GAP-43:限制神经元的可塑性。

M C Fishman
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摘要

大脑必须在对突触精确度的需求与对环境刺激产生和改变连接模式的能力之间取得平衡。GAP-43是一种与细胞膜细胞质表面相关的磷蛋白,是运输到生长锥的细胞总蛋白的一小部分中最丰富的蛋白之一。它似乎在放大来自微环境的信号方面发挥了不同寻常的作用。完成这项任务的几种方法之一涉及到GAP-43与G蛋白转导级联的相互作用。在同源重组导致GAP-43缺失的小鼠中,一些神经在视交叉等决策点表现出异常生长。因此,GAP-43可能通过信号级联的调制起作用,而不是自主地引起生长,并且可以在产生和维持准确突触连接所需的限制内保持可塑性。
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GAP-43: putting constraints on neuronal plasticity.

The brain must balance the need for synaptic precision with the ability to generate and change connectivity patterns in response to environmental stimuli. GAP-43 is a phosphoprotein associated with the cytosolic surface of the membrane, and is one of the most abundant among the small subset of total cellular proteins transported to the growth cone. It appears to play an unusual role amplifying signals from the microenvironment. One of the several ways to perform this task involves interaction of GAP-43 with the G protein transduction cascade. In mice rendered GAP-43 null by homologous recombination, some nerves manifest aberrant growth at decision points, such as the optic chiasm. Thus, GAP-43 may work via modulation of signaling cascades, rather than autonomously causing growth, and could serve to keep plasticity within constraints needed to generate and maintain accurate synaptic wiring.

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