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通过高压冷冻固定的假液泡与沃克癌肉瘤细胞中的泡状突起有关。

Pseudovacuoles--immobilized by high-pressure freezing--are associated with blebbing in walker carcinosarcoma cells.

作者信息

Vanhecke D, Bellmann R, Baum O, Graber W, Eggli P, Keller H, Studer D

机构信息

Department for Topographic Anatomy and Neuroanatomy, Institute of Anatomy, University of Bern, Switzerland.

出版信息

J Microsc. 2008 May;230(Pt 2):253-62. doi: 10.1111/j.1365-2818.2008.01982.x.

Abstract

By applying high pressure freezing and freeze-substitution, we observed large inclusions of homogeneous appearance in the front of locomoting Walker carcinosarcoma cells that have not been described earlier. Live cell imaging revealed that these inclusions were poor in lipids and nucleic acids but had a high lysine (and hence protein) content. Usually one such structure 2-5 mum in size was present at the front of motile Walker cells, predominantly in the immediate vicinity of newly forming blebs. By correlating the lysine-rich areas in fixed and embedded cells with electron microscopic pictures, inclusions could be assigned to confined, faintly stained cytoplasmic areas that lacked a surrounding membrane; they were therefore called pseudovacuoles. After high-pressure freezing and freeze substitution, pseudovacuoles appeared to be filled with 20 nm large electron-transparent patches surrounded by 12 and 15 nm large particles. The heat shock protein Hsp90 was identified by peptide sequencing as a major fluorescent band on SDS-PAGE of lysine-labelled Walker cell extracts. By immunofluorescence, Hsp90 was found to be enriched in pseudovacuoles. Colocalization of the lysine with a potassium-specific dye in living cells revealed that pseudovacuoles act as K+ stores in the vicinity of forming blebs. We propose that pseudovacuoles might support blebbing by locally regulating the intracellular hydrostatic pressure.

摘要

通过应用高压冷冻和冷冻置换技术,我们在游走的沃克癌肉瘤细胞前端观察到了外观均一的大内含物,这在之前尚未有过描述。活细胞成像显示,这些内含物的脂质和核酸含量较低,但赖氨酸(因而蛋白质)含量较高。通常在运动的沃克细胞前端会出现一个这样大小为2 - 5微米的结构,主要位于新形成的泡附近。通过将固定和包埋细胞中富含赖氨酸的区域与电子显微镜图像相关联,内含物可被归为局限的、染色较浅的无包膜细胞质区域;因此它们被称为假液泡。经过高压冷冻和冷冻置换后,假液泡似乎充满了由12纳米和15纳米大小的颗粒包围的20纳米大的电子透明斑块。通过肽测序鉴定,热休克蛋白Hsp90是赖氨酸标记的沃克细胞提取物SDS - PAGE上的主要荧光条带。通过免疫荧光发现,Hsp90在假液泡中富集。赖氨酸与活细胞中钾特异性染料的共定位显示,假液泡在形成泡的附近充当钾离子储存库。我们提出,假液泡可能通过局部调节细胞内静水压力来支持泡的形成。

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