Severino Valeria, Farina Annarita, Colucci-D'Amato Luca, Reccia Mafalda Giovanna, Volpicelli Floriana, Parente Augusto, Chambery Angela
Department of Environmental, Biological and Pharmaceutical Sciences and Technologies, Second University of Naples, I-81100 Caserta, Italy.
Biochim Biophys Acta. 2013 Nov;1834(11):2385-95. doi: 10.1016/j.bbapap.2012.12.005. Epub 2012 Dec 12.
Neural stem cell proliferation and differentiation play a crucial role in the formation and wiring of neuronal connections forming neuronal circuits. During neural tissues development, a large diversity of neuronal phenotypes is produced from neural precursor cells. In recent years, the cellular and molecular mechanisms by which specific types of neurons are generated have been explored with the aim to elucidate the complex events leading to the generation of different phenotypes via distinctive developmental programs that control self-renewal, differentiation, and plasticity. The extracellular environment is thought to provide instructive influences that actively induce the production of specific neuronal phenotypes. In this work, the secretome profiling of differentiated neural mes-c-myc A1 (A1) cell line endowed with stem cell properties was analyzed by applying a shotgun LC-MS/MS approach. The results provide a list of secreted molecules with potential relevance for the functional and biological features characterizing the A1 neuronal phenotype. Proteins involved in biological processes closely related to nervous system development including neurites growth, differentiation of neurons and axonogenesis were identified. Among them, proteins belonging to extracellular matrix and cell-adhesion complexes as well as soluble factors with well established neurotrophic properties were detected. The presented work provides the basis to clarify the complex extracellular protein networks implicated in neuronal differentiation and in the acquisition of the neuronal phenotype. This article is part of a Special Issue entitled: An Updated Secretome.
神经干细胞的增殖和分化在神经元连接的形成及神经回路的构建中起着关键作用。在神经组织发育过程中,神经前体细胞可产生多种多样的神经元表型。近年来,人们探索了特定类型神经元产生的细胞和分子机制,旨在阐明通过控制自我更新、分化和可塑性的独特发育程序导致不同表型产生的复杂事件。细胞外环境被认为提供了具有指导作用的影响,可积极诱导特定神经元表型的产生。在这项工作中,通过应用鸟枪法液相色谱-串联质谱(LC-MS/MS)方法分析了具有干细胞特性的分化神经mes-c-myc A1(A1)细胞系的分泌蛋白质组。结果提供了一份与表征A1神经元表型的功能和生物学特征潜在相关的分泌分子清单。鉴定出了参与与神经系统发育密切相关的生物学过程的蛋白质,包括神经突生长、神经元分化和轴突形成。其中,检测到了属于细胞外基质和细胞粘附复合物的蛋白质以及具有公认神经营养特性的可溶性因子。所呈现的工作为阐明与神经元分化和神经元表型获得相关的复杂细胞外蛋白质网络提供了基础。本文是名为:更新后的分泌蛋白质组的特刊的一部分。