Wood P M, Bunge R P
Nature. 1986;320(6064):756-8. doi: 10.1038/320756a0.
Recovery from demyelinating events in the adult central nervous system (CNS) may depend in some situations on the generation, by cell division, of new oligodendrocytes (ODCs). Adult ODCs, identified by morphological criteria, have been shown to divide in vivo in response to induced demyelination or to physical trauma, although the factors that elicit this response are unknown. Adult ODCs do not proliferate in vitro under normal conditions (ref. 4 and P.M.W., unpublished observations). Encouraged by observations that axons provide a mitogenic stimulus for Schwann cells and support the proliferation of embryonic ODC progenitors, we have studied the response of adult ODCs, identified by immunocytological criteria, to axons of dorsal root ganglion neurones in culture. We have now found that adult ODCs proliferate in vitro when neurones are present but not when neurones are absent, suggesting that neurons can elicit ODC division under the conditions prevailing in our culture system.
在某些情况下,成体中枢神经系统(CNS)脱髓鞘事件的恢复可能依赖于通过细胞分裂产生新的少突胶质细胞(ODC)。通过形态学标准鉴定的成体ODC已被证明在体内会因诱导性脱髓鞘或物理创伤而发生分裂,尽管引发这种反应的因素尚不清楚。在正常条件下,成体ODC在体外不会增殖(参考文献4以及P.M.W.未发表的观察结果)。鉴于轴突为雪旺细胞提供有丝分裂刺激并支持胚胎ODC祖细胞增殖的观察结果,我们研究了通过免疫细胞化学标准鉴定的成体ODC对培养的背根神经节神经元轴突的反应。我们现在发现,当有神经元存在时,成体ODC在体外会增殖,而当没有神经元时则不会,这表明在我们的培养系统所存在的条件下,神经元能够引发ODC分裂。