Delrée P, Ribbens C, Martin D, Rogister B, Lefebvre P P, Rigo J M, Leprince P, Schoenen J, Moonen G
Human Physiology and Pathophysiology, Université de Liege, Institut Léon Frédéricq, Belgium.
Brain Res Bull. 1993;30(3-4):231-7. doi: 10.1016/0361-9230(93)90249-b.
We review recent data on the plasticity of dorsal root ganglion (DRG) neurons as revealed during cultivation in vitro. Some experiments on cultured developing DRG neurons and on adult DRG neurons in vivo are also mentioned. Cultured developing and adult DRG neurons can be switched from an apolar to a multipolar phenotype by fetal calf serum or fibronectin. The effect is concentration dependent and occurs through an early modification of cell-substratum interaction. Adult DRG neurons synthesize and release within hours after injury TGF beta-1, which is a mitogen and a differentiation factor for Schwann cells. Finally, adult DRG neurons express in vitro neurotransmitters that are not expressed in vivo. This neurotransmitter plasticity can be modulated in vitro by some growth factors and in vivo by distal or proximal axotomy.
我们回顾了有关背根神经节(DRG)神经元在体外培养过程中所显示出的可塑性的最新数据。文中还提及了一些针对培养中的发育中DRG神经元以及成年DRG神经元在体内的实验。培养中的发育中DRG神经元和成年DRG神经元可通过胎牛血清或纤连蛋白从无极表型转变为多极表型。这种效应具有浓度依赖性,并且是通过对细胞与基质相互作用的早期修饰而发生的。成年DRG神经元在损伤后数小时内合成并释放转化生长因子β-1(TGF beta-1),它是雪旺细胞的有丝分裂原和分化因子。最后,成年DRG神经元在体外表达体内未表达的神经递质。这种神经递质可塑性在体外可由某些生长因子调节,在体内可由远端或近端轴突切断调节。