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在有和没有晶状体损伤的情况下,视神经挤压后大鼠视神经中排斥性导向分子 A 和新生蛋白的不同时空蛋白表达。

Different spatial and temporal protein expressions of repulsive guidance molecule a and neogenin in the rat optic nerve after optic nerve crush with and without lens injury.

机构信息

Centre for Ophthalmology, University Eye Hospital, Tübingen, Germany.

出版信息

J Neurosci Res. 2011 Apr;89(4):490-505. doi: 10.1002/jnr.22584. Epub 2011 Feb 2.

DOI:10.1002/jnr.22584
PMID:21290411
Abstract

The failure of lesioned mammalian CNS neurons to regenerate their axons remains a challenge. Evidence is emerging that repulsive proteins contribute to this failure. The repulsive guidance molecule A (RGMA) induces growth cone collapse in vitro, accumulates in the scar after spinal cord injury, and is up-regulated in glaucoma. In this study, we evaluated the spatial and temporal localization pattern of RGMA and its receptor neogenin in the optic nerve after optic nerve crush (ONC) without or with lens injury (LI) at up to nine time points (6 hr to 20 days) postsurgery by performing immunohistochemistry and Western blots. We found RGMA at the crush site (CS) and in the developing scar of ONC rats at every time point investigated, whereas it was absent in the CS of ONC + LI rats. Independent of the model, many cells were RGMA(+) in the ON: nerve fibers, blood vessels, astrocytes, oligodendrocytes, some microglia, some macrophages, and the sheath of the ON. Western blots showed a significantly lowered amount of RGMA in ONC + LI animals at 2, 4, and 6 days after crush compared with ONC animals. Furthermore, LI in sham-operated animals showed an increase of RGMA in six of eight time points compared with the sham-operated animals. Moreover, the effects of LI on the morphology of the ON were characterized at a level of detail never reported before. Our results show that RGMA is present and might contribute to the inhibitory environment in the ON, especially in and around the CS after ONC.

摘要

哺乳动物中枢神经系统损伤神经元的轴突再生失败仍然是一个挑战。有证据表明,排斥蛋白对此失败有一定的贡献。排斥导向分子 A(RGMA)在体外诱导生长锥塌陷,在脊髓损伤后积聚在疤痕中,并在青光眼患者中上调。在这项研究中,我们通过免疫组织化学和 Western blot 分析,评估了 RGMA 及其受体 neogenin 在视神经挤压(ONC)后没有或有晶状体损伤(LI)的情况下,在多达 9 个时间点(术后 6 小时至 20 天)在视神经中的空间和时间定位模式。我们发现,在每个研究时间点的视神经挤压大鼠的挤压部位(CS)和正在形成的疤痕中均存在 RGMA,而在视神经挤压+晶状体损伤大鼠的 CS 中则不存在。无论模型如何,在视神经中,许多细胞都是 RGMA(+):神经纤维、血管、星形胶质细胞、少突胶质细胞、一些小胶质细胞、一些巨噬细胞和视神经鞘。Western blot 显示,与视神经挤压大鼠相比,视神经挤压+晶状体损伤大鼠在挤压后 2、4 和 6 天的 RGMA 含量明显降低。此外,在假手术动物中,晶状体损伤在 8 个时间点中的 6 个时间点显示出 RGMA 增加,而在假手术动物中则没有。此外,晶状体损伤对视神经形态的影响在以前从未报道过的细节水平上进行了描述。我们的研究结果表明,RGMA 存在于视神经中,可能有助于抑制视神经中的抑制环境,尤其是在视神经挤压后 CS 内及其周围。

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