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连接蛋白和腱生蛋白对体外生长锥行为的影响。

Influence of janusin and tenascin on growth cone behavior in vitro.

作者信息

Taylor J, Pesheva P, Schachner M

机构信息

Department of Neurobiology, Swiss Federal Institute of Technology, Hönggerberg, Zurich.

出版信息

J Neurosci Res. 1993 Jul 1;35(4):347-62. doi: 10.1002/jnr.490350402.

Abstract

Janusin and tenascin are glia-derived, structurally related, extracellular matrix glycoproteins of the J1 family that are expressed in vivo at times and in locations where active neurite outgrowth occurs, but also when the formation or stabilization of cytoarchitectonic boundaries appears to be in operation. To resolve this apparent functional dichotomy, we have studied the behavioral response of growth cones, growing in culture on the permissive substrate laminin to janusin and tenascin, by video time lapse microscopy. When janusin and tenascin were offered as sharp substrate boundaries, dorsal root ganglion (DRG) and retinal ganglion neuron growth cones avoided growing on these molecules, but were not induced to collapse. On the other hand, when janusin and tenascin were offered, in a mixture with laminin, as uniform substrates, DRG growth cones displayed a collapsed morphology and were able to advance at a faster rate than on laminin alone. In contrast, the outgrowth of retinal ganglion neuron growth cones was completely inhibited under these conditions, underscoring a cell type specificity in the response of growth cones to these molecules. Using several monoclonal antibodies binding to distinct epitopes on the tenascin molecule, we have identified two domains responsible for growth cone repulsion, on epidermal growth factor (EGF)-like repeats 3-5 and fibronectin type III homologous repeats 4 and 5. These domains are different from the one previously recognized to be involved in neurite outgrowth on a uniform tenascin substrate. We conclude that both molecules may promote or retard growth cone advance, depending on the spatial expression pattern and the neuronal cell type.

摘要

腱生蛋白和腱糖蛋白是神经胶质细胞衍生的、结构相关的J1家族细胞外基质糖蛋白,在体内活跃的神经突生长发生时、以及细胞构筑边界的形成或稳定似乎正在进行时的特定时间和位置表达。为了解决这种明显的功能二分法,我们通过视频延时显微镜研究了在允许性底物层粘连蛋白上培养的生长锥对腱生蛋白和腱糖蛋白的行为反应。当腱生蛋白和腱糖蛋白作为清晰的底物边界提供时,背根神经节(DRG)和视网膜神经节神经元生长锥会避开在这些分子上生长,但不会被诱导塌陷。另一方面,当腱生蛋白和腱糖蛋白与层粘连蛋白混合作为均匀底物提供时,DRG生长锥呈现出塌陷的形态,并且能够比单独在层粘连蛋白上以更快的速度前进。相比之下,在这些条件下视网膜神经节神经元生长锥的生长完全受到抑制,这突出了生长锥对这些分子反应中的细胞类型特异性。使用几种结合腱糖蛋白分子上不同表位的单克隆抗体,我们在表皮生长因子(EGF)样重复序列3 - 5以及纤连蛋白III型同源重复序列4和5上鉴定出了两个负责生长锥排斥的结构域。这些结构域与先前认为参与在均匀腱糖蛋白底物上神经突生长的结构域不同。我们得出结论,这两种分子可能促进或阻碍生长锥前进,这取决于空间表达模式和神经元细胞类型。

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