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在皮质脊髓束轴突生长和靶神经支配过程中,大鼠脊髓中N - 细胞黏附分子(N-CAM)表位的发育性表达。

Developmental expression of N-CAM epitopes in the rat spinal cord during corticospinal tract axon outgrowth and target innervation.

作者信息

Joosten E A

机构信息

Department of Anatomy and Cell Biology, Georgetown University Medical School, Washington, DC 20007.

出版信息

Brain Res Dev Brain Res. 1994 Apr 15;78(2):226-36. doi: 10.1016/0165-3806(94)90030-2.

Abstract

The neural cell adhesion molecule (N-CAM) is an integral membrane glycoprotein which mediates the adhesion of neurons to neurons and to other types of cells. During development, the N-CAM molecule is converted from a microheterogenous, highly sialylated, embryonic form (200-230 kDa) to several distinct, less sialylated but more adhesive, adult forms (120, 140 and 180 kDa). Monoclonal antibodies to epitopes of N-CAM (designated 5A5, 12F8, 5B8, 12F11 and 14E6) were used to investigate the spatial and temporal distribution of these neural cell adhesion molecules during the development of the corticospinal tract (CST) in rat spinal cord, from postnatal day 1 (P1) until adulthood. The light microscopical observations indicate that the embryonic form of N-CAM (200-230 kDa) recognized by 5A5 and 12F8 antibodies, respectively, is probably involved in the process of initial ingrowth of pioneer CST-fibers into the ventralmost part of the dorsal funiculus. The adult forms of N-CAM (120, 140, 180 kDa) recognized by 5B8, 12F11, and 14E6 antibodies, respectively, are present during later stages of CST white matter ingrowth and probably involved in fasciculation of the later arriving CST axons. During the period of CST target innervation (P4-P21), a gradual shift from embryonic (200-230 kDa) to adult (120, 140 and 180 kDa) forms of N-CAM occurs in spinal white matter and in the spinal gray matter adjacent to the ventral most part of the dorsal funiculus. The presence of embryonic N-CAM (200 kDa), with its low adhesive capacity in the CST outgrowth area may allow the CST axons to branch. If this branching is no longer desirable, only the higher affinity forms of N-CAM (120, 140 and 180 kDa) are expressed. The absence of N-CAM on CST target interneurons in the base of the dorsal horn and intermediate spinal gray matter strongly suggest that N-CAM is not involved in CST synapse formation. Together, these results suggest that various forms of N-CAM are involved in CST spinal white matter tract formation and subsequent target innervation, but not in the process of synapse formation.

摘要

神经细胞黏附分子(N-CAM)是一种整合膜糖蛋白,它介导神经元与神经元以及与其他类型细胞的黏附。在发育过程中,N-CAM分子从一种微异质性、高度唾液酸化的胚胎形式(200 - 230 kDa)转变为几种不同的、唾液酸化程度较低但黏附性更强的成年形式(120、140和180 kDa)。针对N-CAM表位的单克隆抗体(命名为5A5、12F8、5B8、12F11和14E6)被用于研究大鼠脊髓皮质脊髓束(CST)从出生后第1天(P1)到成年期发育过程中这些神经细胞黏附分子的空间和时间分布。光学显微镜观察表明,分别被5A5和12F8抗体识别的N-CAM胚胎形式(200 - 230 kDa)可能参与了先驱CST纤维最初向内生长至背索最腹侧部分的过程。分别被5B8、12F11和14E6抗体识别的N-CAM成年形式(120、140、180 kDa)在CST白质向内生长的后期阶段出现,可能参与了后来到达的CST轴突的成束过程。在CST靶标神经支配期(P4 - P21),脊髓白质和与背索最腹侧部分相邻的脊髓灰质中,N-CAM从胚胎形式(200 - 230 kDa)向成年形式(120、140和180 kDa)逐渐转变。胚胎型N-CAM(200 kDa)在CST生长区域黏附能力较低,这可能使CST轴突能够分支。如果这种分支不再需要,就只表达亲和力更高的N-CAM形式(120、140和180 kDa)。背角基部和脊髓中间灰质中CST靶标中间神经元上不存在N-CAM,这强烈表明N-CAM不参与CST突触的形成。总之,这些结果表明,各种形式的N-CAM参与了CST脊髓白质束的形成及随后的靶标神经支配,但不参与突触形成过程。

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