Rho家族gtpase激活蛋白Rich2/Arhgap44在小鼠脑发育过程中的表达分析

IF 2.3 4区 医学 Q2 DEVELOPMENTAL BIOLOGY
Naoki Goto, Masashi Nishikawa, Hidenori Ito, Mariko Noda, Nanako Hamada, Hidenori Tabata, Makoto Kinoshita, Koh-Ichi Nagata
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引用次数: 3

摘要

Rho家族小gtp酶,如Rho、Rac和Cdc42,通过调节细胞信号传导和肌动蛋白细胞骨架重组,在大脑发育过程中发挥重要作用。Rich2/Arhgap44是一种Rac-和cdc42特异性gtpase激活蛋白,已被报道为树突棘形态和突触功能的关键调节因子。考虑到Rac和Cdc42在大脑发育中的重要作用,Rich2被认为参与了大脑发育。然而,Rich2在神经发育过程中的表达谱及相关分子机制尚不清楚。在本研究中,我们以小鼠大脑发育为重点,对Rich2进行了表达分析。在免疫印迹中,Rich2在年轻成年小鼠中表现出组织依赖性的表达谱,并且在大脑发育过程中表达增加。免疫组化分析显示,Rich2在出生后第0天(P)在皮质神经元细胞质中观察到,然后在P7时开始在细胞核中富集,并在神经粒中有中等分布。P30后,观察到Rich2的复杂免疫染色模式;Rich2在许多皮质神经元中分布于细胞核、细胞质和神经丸中,而其他神经元通常很少表达。在P7海马中,Rich2主要分布在角状氨区兴奋性神经元的细胞质中,而在齿状颗粒细胞的细胞核中也有少量检测到。值得注意的是,Rich2分布在羊角氨1区的兴奋性突触中。生化分离分析也在突触后密度中检测到Rich2。综上所述,Rich2在中枢神经系统中以发育阶段依赖的方式表达,并可能参与皮层神经元突触的形成/维持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Expression Analyses of Rich2/Arhgap44, a Rho Family GTPase-Activating Protein, during Mouse Brain Development.

Expression Analyses of Rich2/Arhgap44, a Rho Family GTPase-Activating Protein, during Mouse Brain Development.

Expression Analyses of Rich2/Arhgap44, a Rho Family GTPase-Activating Protein, during Mouse Brain Development.

Expression Analyses of Rich2/Arhgap44, a Rho Family GTPase-Activating Protein, during Mouse Brain Development.

Rho family small GTPases, such as Rho, Rac, and Cdc42, play essential roles during brain development, by regulating cellular signaling and actin cytoskeletal reorganization. Rich2/Arhgap44, a Rac- and Cdc42-specific GTPase-activating protein, has been reported to be a key regulator for dendritic spine morphology and synaptic function. Given the essential roles of Rac and Cdc42 in brain development, Rich2 is supposed to take part in brain development. However, not only the molecular mechanism involved but also the expression profile of Rich2 during neurodevelopment has not yet been elucidated. In this study, we carried out expression analyses of Rich2 by focusing on mouse brain development. In immunoblotting, Rich2 exhibited a tissue-dependent expression profile in the young adult mouse, and the expression was increased during brain development. In immunohistochemical analyses, Rich2 was observed in the cytoplasm of cortical neurons at postnatal day (P) 0 and then came to be enriched in the nucleus with moderate distribution in neuropils at P7. Later at P30, a complex immunostaining pattern of Rich2 was observed; Rich2 was distributed in the nucleus, cytoplasm, and neuropils in many cortical neurons, whereas other neurons frequently displayed little expression. In the hippocampus at P7, Rich2 was distributed mainly in the cytoplasm of excitatory neurons in the cornu ammonis regions, while it was moderately detected in the nucleus in the dentate granule cells. Notably, Rich2 was distributed in excitatory synapses of the cornu ammonis 1 region at P30. Biochemical fractionation analyses also detected Rich2 in the postsynaptic density. Taken together, Rich2 is found to be expressed in the central nervous system in a developmental stage-dependent manner and may be involved in synapse formation/maintenance in cortical neurons.

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来源期刊
Developmental Neuroscience
Developmental Neuroscience 医学-发育生物学
CiteScore
4.00
自引率
3.40%
发文量
49
审稿时长
>12 weeks
期刊介绍: ''Developmental Neuroscience'' is a multidisciplinary journal publishing papers covering all stages of invertebrate, vertebrate and human brain development. Emphasis is placed on publishing fundamental as well as translational studies that contribute to our understanding of mechanisms of normal development as well as genetic and environmental causes of abnormal brain development. The journal thus provides valuable information for both physicians and biologists. To meet the rapidly expanding information needs of its readers, the journal combines original papers that report on progress and advances in developmental neuroscience with concise mini-reviews that provide a timely overview of key topics, new insights and ongoing controversies. The editorial standards of ''Developmental Neuroscience'' are high. We are committed to publishing only high quality, complete papers that make significant contributions to the field.
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