The non-mitotic role of HMMR in regulating the localization of TPX2 and the dynamics of microtubules in neurons

Yi-Ru Chen, Shun-Cheng Tseng, Eric Hwang
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Abstract

A functional nervous system is built upon the proper morphogenesis of neurons to establish the intricate connection between them. The microtubule cytoskeleton is known to play various essential roles in this morphogenetic process. While many microtubule-associated proteins (MAPs) have been demonstrated to participate in neuronal morphogenesis, the function of many more remains to be determined. This study focuses on a MAP called HMMR, which was originally identified as a hyaluronan binding protein and later found to possess microtubule and centrosome binding capacity. HMMR exhibits high abundance on neuronal microtubules and altering the level of HMMR significantly affects the morphology of neurons. Instead of confining to the centrosome(s) like cells in mitosis, HMMR localizes to microtubules along axons and dendrites. Furthermore, transiently expressing HMMR enhances the stability of neuronal microtubules and increases the formation frequency of growing microtubules along the neurites. HMMR regulates the microtubule localization of a non-centrosomal microtubule nucleator TPX2 along the neurite, offering an explanation for how HMMR contributes to the promotion of growing microtubules. This study sheds light on how progenitor cells utilize proteins involved in mitosis for non-mitotic functions.
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HMMR在调控TPX2定位和神经元微管动力学中的非有丝分裂作用
一个功能性的神经系统是建立在神经元的适当形态上的,以建立它们之间复杂的联系。已知微管细胞骨架在这一形态发生过程中起着各种重要作用。虽然许多微管相关蛋白(MAPs)已被证明参与神经元的形态发生,但更多的功能仍有待确定。本研究的重点是一种名为HMMR的MAP,它最初被确定为透明质酸结合蛋白,后来发现具有微管和中心体的结合能力。HMMR在神经元微管上表现出高丰度,改变HMMR的水平会显著影响神经元的形态。在有丝分裂中,HMMR不局限于中心体细胞,而是定位于沿轴突和树突的微管。瞬时表达HMMR增强了神经元微管的稳定性,增加了沿神经突生长的微管的形成频率。HMMR调节非中心体微管核子TPX2沿神经突的微管定位,为HMMR如何促进微管生长提供了解释。本研究揭示了祖细胞如何利用参与有丝分裂的蛋白实现非有丝分裂功能。
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