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新型脑特异性连接蛋白Bral2的分子克隆及其与神经周网中短蛋白聚糖的免疫组化共定位

Molecular cloning of Bral2, a novel brain-specific link protein, and immunohistochemical colocalization with brevican in perineuronal nets.

作者信息

Bekku Yoko, Su Wei-Dong, Hirakawa Satoshi, Fässler Reinhard, Ohtsuka Aiji, Kang Jeong Suk, Sanders Jennifer, Murakami Takuro, Ninomiya Yoshifumi, Oohashi Toshitaka

机构信息

Department of Molecular Biology and Biochemistry, Okayama University Graduate School of Medicine and Dentistry, Okayama 700-8558, Japan.

出版信息

Mol Cell Neurosci. 2003 Sep;24(1):148-59. doi: 10.1016/s1044-7431(03)00133-7.

Abstract

The hyaluronan binding chondroitin sulphate proteoglycans, called lecticans, are the abundant extracellular matrix molecules in the developing and/or adult brain. The link proteins (LPs) are also known to be coordinately present in brain. We report here the molecular cloning and expression analysis of a novel member of LPs: Bral2, predominantly expressed in brain. The Bral2 mRNA expression is first detected at P20 and continued through adulthood, suggesting its functional importance and association with adult-type lecticans. The substantial immunoreactivity of Bral2 is found in several nuclei throughout the midbrain and hindbrain in a perineuronal net pattern. In situ hybridization revealed that Bral2 is synthesized by these neurons themselves, especially by the GABAergic neurons in the cerebellar cortex. Interestingly, the colocalization and synergic importance of Bral2 and brevican in the perineuronal nets is indicated by the comparative immunohistochemical analysis using wild-type and brevican-deficient mouse brain. Our results suggest that Bral2 is involved in the formation of extracellular matrix contributing to perineuronal nets and facilitate the understanding of a functional role of these extracellular matrices.

摘要

称为凝集素的透明质酸结合硫酸软骨素蛋白聚糖是发育中和/或成体大脑中丰富的细胞外基质分子。已知连接蛋白(LPs)也协同存在于大脑中。我们在此报告一种新型连接蛋白成员Bral2的分子克隆和表达分析,其主要在大脑中表达。Bral2 mRNA表达首先在出生后20天被检测到,并持续至成年期,表明其功能重要性以及与成年型凝集素的关联。在中脑和后脑的几个核中以神经元周围网络模式发现了Bral2的大量免疫反应性。原位杂交显示Bral2由这些神经元自身合成,尤其是小脑皮质中的γ-氨基丁酸能神经元。有趣的是,使用野生型和短蛋白聚糖缺陷型小鼠脑的比较免疫组织化学分析表明了Bral2和短蛋白聚糖在神经元周围网络中的共定位和协同重要性。我们的结果表明,Bral2参与了有助于神经元周围网络的细胞外基质的形成,并有助于理解这些细胞外基质的功能作用。

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