The role of glial cells in influencing neurite extension by dorsal root ganglion cells.

Neuron glia biology Pub Date : 2010-02-01 Epub Date: 2009-12-22 DOI:10.1017/S1740925X09990433
Kai-Yu Ng, Yung H Wong, Helen Wise
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引用次数: 10

Abstract

When pretreated with pertussis toxin (PTX), the neurites of adult rat dorsal root ganglion (DRG) cells in mixed cell cultures retract over a period of 2 h following the initial stimulus of removal from the cell culture incubator for brief periods of observation. The purpose of this investigation was to determine whether this PTX-dependent response was specific to any one of the three subpopulations of DRG neurons. However, no neurite retraction response was observed in neuron-enriched populations of cells, or in cultures enriched in isolectin B4 (IB4)-positive neurons or in IB4-negative neurons. But, the addition of non-neuronal cells, and/or medium conditioned by non-neuronal cells, was sufficient to restore the PTX-dependent neurite retraction response, but only in large diameter IB4-negative neurons. In conclusion, we have identified a regulatory response, mediated by Gi/o-proteins, which prevents retraction of neurites in large diameter IB4-negative cells of adult rat DRG. The non-neuronal cells of adult rat DRG constitutively release factor/s that can stimulate neurite retraction of a subset of isolated DRG neurons, but this property of non-neuronal cells is only observed when the Gi/o-proteins of large diameter IB4-negative cells are inhibited.

神经胶质细胞在影响背根神经节细胞的神经突延伸中的作用。
当用百日毒(PTX)预处理时,混合细胞培养中成年大鼠背根神经节(DRG)细胞的神经突在最初的刺激下从细胞培养箱中取出进行短暂的观察后2小时内收缩。这项研究的目的是确定这种ptx依赖性反应是否特异性于DRG神经元的三个亚群中的任何一个。然而,在富含神经元的细胞群体中,或在富含隔离素B4 (IB4)阳性神经元或IB4阴性神经元的培养物中,均未观察到神经突缩回反应。但是,添加非神经元细胞和/或由非神经元细胞调节的培养基足以恢复ptx依赖性神经突收缩反应,但仅限于大直径ib4阴性神经元。总之,我们发现了一种由Gi/o蛋白介导的调节反应,可以阻止成年大鼠DRG大直径ib4阴性细胞的神经突缩回。成年大鼠DRG的非神经元细胞组成性释放因子/s,可以刺激一部分分离的DRG神经元的神经突收缩,但非神经元细胞的这种特性仅在大直径ib4阴性细胞的Gi/o蛋白被抑制时才观察到。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neuron glia biology
Neuron glia biology 医学-神经科学
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