Martini R, Schachner M
Department of Neurobiology, University of Heidelberg, Federal Republic of Germany.
J Cell Biol. 1988 May;106(5):1735-46. doi: 10.1083/jcb.106.5.1735.
The localization of the neural cell adhesion molecules L1, N-CAM, and the myelin-associated glycoprotein was studied by pre- and postembedding staining procedures at the light and electron microscopic levels in transected and crushed adult mouse sciatic nerve. During the first 2-6 d after transection, myelinated and nonmyelinated axons degenerated in the distal part of the proximal stump close to the transection site and over the entire length of the distal part of the transected nerve. During this time, regrowing axons were seen only in the proximal, but not in the distal nerve stump. In most cases L1 and N-CAM remained detectable at cell contacts between nonmyelinating Schwann cells and degenerating axons as long as these were still morphologically intact. Similarly, myelin-associated glycoprotein remained detectable in the periaxonal area of the degenerating myelinated axons. During and after degeneration of axons, nonmyelinating Schwann cells formed slender processes which were L1 and N-CAM positive. They resembled small-diameter axons but could be unequivocally identified as Schwann cells by chronical denervation. Unlike the nonmyelinating Schwann cells, only few myelinating ones expressed L1 and N-CAM. At the cut ends of the nerve stumps a cap developed (more at the proximal than at the distal stump) that contained S-100-negative and fibronectin-positive fibroblast-like cells. Most of these cells were N-CAM positive but always L1 negative. Growth cones and regrowing axons expressed N-CAM and L1 at contact sites with these cells. Regrowing axons of small diameter were L1 and N-CAM positive where they made contact with each other or with Schwann cells, while large-diameter axons were only poorly antigen positive or completely negative. 14 d after transection, when regrowing axons were seen in the distal part of the transected nerve, regrowing axons made L1- and N-CAM-positive contacts with Schwann cells. When contacting basement membrane, axons were rarely found to express L1 and N-CAM. Most, if not all, Schwann cells associated with degenerating myelin expressed L1 and N-CAM. In crushed nerves, the immunostaining pattern was essentially the same as in the cut nerve. During formation of myelin, the sequence of adhesion molecule expression was the same as during development: L1 disappeared and N-CAM was reduced on myelinating Schwann cells and axons after the Schwann cell process had turned approximately 1.5 loops around the axon. Myelin-associated glycoprotein then appeared both periaxonally and on the turning loops of Schwann cells in the uncompacted myelin.(ABSTRACT TRUNCATED AT 400 WORDS)
通过包埋前和包埋后染色程序,在光镜和电镜水平上研究了成年小鼠坐骨神经横断和挤压后神经细胞粘附分子L1、N-CAM和髓磷脂相关糖蛋白的定位。在横断后的最初2-6天内,有髓和无髓轴突在近端残端靠近横断部位的远端部分以及横断神经远端部分的全长范围内发生退变。在此期间,仅在近端神经残端而非远端神经残端可见再生轴突。在大多数情况下,只要非髓鞘雪旺细胞与退变轴突之间的细胞接触在形态上仍保持完整,L1和N-CAM就仍可检测到。同样,在退变有髓轴突的轴周区域仍可检测到髓磷脂相关糖蛋白。在轴突退变期间及之后,非髓鞘雪旺细胞形成细长的突起,这些突起L1和N-CAM呈阳性。它们类似于小直径轴突,但通过长期去神经支配可明确鉴定为雪旺细胞。与非髓鞘雪旺细胞不同,只有少数髓鞘形成雪旺细胞表达L1和N-CAM。在神经残端的切断端形成了一个帽(近端比远端残端更多),其中包含S-100阴性和纤连蛋白阳性的成纤维细胞样细胞。这些细胞大多数N-CAM呈阳性,但L1始终呈阴性。生长锥和再生轴突在与这些细胞的接触部位表达N-CAM和L1。小直径的再生轴突在相互接触或与雪旺细胞接触处L1和N-CAM呈阳性,而大直径轴突抗原阳性较弱或完全阴性。横断后14天,当在横断神经的远端部分看到再生轴突时,再生轴突与雪旺细胞形成L1和N-CAM阳性接触。当与基底膜接触时,很少发现轴突表达L1和N-CAM。大多数(如果不是全部)与退变髓磷脂相关的雪旺细胞表达L1和N-CAM。在挤压的神经中,免疫染色模式与切断的神经基本相同。在髓磷脂形成过程中,粘附分子表达的顺序与发育过程中相同:在雪旺细胞突起围绕轴突转了约1.5圈后,L1在髓鞘形成雪旺细胞和轴突上消失,N-CAM减少。然后髓磷脂相关糖蛋白在未压实髓磷脂的轴周区域和雪旺细胞的转折环上均出现。(摘要截断于400字)