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神经胶质细胞的排列在体外刺激中枢神经系统神经元的定向轴突生长。

Alignment of glial cells stimulates directional neurite growth of CNS neurons in vitro.

作者信息

Deumens R, Koopmans G C, Den Bakker C G J, Maquet V, Blacher S, Honig W M M, Jérôme R, Pirard J-P, Steinbusch H W M, Joosten E A J

机构信息

Department of Psychiatry and Neuropsychology, European Graduate School for Neuroscience (EURON), Universiteit Maastricht, PO Box 616, 6200 MD, Maastricht, The Netherlands.

出版信息

Neuroscience. 2004;125(3):591-604. doi: 10.1016/j.neuroscience.2004.02.010.

Abstract

Olfactory ensheathing cells (OECs) together with olfactory nerve fibroblasts (ONFs) and neonatal astrocytes are potent stimulators of neurite growth in adulthood and during development, respectively. Since it is known that alignment of glial cells is important for the correct outgrowth of axon tracts, it was hypothesized that the alignment of glial cells stimulates directional and enhanced neurite outgrowth. Adult OEC/ONF and neonatal astrocytes were cultured either on biodegradable poly(d,l)-lactide matrices or in Petri dishes for 4 days. Thereafter neonatal cerebral cortical neurons were added. After a 2-days coculture period the cultures were fixed and processed for a combined MAP-2 and phosphorylated neurofilament (RT97) staining. The neurite growth (neurite elongation and neurite formation) and the neurite direction were assessed. We show that (1). OEC/ONF cultures are more potent in stimulating the length of the longest neurite of cocultured neurons, (2). alignment of glial is achieved in vitro on our biomatrices, (3). aligned glial/biomatrix complexes do not enhance neurite growth, and (4). aligned glial/biomatrix complexes direct neurite outgrowth. These data have significant implications for in vivo experiments focusing on glial transplantation. Transplanting glial/biomatrix complexes may stimulate the directional regrowth of severed axons across a lesion site.

摘要

嗅鞘细胞(OECs)与嗅神经成纤维细胞(ONFs)以及新生星形胶质细胞分别是成年期和发育期间神经突生长的有效刺激物。由于已知神经胶质细胞的排列对于轴突束的正确生长很重要,因此有人推测神经胶质细胞的排列会刺激定向且增强的神经突生长。将成年OEC/ONF和新生星形胶质细胞在可生物降解的聚(d,l)-丙交酯基质上或在培养皿中培养4天。此后加入新生大脑皮质神经元。经过2天的共培养期后,将培养物固定并进行联合的微管相关蛋白2(MAP-2)和磷酸化神经丝(RT97)染色处理。评估神经突生长(神经突伸长和神经突形成)以及神经突方向。我们发现:(1)。OEC/ONF培养物在刺激共培养神经元最长神经突的长度方面更有效;(2)。在我们的生物基质上可在体外实现神经胶质细胞的排列;(3)。排列的神经胶质/生物基质复合物不会增强神经突生长;(4)。排列的神经胶质/生物基质复合物引导神经突生长。这些数据对于专注于神经胶质细胞移植的体内实验具有重要意义。移植神经胶质/生物基质复合物可能会刺激切断的轴突在损伤部位进行定向再生。

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