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外周神经损伤后睫状神经营养因子的时空表达

Temporal and spatial expression of ciliary neurotrophic factor after peripheral nerve injury.

作者信息

Smith G M, Rabinovsky E D, McManaman J L, Shine H D

机构信息

Department of Neurosurgery, Baylor College of Medicine, Houston, Texas 77030.

出版信息

Exp Neurol. 1993 Jun;121(2):239-47. doi: 10.1006/exnr.1993.1091.

Abstract

Schwann cells in the intact sciatic nerve express high amounts of ciliary neurotrophic factor (CNTF), but 7 days after injury to the nerve expression dramatically decreases. To determine whether this change occurs only in the region of the injury or throughout the whole nerve we examined the spatial and temporal expression of CNTF after a crush injury. One day after injury the amount of CNTF mRNA and protein decreased within the first 4 mm distal to the crush site. This decrease progressed in a centrifugal manner distally until mRNA and protein were scarcely detectable by 7 days. In nerve proximal to the crush site CNTF expression decreased slightly and was still detectable at all sample times. During regeneration CNTF expression remained very low up to 14 days after injury. By 30 days mRNA and protein were detectable and by 60 days CNTF protein was present at normal amounts. Immunohistochemical analysis of normal nerve revealed CNTF localized in outer portion of the cytoplasm of myelin-forming Schwann cells. Three days after injury CNTF coalesced with pockets of cytoplasm in the Schwann cell and by 5 days was barely detectable. Positive staining remained in proximal segments where little or no degeneration occurred. These results demonstrate that CNTF expression in Schwann cells is synchronized with their functional state. CNTF expression decreases with demyelination during Wallerian degeneration and returns to normal following remyelination during regeneration. These findings also suggest that CNTF expression requires intact axon-Schwann cell interactions.

摘要

完整坐骨神经中的施万细胞表达大量睫状神经营养因子(CNTF),但在神经损伤7天后,其表达显著下降。为了确定这种变化是仅发生在损伤区域还是整个神经中,我们检查了挤压伤后CNTF的时空表达。损伤后一天,挤压部位远端前4毫米内CNTF mRNA和蛋白质的量减少。这种减少以离心方式向远端进展,直到7天时mRNA和蛋白质几乎检测不到。在挤压部位近端的神经中,CNTF表达略有下降,在所有采样时间仍可检测到。在再生过程中,直到损伤后14天CNTF表达一直很低。到30天时可检测到mRNA和蛋白质,到60天时CNTF蛋白质含量恢复正常。正常神经的免疫组织化学分析显示CNTF定位于形成髓鞘的施万细胞胞质的外部。损伤后三天,CNTF与施万细胞中的细胞质小泡合并,到5天时几乎检测不到。在几乎没有或没有发生变性的近端节段中仍保留阳性染色。这些结果表明,施万细胞中CNTF的表达与其功能状态同步。在沃勒变性期间,随着脱髓鞘CNTF表达下降,在再生期间髓鞘再生后恢复正常。这些发现还表明,CNTF的表达需要完整的轴突 - 施万细胞相互作用。

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