后配体和受体的表达受到不同调节,这意味着每种细胞因子和信号转导系统在神经元再生和修复中具有完全不同的功能。

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