Campenot R B, Draker D D
Department of Anatomy and Cell Biology, Faculty of Medicine, University of Alberta, Edmonton, Canada.
Neuron. 1989 Dec;3(6):733-43. doi: 10.1016/0896-6273(89)90242-0.
A compartmented culture system in which distal neurites from newborn rat sympathetic neurons entered a fluid environment separate from that bathing the cell bodies and proximal neurites was used to investigate effects of extracellular Ca2+ deprivation on nerve fiber growth. Neurites readily grew into, elongated for many days within, and regenerated after neuritotomy within distal compartments substantially deprived of Ca2+ (0 added Ca2+, 0.5-5 mM EGTA), provided Ca2+ was supplied to the cell bodies. The Ca2(+)-deprived neurites generally extended at rates 20%-35% slower than controls. Growth of neurites did, however, cease within 2 days when the cell bodies were deprived of Ca2+, and the neurites and cell bodies eventually degenerated. These results show that neither extracellular Ca2+ nor the influx of Ca2+ at or near the growth cone is required for sustained neurite growth. They also rule out the possibility that the promotion of neurite growth by nerve growth factor is mediated, by the influx of extracellular Ca2+.
一种分隔培养系统被用于研究细胞外钙剥夺对神经纤维生长的影响,在该系统中,新生大鼠交感神经元的远端神经突进入一个与细胞体和近端神经突所处浴液环境分开的液体环境。只要向细胞体提供钙离子,神经突就能很容易地生长进入、在基本上没有钙离子(未添加钙离子,0.5 - 5 mM乙二醇双四乙酸)的远端分隔区域内延伸许多天,并在神经突切断后再生。与对照组相比,缺乏钙离子的神经突通常以慢20% - 35%的速度延伸。然而,当细胞体缺乏钙离子时,神经突的生长在2天内就会停止,神经突和细胞体最终会退化。这些结果表明,持续的神经突生长既不需要细胞外钙离子,也不需要生长锥处或其附近的钙离子内流。它们还排除了神经生长因子促进神经突生长是由细胞外钙离子内流介导的可能性。