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利用扫描力显微镜鉴定完整细胞表面的小窝样结构。

Identification of caveolae-like structures on the surface of intact cells using scanning force microscopy.

作者信息

Lucius H, Friedrichson T, Kurzchalia T V, Lewin G R

机构信息

Department of Neuroscience, Max-Delbrück Institute for Molecular Medicine, D-13122 Berlin, Germany.

出版信息

J Membr Biol. 2003 Jul 15;194(2):97-108. doi: 10.1007/s00232-003-2029-5.

Abstract

Caveolae are small, functionally important membrane invaginations found on the surface of many different cell types. Using electron microscopy, caveolae can be unequivocally identified in cell membranes by virtue of their size and the presence of caveolin/VIP22 proteins in the caveolar coat. In this study we have applied for the first time scanning force microscopy (SFM), to visualize caveolae on the surface of living and fixed cells. By scanning the membranes of Chinese hamster ovary cells (CHO), using the tapping mode of the SFM in fluid, we could visualize small membrane pits on the cell membranes of living and fixed cells. Two populations of pits with mean diameters of around 100 nm and 200 nm were present. In addition, the location of many pits visualized with the SFM was coincident with membrane spots fluorescently labeled with a green fluorescent protein-caveolin-1 fusion protein. Scanning force microscopy on cells treated with methyl-beta-cyclodextrin, an agent that sequesters cholesterol and disrupts caveolae, abolished pits with a measured diameter of 100 nm but left pits of around 200 nm diameter intact. Thus, the smallest membrane pits measured with the SFM in CHO cells were indeed very likely to be identical to caveolae. These experiments show for the first time that SFM can be used to visualize caveolae in intact cells.

摘要

小窝是在许多不同细胞类型表面发现的微小且具有重要功能的膜内陷结构。借助电子显微镜,可依据小窝的大小以及小窝衣中窖蛋白/VIP22蛋白的存在情况,在细胞膜中明确识别出小窝。在本研究中,我们首次应用扫描力显微镜(SFM)来观察活细胞和固定细胞表面的小窝。通过在液体中利用SFM的轻敲模式扫描中国仓鼠卵巢细胞(CHO)的膜,我们能够观察到活细胞和固定细胞细胞膜上的小膜坑。存在平均直径约为100纳米和200纳米的两类膜坑。此外,用SFM观察到的许多膜坑的位置与用绿色荧光蛋白-窖蛋白-1融合蛋白进行荧光标记的膜斑相重合。对用甲基-β-环糊精处理的细胞进行扫描力显微镜观察,甲基-β-环糊精是一种螯合胆固醇并破坏小窝的试剂,它消除了直径为100纳米的膜坑,但直径约为200纳米的膜坑保持完整。因此,用SFM在CHO细胞中测量到的最小膜坑确实很可能与小窝相同。这些实验首次表明SFM可用于观察完整细胞中的小窝。

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