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边缘系统相关膜蛋白(LAMP)选择性地介导与特定中枢神经元群体的相互作用。

The limbic system-associated membrane protein (LAMP) selectively mediates interactions with specific central neuron populations.

作者信息

Zhukareva V, Levitt P

机构信息

Department of Neuroscience and Cell Biology, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School, Piscataway 08854, USA.

出版信息

Development. 1995 Apr;121(4):1161-72. doi: 10.1242/dev.121.4.1161.

Abstract

The limbic system-associated membrane protein (LAMP) is a 64-68 x 10(3) M(r) glycoprotein that is expressed by subsets of neurons that are functionally interconnected. LAMP exhibits characteristics that are indicative of a developmentally significant protein, such as an early and restricted pattern of expression and the ability to mediate specific fiber-target interactions. A potential, selective adhesive mechanism by which LAMP may regulate the formation of specific circuits is investigated in the present experiments. LAMP is readily released from intact membranes by phosphatidyl inositol-specific phospholipase C. Purified, native LAMP, isolated by PI-PLC digestion and immunoaffinity chromatography, is capable of mediating fluorescent Covasphere aggregation via homophilic binding. To test the ability of LAMP to selectively facilitate substrate adhesion and growth of neurons from LAMP-positive, in contrast to LAMP-negative regions of the developing brain, purified LAMP was dotted onto nitrocellulose-coated dishes and test cells plated. Limbic neurons from perirhinal cortex bind specifically to substrate-bound LAMP within 4 hours, forming small cell aggregates with short neuritic processes that continue to grow through a 48 hour period of monitoring. Preincubation of cells with anti-LAMP has a modest effect on cell binding but significantly reduces initiation of process growth. Non-limbic neurons from somatosensory cortex and olfactory bulb fail to bind or extend processes on the LAMP substrate to any significant extent. All cell populations bind equally well and form neurites on poly-D-lysine and laminin. The present results provide direct evidence that LAMP can specifically facilitate interactions with select neurons in the CNS during development. The data support the concept that patterned expression of unique cell adhesion molecules in functionally related regions of the mammalian brain can regulate circuit formation.

摘要

边缘系统相关膜蛋白(LAMP)是一种分子量为64 - 68×10³的糖蛋白,由功能上相互连接的神经元亚群表达。LAMP表现出一些表明其在发育中具有重要意义的特征,例如早期且受限的表达模式以及介导特定纤维 - 靶标相互作用的能力。在本实验中,研究了LAMP可能调节特定回路形成的一种潜在的选择性黏附机制。LAMP很容易被磷脂酰肌醇特异性磷脂酶C从完整膜上释放出来。通过PI - PLC消化和免疫亲和层析分离得到的纯化天然LAMP,能够通过同源结合介导荧光共聚球聚集。为了测试LAMP与发育中脑的LAMP阳性区域而非LAMP阴性区域的神经元相比,选择性促进底物黏附及生长的能力,将纯化的LAMP点在硝酸纤维素包被的培养皿上,然后接种测试细胞。来自梨状周围皮质的边缘神经元在4小时内特异性结合到结合在底物上的LAMP,形成具有短神经突起的小细胞聚集体,在48小时的监测期内这些突起持续生长。用抗LAMP对细胞进行预孵育对细胞结合有一定影响,但显著减少突起生长的起始。来自体感皮质和嗅球的非边缘神经元在LAMP底物上基本不发生结合或延伸突起。所有细胞群体在聚 - D - 赖氨酸和层粘连蛋白上的结合和形成神经突的情况相同。目前的结果提供了直接证据,表明LAMP在发育过程中可特异性促进与中枢神经系统中特定神经元的相互作用。这些数据支持这样一种概念,即哺乳动物大脑功能相关区域中独特细胞黏附分子的模式化表达可调节回路形成。

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