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PACT/RAX调节发育中小脑中小脑颗粒神经元的迁移。

PACT/RAX regulates the migration of cerebellar granule neurons in the developing cerebellum.

作者信息

Yong Yue, Meng Ya, Ding Hanqing, Fan Zhiqin, Tang Yifen, Zhou Chenghua, Luo Jia, Ke Zun-Ji

机构信息

1] Department of Biochemistry, Shanghai University of Traditional Chinese Medicine, 1200 Cailun Road, Shanghai 201203, China [2] Key Laboratory of Nutrition and Metabolism, Institute for Nutritional Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Graduate School of the Chinese Academy of Sciences, Shanghai 200031, China.

Department of Biochemistry, Shanghai University of Traditional Chinese Medicine, 1200 Cailun Road, Shanghai 201203, China.

出版信息

Sci Rep. 2015 Jan 22;5:7961. doi: 10.1038/srep07961.

Abstract

PACT and its murine ortholog RAX were originally identified as a protein activator for the dsRNA-dependent, interferon-inducible protein kinase PKR. Recent studies indicated that RAX played a role in embryogenesis and neuronal development. In this study, we investigated the expression of RAX during the postnatal development of the mouse cerebellum and its role in the migration of cerebellar granule neurons (CGNs). High expression of RAX was observed in the cerebellum from postnatal day (PD) 4 to PD9, a period when the CGNs migrate from the external granule layer (EGL) to the internal granule layer (IGL). The migration of the EGL progenitor cells in vivo was inhibited by RAX knockdown on PD4. This finding was confirmed by in vitro studies showing that RAX knockdown impaired the migration of CGNs in cerebellar microexplants. PACT/RAX-regulated migration required its third motif and was independent of PKR. PACT/RAX interacted with focal adhesion kinase (FAK) and PACT/RAX knockdown disturbed the FAK phosphorylation in CGNs. These findings demonstrated a novel function of PACT/RAX in the regulation of neuronal migration.

摘要

PACT及其小鼠同源物RAX最初被鉴定为双链RNA依赖性干扰素诱导蛋白激酶PKR的蛋白激活剂。最近的研究表明,RAX在胚胎发生和神经元发育中发挥作用。在本研究中,我们研究了RAX在小鼠小脑出生后发育过程中的表达及其在小脑颗粒神经元(CGNs)迁移中的作用。在出生后第4天(PD)至第9天的小脑中观察到RAX的高表达,这一时期CGNs从外颗粒层(EGL)迁移到内颗粒层(IGL)。在PD4时,RAX敲低可抑制体内EGL祖细胞的迁移。体外研究证实了这一发现,表明RAX敲低会损害小脑微植块中CGNs的迁移。PACT/RAX调节的迁移需要其第三个基序,且独立于PKR。PACT/RAX与粘着斑激酶(FAK)相互作用,PACT/RAX敲低会干扰CGNs中的FAK磷酸化。这些发现证明了PACT/RAX在调节神经元迁移中的新功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44ad/4302322/a686db50d387/srep07961-f1.jpg

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