Carlson M D, Spooner B S
Differentiation. 1979;13(2):117-23. doi: 10.1111/j.1432-0436.1979.tb01574.x.
Dorsal root ganglia from 8-day chick embryos can be stimulated to extend nerve processes in culture by inclusion of cytosine arabinoside (Ara-C) in the culture medium, in the absence of exogenous nerve growth factor (NGF). The degree of stimulation is dose dependent, and is not mimicked by either free cytosine or free arabinose. Since Ara-C is known to inhibit DNA synthesis, other inhibitors of DNA synthesis were tested. Hydroxyurea, fluorodeoxyuridine, and 3 mM thymidine all stimulated nerve outgrowth in the absence of exogenous NGF. In addition, bromodeoxyuridine also stimulated nerve outgrowth. In all cases, stimulation was observable after 24 h of culture, with maximal outgrowth achieved by 72 h of culture. The experimental response was never as large as the response to NGF, but was up to seven times greater than control outgrowth. In all cultures, nerve processes were characterized by growth cones at their distal tips, colchicine-sensitivity, and a high tubulin content visualized by immunofluorescence with anti-tubulin antibody.
在无外源性神经生长因子(NGF)的情况下,通过在培养基中加入阿糖胞苷(Ara-C),可刺激8日龄鸡胚的背根神经节在培养物中延伸神经突起。刺激程度呈剂量依赖性,游离胞嘧啶或游离阿拉伯糖均无法模拟这种刺激。由于已知Ara-C可抑制DNA合成,因此对其他DNA合成抑制剂进行了测试。羟基脲、氟脱氧尿苷和3 mM胸苷在无外源性NGF的情况下均能刺激神经生长。此外,溴脱氧尿苷也能刺激神经生长。在所有情况下,培养24小时后即可观察到刺激作用,培养72小时时神经突起生长达到最大值。实验反应从未达到对NGF反应的程度,但比对照生长最多大7倍。在所有培养物中,神经突起的特征是其远端末梢有生长锥、对秋水仙碱敏感,并且用抗微管蛋白抗体进行免疫荧光观察时微管蛋白含量很高。