肾成纤维细胞培养。

C Grupp, G A Müller
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引用次数: 31

摘要

肾间质细胞不是一个均匀的细胞群,而是由不同类型的细胞组成,如成纤维细胞、树突状细胞或淋巴细胞样细胞。成纤维细胞是最丰富的间质细胞类型。它们被认为是细胞外基质生成和降解最重要的细胞,被认为在肾间质纤维化中起关键作用,而肾间质纤维化与排泄肾功能下降直接相关。肾成纤维细胞也具有内分泌活性:皮质成纤维细胞被认为可以合成促红细胞生成素,髓内成纤维细胞参与调节水和电解质稳态。对培养细胞的研究是进一步阐明成纤维细胞功能的有力工具。已经报道了分离成纤维细胞的不同技术,包括从切碎的组织外生物中培养成纤维细胞和通过各种方法选择性去除污染的上皮细胞。在培养成纤维细胞时必须考虑几个方面。成纤维细胞在培养中表现出不同的形态和生化特征,这取决于它们的起源位置、分化状态和培养条件。因此,在与其他细胞类型的混合培养中,仅通过形态学标准对其进行鉴定是至关重要的。不幸的是,对于所有成纤维细胞,仍然没有一个组成表达的特异性标记。由于肌成纤维细胞的形成被认为是肾间质纤维化的关键事件,因此成纤维细胞向肌成纤维细胞的转化引起了人们的特别关注。对培养成纤维细胞的研究为研究影响这种转化的因素和调节细胞外基质的产生和降解提供了有效的工具。此外,该技术可用于进一步表征培养成纤维细胞的内分泌活性。更好地了解成纤维细胞的生物学对于制定治疗肾小管间质纤维化的治疗策略至关重要,肾小管间质纤维化在病理上相当于进行性肾衰竭。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Renal fibroblast culture.

The interstitial cells in the kidney are not a homogeneous cell population but consist of different cell types like fibroblasts, dendritic cells or lymphocyte-like cells. Fibroblasts are the most abundant interstitial cell type. They are regarded as the most important cells for the production and degradation of extracellular matrix and are assumed to play a pivotal role in renal interstitial fibrosis, which correlates directly with the decrease in excretory renal function. Renal fibroblasts also have endocrine activity: cortical fibroblasts are supposed to synthesize erythropoeitin, and inner medullary fibroblasts are involved in the regulation of water and electrolyte homeostasis. A powerful tool for the further elucidation of fibroblast function are studies on cultured cells. Different techniques for the isolation of fibroblasts have been reported, including the cultivation of fibroblasts from outgrowths of minced tissue and the selective removal of contaminating epithelial cells by various methods. Several aspects have to be considered while culturing fibroblasts. Fibroblasts in culture exhibit distinct morphologic and biochemical features depending on their site of origin, state of differentiation and culture conditions. Their identification in culture exclusively by morphological criteria is therefore critical especially in mixed cultures with other cell types. Unfortunately, a constitutively expressed, specific marker for all fibroblasts is still not available. Since myofibroblast formation is considered as a key event in renal interstitial fibrosis, the transformation of fibroblasts to myofibroblasts is of special interest. Studies on cultured fibroblasts provide an effective tool to examine factors that affect this transformation and regulate the production and degradation of extracellular matrix. In addition, this technique can be used for further characterization of the endocrine activity of cultured fibroblasts. A better understanding of the biology of fibroblasts is essential to develop therapeutic strategies for the treatment of renal tubulointerstitial fibrosis, the pathologic equivalent of progressive renal failure.

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