神经营养因子及其受体:遗传研究的意义

I. Fariñas, L. Reichardt
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引用次数: 32

摘要

编码每一种已知神经营养因子及其受体的基因已经在小鼠中成为目标。正如早期研究预测的那样,每个突变都会导致特定类别的周围神经元的丧失。自然发生的细胞死亡期间的细胞凋亡似乎是造成许多这些损失的原因。在某些情况下,缺陷可能反映了前体增殖、承诺或分化的早期异常。在这些突变体中已经观察到异常靶神经支配和神经元分化的具体例子,这开始被用于解决神经营养蛋白的其他假设功能,如突触功效和可塑性的调节。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neurotrophic factors and their receptors: implications of genetic studies
The genes encoding each of the known neurotrophins and their receptors have been targeted in mice. As predicted by earlier studies, each mutation results in loss of specific classes of peripheral neurons. Apoptosis during the period of naturally occurring cell death appears to be responsible for many of these losses. In some cases, deficits may reflect earlier abnormalities in precursor proliferation, commitment or differentiation. Specific examples of abnormal target innervation and neuronal differentiation have been observed in these mutants, which are beginning to be used to address other postulated functions of neurotrophins, such as modulation of synaptic efficacy and plasticity.
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