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系膜细胞培养

Mesangial cell cultures.

作者信息

Menè P

机构信息

Division of Nephrology, Department of Clinical Sciences, University of Rome La Sapienza, Rome, Italy.

出版信息

J Nephrol. 2001 May-Jun;14(3):198-203.

Abstract

Cell culture of glomerular mesangial cells (MC) has been available to most renal research laboratories since the early 80s. Key to a large number of studies on the biochemistry and molecular biology of the glomerulus, MC in culture have extensive analogies with this in vivo rather undifferentiated intercapillary cell population. They proliferate in response to mitogens and growth factors, can be growth-arrested by withdrawal of serum or 3D culture in collagen gels, synthesize an extracellular matrix that includes interstitial collagens, and display most markers of mesangial origin, including a functional contractile apparatus. As proliferation and matrix synthesis/degradation in vitro are regulated by cytokines and growth factors, cultured cells are an ideal tool for studying pathophysiological events such as mesangial expansion, scarring, and glomerulosclerosis. Current techniques for MC isolation and culture are reviewed, with several methodological issues relevant to the characterization, propagation and long-term maintenance of functional clones.

摘要

自20世纪80年代初以来,大多数肾脏研究实验室都能够进行肾小球系膜细胞(MC)的细胞培养。作为大量关于肾小球生物化学和分子生物学研究的关键,培养中的MC与体内这种相当未分化的毛细血管间细胞群体有广泛的相似之处。它们对有丝分裂原和生长因子有反应而增殖,可通过血清撤离或在胶原凝胶中进行三维培养使其生长停滞,合成包括间质胶原在内的细胞外基质,并显示出系膜起源的大多数标志物,包括功能性收缩装置。由于体外的增殖和基质合成/降解受细胞因子和生长因子调节,培养的细胞是研究诸如系膜扩张、瘢痕形成和肾小球硬化等病理生理事件的理想工具。本文综述了目前MC分离和培养的技术,并讨论了与功能性克隆的表征、增殖和长期维持相关的几个方法学问题。

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