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Tubulin cofactor B plays a role in the neuronal growth cone.

机译:微管蛋白辅因子B在神经元生长锥中起作用。

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摘要

Tubulin cofactors, initially identified as alpha-, beta-tubulin folding proteins, are now believed to participate in the complex tubulin biogenesis and degradation routes, and thus to contribute to microtubule functional diversity and dynamics. However, a concrete role of tubulin cofactor B (TBCB) remains to be elucidated because this protein is not required for tubulin biogenesis, and it is apparently not essential for life in any of the organisms studied. In agreement with these data, here we show that TBCB localizes at the transition zone of the growth cones of growing neurites during neurogenesis where it plays a role in microtubule dynamics and plasticity. Gene silencing by means of small interfering RNA segments revealed that TBCB knockdown enhances axonal growth. In contrast, excess TBCB, a feature of giant axonal neuropathy, leads to microtubule depolymerization, growth cone retraction, and axonal damage followed by neuronal degeneration. These results provide an important insight into the understanding of the controlling mechanisms of growth cone microtubule dynamics.
机译:最初被鉴定为α-,β-微管蛋白折叠蛋白的微管蛋白辅因子现在被认为参与了复杂的微管蛋白的生物发生和降解途径,因此有助于微管功能的多样性和动力学。然而,微管蛋白辅因子B(TBCB)的具体作用尚待阐明,因为该蛋白对于微管蛋白的生物发生不是必需的,而且显然对于任何研究的生物来说,生命不是必需的。与这些数据相一致,在这里我们表明TBCB在神经发生过程中位于生长的神经突生长锥的过渡区,在微管动力学和可塑性中起作用。通过小的干扰RNA片段进行的基因沉默显示,TBCB敲低可增强轴突的生长。相反,过量的TBCB是巨大的轴突神经病的特征,导致微管解聚,生长锥缩回和轴突损伤,继而引起神经元变性。这些结果为了解生长锥微管动力学的控制机制提供了重要的见识。

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