Mattson M P, Guthrie P B, Kater S B
Department of Anatomy and Neurobiology, Colorado State University, Fort Collins 80523.
J Neurosci Res. 1988 Jul;20(3):331-45. doi: 10.1002/jnr.490200307.
The present study examined the cellular mechanisms underlying the generation of neuroarchitecture. Identified Helisoma neurons in isolated cell culture normally require factors present in brain-conditioned medium (CM) in order to display the different components of neurite outgrowth (sprouting, elongation, branching, and growth cone motility), which ultimately determine their overall architecture. We report here that cell calcium and cell-substrate interactions can play quite specific roles in the regulation of these different components of neuronal outgrowth. CM-induced neurite outgrowth was inhibited by calcium ionophore A23187. In the absence of CM the calcium channel blocker La3+ (10 microM) reduced intracellular calcium levels and induced neurite sprouting and elongation; growth cone motility and branching were greatly reduced in the La3+-induced neurites. Neurons plated into an environment containing La3+ and a fibronectin substrate exhibited all of the components of neuronal outgrowth normally seen in response to CM. Fibronectin alone had little outgrowth-promoting activity. Neurite elongation rates and branching were increased by exposure to La3+ in neurons on either a CM or fibronectin substrate. The neurons growing on CM or fibronectin whose outgrowth was accelerated by La3+ elaborated neuritic arbors that differed from those of neurons grown in response to CM; differences were seen in neurite length, area of outgrowth, branching frequency, and varicosity numbers. Taken together, these results indicate that 1) calcium and the growth substrate can exert specific effects on neurite sprouting, elongation, growth cone motility, and branching; 2) appropriate levels of activation of these two systems can elicit neurite outgrowth that closely resembles that induced by endogenous growth factors; 3) both the differential expression of the separate components of outgrowth and the kinetics of outgrowth determine a neuron's morphology.
本研究探讨了神经结构形成背后的细胞机制。在分离的细胞培养物中,已鉴定的椎实螺神经元通常需要脑条件培养基(CM)中存在的因子,以便展现出神经突生长的不同组成部分(发芽、伸长、分支和生长锥运动),这些最终决定了它们的整体结构。我们在此报告,细胞钙和细胞 - 底物相互作用在调节神经元生长的这些不同组成部分中可发挥相当特定的作用。CM诱导的神经突生长受到钙离子载体A23187的抑制。在没有CM的情况下,钙通道阻滞剂La3 +(10 microM)降低细胞内钙水平并诱导神经突发芽和伸长;在La3 +诱导的神经突中,生长锥运动和分支大大减少。接种到含有La3 +和纤连蛋白底物的环境中的神经元表现出通常在对CM反应中看到的神经元生长的所有组成部分。单独的纤连蛋白几乎没有促进生长的活性。在CM或纤连蛋白底物上的神经元中,暴露于La3 +会增加神经突伸长率和分支。在CM或纤连蛋白上生长且其生长因La3 +而加速的神经元形成的神经树突与对CM反应生长的神经元不同;在神经突长度、生长面积、分支频率和曲张数方面存在差异。综上所述,这些结果表明:1)钙和生长底物可对神经突发芽、伸长、生长锥运动和分支产生特定影响;2)这两个系统的适当激活水平可引发与内源性生长因子诱导的神经突生长非常相似;3)生长各组成部分的差异表达和生长动力学都决定了神经元的形态。