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肾细胞系MDCK和LLC-PK1中内质网的组织

Organization of the endoplasmic reticulum in renal cell lines MDCK and LLC-PK1.

作者信息

Bergeron M, Thiéry G, Lenoir F, Giocondi M C, Le Grimellec C

机构信息

Département de Physiologie, Faculté de Médecine, Université de Montréal, Québec, Canada.

出版信息

Cell Tissue Res. 1994 Aug;277(2):297-307. doi: 10.1007/BF00327777.

Abstract

The spatial organization of the endoplasmic reticulum has been studied in two renal cell lines, MDCK and LLC-PK1, which originate from the distal and proximal portions of the mammalian nephron, respectively, and which form a polarized epithelium when they reach confluence in tissue culture. The two renal cell lines, grown to confluence on either solid or permeable supports, were investigated by fluorescence microscopy, confocal microscopy, and transmission electron microscopy. Fluorescence labeling of the endoplasmic reticulum was achieved using the cationic fluorescent dye DIOC6 (3). In order to differentiate fluorescent labeling of the endoplasmic reticulum from that of the mitochondria, cells were also labeled with rhodamine 123. For electron microscopy, the spatial organization of the endoplasmic reticulum was examined in thick sections using the long-duration osmium impregnation technique or the ferrocyanide/osmium technique. In both cell lines, the endoplasmic reticulum formed an abundant tubular network of canaliculi that frequently abutted the basolateral domain of the plasma membrane and occasionally the apical membrane. Elements of the endoplasmic reticulum were also found in close proximity to mitochondria that, as in the nephron, formed branched structures. Canaliculi appeared circular or flattened and had an inner diameter of 10-70 nm for MDCK cells and 20-90 nm for LLC-PK1 cells. Such a three-dimensional organization might facilitate the translocation of defined lipid species between the endoplasmic reticulum and the plasma membrane, and between the endoplasmic reticulum and mitochondria.

摘要

在内质网的空间组织已经在两种肾细胞系,MDCK和LLC-PK1中进行了研究,它们分别起源于哺乳动物肾单位的远端和近端部分,并且当它们在组织培养中达到汇合时形成极化上皮。这两种肾细胞系在固体或可渗透支持物上生长至汇合后,通过荧光显微镜、共聚焦显微镜和透射电子显微镜进行研究。使用阳离子荧光染料DIOC6(3)实现内质网的荧光标记。为了将内质网的荧光标记与线粒体的荧光标记区分开来,细胞还用罗丹明123进行标记。对于电子显微镜,使用长时间锇浸渍技术或亚铁氰化物/锇技术在厚切片中检查内质网的空间组织。在这两种细胞系中,内质网形成了丰富的小管状网络,这些小管经常邻接质膜的基底外侧结构域,偶尔也邻接顶端膜。内质网的成分也被发现在靠近线粒体的位置,线粒体与肾单位中的情况一样,形成分支结构。小管呈圆形或扁平状,MDCK细胞的内径为10-70nm,LLC-PK1细胞的内径为20-90nm。这样的三维组织可能有助于特定脂质分子在内质网与质膜之间,以及内质网与线粒体之间的转运。

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