Dissecting Growth Cone Guidance

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Abstract

The growth cones of developing neurons take s and turns that allow them to reach the appropriate target. Their path is guided by responses to attractive and repulsive cues from chemotropic ligands that they encounter along the way. These ligands activate receptors on the surface of the growth cone. Campbell and Holt describe new insights into the signaling pathways that are integrated to process such guidance cues. They report that in cultured Xenopus retinal growth cones, three different chemotropic ligands, netrin-1, semaphorin3A (Sema3A), and lysophosphatidic acid (LPA) stimulate distinct, but overlapping, signaling pathways. Netrin-1 and Sema3A activated the p42 and p44 mitogen-activated protein kinases (MAPKs). The p38 MAPK, normally associated with stress responses, was activated in cells treated with netrin-1 or LPA. Experiments with pharmacological inhibitors of the kinases indicated that the MAPK responses were necessary for axon guidance. Studies with antibodies to the active, cleaved form of caspase-3 revealed that caspase-3 was activated in response to LPA or netrin-1, and again, inhibitors were used to show that caspase activity was required for chemotropic responses in vitro. The authors discuss the potential role of caspase-3--better known as a component of pathways leading to apoptosis or cell death--in axon guidance. The authors further note similarities between the chemotropic pathways implicated in the present work with those thought to regulate synaptic plasticity. C. S. Campbell, C. E. Holt, Apoptotic pathway and MAPKs differentially regulate chemotropic responses of retinal growth cones. Neuron 37, 939-952 (2003). [Online Journal]
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解剖生长锥引导
发育中的神经元的生长锥需要5个周期才能到达合适的目标。它们的路径是通过对沿途遇到的趋化配体的吸引和排斥信号的反应来引导的。这些配体激活生长锥表面的受体。坎贝尔和霍尔特描述了对信号通路的新见解,这些信号通路被整合到处理这些指导线索中。他们报告说,在培养的非洲爪蟾视网膜生长锥中,三种不同的趋化配体,netrin-1, Sema3A (Sema3A)和溶血磷脂酸(LPA)刺激不同但重叠的信号通路。Netrin-1和Sema3A激活p42和p44分裂原活化蛋白激酶(MAPKs)。通常与应激反应相关的p38 MAPK在用netrin-1或LPA处理的细胞中被激活。激酶的药理抑制剂实验表明,MAPK反应是轴突引导所必需的。对caspase-3的活性,裂解形式的抗体的研究表明,caspase-3在LPA或netrin-1的反应中被激活,并且再次使用抑制剂来表明caspase活性是体外趋化反应所必需的。作者讨论了caspase-3在轴突引导中的潜在作用,caspase-3是导致细胞凋亡或细胞死亡的途径的一个组成部分。作者进一步指出,在本研究中涉及的趋化通路与那些被认为调节突触可塑性的通路之间存在相似之处。黄春华,黄春华。细胞凋亡通路和MAPKs对视网膜生长锥细胞趋化反应的调控。神经元37,939-952(2003)。(在线期刊)
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