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近端轴突中的驱动蛋白调节对于树突选择性运输至关重要。

Kinesin Regulation in the Proximal Axon is Essential for Dendrite-selective Transport.

机构信息

Department of Biological Sciences and the Center for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute, Troy, NY 12180.

Jungers Center for Neurosciences Research, Oregon Health & Science University, Portland, Oregon 97239.

出版信息

Mol Biol Cell. 2024 Jun 1;35(6):ar81. doi: 10.1091/mbc.E23-11-0457. Epub 2024 Apr 10.

Abstract

Neurons are polarized and typically extend multiple dendrites and one axon. To maintain polarity, vesicles carrying dendritic proteins are arrested upon entering the axon. To determine whether kinesin regulation is required for terminating anterograde axonal transport, we overexpressed the dendrite-selective kinesin KIF13A. This caused mistargeting of dendrite-selective vesicles to the axon and a loss of dendritic polarity. Polarity was not disrupted if the kinase MARK2/Par1b was coexpressed. MARK2/Par1b is concentrated in the proximal axon, where it maintains dendritic polarity-likely by phosphorylating S1371 of KIF13A, which lies in a canonical 14-3-3 binding motif. We probed for interactions of KIF13A with 14-3-3 isoforms and found that 14-3-3β and 14-3-3ζ bound KIF13A. Disruption of MARK2 or 14-3-3 activity by small molecule inhibitors caused a loss of dendritic polarity. These data show that kinesin regulation is integral for dendrite-selective transport. We propose a new model in which KIF13A that moves dendrite-selective vesicles in the proximal axon is phosphorylated by MARK2. Phosphorylated KIF13A is then recognized by 14-3-3, which causes dissociation of KIF13A from the vesicle and termination of transport. These findings define a new paradigm for the regulation of vesicle transport by localized kinesin tail phosphorylation, to restrict dendrite-selective vesicles from entering the axon.

摘要

神经元具有极性,通常会延伸出多个树突和一个轴突。为了维持极性,进入轴突的携带树突蛋白的囊泡会被捕获。为了确定是否需要驱动蛋白调节来终止顺行轴突运输,我们过表达了树突选择性驱动蛋白 KIF13A。这导致树突选择性囊泡错误靶向轴突,并丧失树突极性。如果共表达激酶 MARK2/Par1b,则不会破坏极性。MARK2/Par1b 集中在轴突的近端,在那里通过磷酸化位于经典 14-3-3 结合基序中的 KIF13A 的 S1371 来维持树突极性。我们探测了 KIF13A 与 14-3-3 同工型的相互作用,并发现 14-3-3β 和 14-3-3ζ 与 KIF13A 结合。小分子抑制剂对 MARK2 或 14-3-3 活性的破坏导致树突极性丧失。这些数据表明,驱动蛋白调节对于树突选择性运输是必不可少的。我们提出了一个新模型,其中在轴突近端移动树突选择性囊泡的 KIF13A 被 MARK2 磷酸化。磷酸化的 KIF13A 然后被 14-3-3 识别,这导致 KIF13A 与囊泡解离并终止运输。这些发现定义了一个新的范例,即通过局部驱动蛋白尾部磷酸化来调节囊泡运输,以防止树突选择性囊泡进入轴突。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a5e/11238084/f21033ccf8c8/mbc-35-ar81-g001.jpg

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