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靶源性基质细胞衍生因子通过 α3β1 整合素组织小脑突触形成。

Target-derived matricryptins organize cerebellar synapse formation through α3β1 integrins.

机构信息

Department of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, 23298, USA.

出版信息

Cell Rep. 2012 Aug 30;2(2):223-30. doi: 10.1016/j.celrep.2012.07.001. Epub 2012 Aug 9.

Abstract

Trans-synaptic organizing cues must be passed between synaptic partners for synapses to properly form. Much of our understanding of this process stems from studies at the neuromuscular junction, where target-derived growth factors, extracellular matrix (ECM) molecules, and matricryptins (proteolytically released fragments of ECM molecules) are all essential for the formation and maintenance of motor nerve terminals. While growth factors and ECM molecules also contribute to the formation of brain synapses, it remains unclear whether synaptic roles exist for matricryptins in the mammalian brain. We report that collagen XVIII and its matricryptin endostatin are generated by cerebellar Purkinje cells and are necessary for the organization of climbing fiber terminals in these neurons. Moreover, endostatin is sufficient to induce climbing fiber terminal formation in vitro by binding and signaling through α3β1 integrins. Taken together, these studies reveal roles for both matricryptins and integrins in the organization of brain synapses.

摘要

突触间的组织线索必须在突触伙伴之间传递,才能使突触正常形成。我们对这一过程的大部分理解都源于神经肌肉接头的研究,在那里,来自靶标的生长因子、细胞外基质 (ECM) 分子和基质细胞蛋白酶 (ECM 分子的蛋白水解片段) 对于运动神经末梢的形成和维持都是必不可少的。虽然生长因子和 ECM 分子也有助于脑突触的形成,但基质细胞蛋白酶在哺乳动物大脑中的突触作用是否存在仍不清楚。我们报告说,胶原 XVIII 及其基质细胞蛋白酶内皮抑素由小脑浦肯野细胞产生,对于这些神经元中攀爬纤维末梢的组织是必需的。此外,内皮抑素通过结合和通过α3β1 整联蛋白信号传导足以在体外诱导攀爬纤维末梢的形成。总之,这些研究揭示了基质细胞蛋白酶和整联蛋白在脑突触组织中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9977/3432753/04b3cba51f17/nihms-395527-f0001.jpg

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