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培养中非神经元细胞对神经突的引导作用:与非神经胶质细胞表面相比,周围神经突在神经胶质细胞表面优先生长。

Neurite guidance by non-neuronal cells in culture: preferential outgrowth of peripheral neurites on glial as compared to nonglial cell surfaces.

作者信息

Fallon J R

出版信息

J Neurosci. 1985 Dec;5(12):3169-77. doi: 10.1523/JNEUROSCI.05-12-03169.1985.

Abstract

Growing axons in the peripheral nervous system (PNS) encounter a variety of cellular and extracellular substrates. Since it is difficult to sort out the possible contributions of these diverse components of the extracellular environment to axonal guidance in vivo, I have developed an in vitro system to study neurite outgrowth on two classes of cells which may provide as substrates for growing axons during development or regeneration: glial cells, e.g., astrocytes and Schwann cells, and nonglial cells, e.g., fibroblasts. Although neurites from sympathetic and spinal sensory ganglia explants grew onto preformed monolayers of both glial and nonglial cells, glial cells were a markedly better substrate. On the glial cells the neurites extended at a rate of 25 to 30 micron/hr and traveled singly or in fine fascicles; their growth cones displayed long filopodia and migrated on the upper surface of the monolayer cells. Conditioned media experiments suggested that neurite outgrowth on glial cell monolayers was not mediated by soluble secreted factors. These results indicate that the glial cell surface is an attractive substrate for neurite outgrowth. In contrast, on nonglial cells the rate of outgrowth was only 10 to 15 micron/hr, large neurite fascicles were common, and the growth cones migrated beneath the monolayer cells in contact with the underlying artificial substrate. This location of the growth cone, coupled with the observation that conditioned medium from these cells promoted neurite outgrowth only when bound to artificial substrates, suggests that secreted substrate-associated components may be an important determinant of neurite outgrowth on nonglial cell monolayers.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

外周神经系统(PNS)中正在生长的轴突会遇到多种细胞和细胞外基质。由于很难在体内区分细胞外环境的这些不同成分对轴突导向可能产生的作用,我开发了一种体外系统,以研究神经突在两类细胞上的生长情况,这两类细胞在发育或再生过程中可能作为生长轴突的基质:胶质细胞,如星形胶质细胞和雪旺细胞,以及非胶质细胞,如成纤维细胞。虽然来自交感神经节和脊髓感觉神经节外植体的神经突生长到了胶质细胞和非胶质细胞预先形成的单层上,但胶质细胞是明显更好的基质。在胶质细胞上,神经突以25至30微米/小时的速度延伸,单独或成细束状行进;它们的生长锥显示出长的丝状伪足,并在单层细胞的上表面迁移。条件培养基实验表明,胶质细胞单层上的神经突生长不是由可溶性分泌因子介导的。这些结果表明,胶质细胞表面是神经突生长的有吸引力的基质。相比之下,在非胶质细胞上,生长速度仅为10至15微米/小时,大的神经突束很常见,并且生长锥在与下面的人工基质接触的单层细胞下方迁移。生长锥的这种位置,加上观察到来自这些细胞的条件培养基仅在与人工基质结合时才促进神经突生长,表明分泌的与基质相关的成分可能是非胶质细胞单层上神经突生长的重要决定因素。(摘要截短至250字)

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