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刷状缘运动性的重新评估:钙诱导核心细丝溶解和微绒毛囊泡化。

Reevaluation of brush border motility: calcium induces core filament solution and microvillar vesiculation.

作者信息

Burgess D R, Prum B E

出版信息

J Cell Biol. 1982 Jul;94(1):97-107. doi: 10.1083/jcb.94.1.97.

Abstract

The report that microvillar cores of isolated, demembranated brush borders retract into the terminal web in the presence of Ca(++) and ATP has been widely cited as an example of Ca(++)-regulated nonmuscle cell motility. Because of recent findings that microvillar core actin filaments are cross-linked by villin which, in the presence of micromolar Ca(++), fragments actin filaments, we used the techniques of video enhanced differential interference contrast, immunofluorescence, and phase contrast microscopy and thin-section electron microscopy (EM) to reexamine the question of contraction of isolated intestinal cell brush borders. Analysis of video enhanced light microscopic images of Triton- demembranated brush borders treated with a buffered Ca(++) solution shows the cores disintegrating with the terminal web remaining intact; membranated brush borders show the microvilli to vesiculate with Ca(++). Using Ca(++)/EGTA buffers, it is found that micromolar free Ca(++) causes core filament dissolution in membranated or demembranated brush borders, Ca(++) causes microvillar core solation followed by complete vesiculation of the microvillar membrane. The lengths of microvilli cores and rootlets were measured in thin sections of membranated and demembranated controls, in Ca(++)-, Ca(++) + ATP-, and in ATP-treated brush borders. Results of these measurements show that Ca(++) alone causes the complete solation of the microvillar cores, yet the rootlets in the terminal web region remain of normal length. These results show that microvilli do not retract into the terminal web in response to Ca(++) and ATP but rather that the microvillar cores disintegrate. NBD-phallicidin localization of actin and fluorescent antibodies to myosin reveal a circumferential band of actin and myosin in mildly permeabilized cells in the region of the junctional complex. The presence of these contractile proteins in this region, where other studies have shown a circumferential band of thin filaments, is consistent with the hypothesis that brush borders may be motile through the circumferential constriction of this "contractile ring," and is also consistent with the observations that ATP-treated brush borders become cup shaped as if there had been a circumferential constriction.

摘要

有报告称,分离的、去膜的刷状缘微绒毛核心在钙离子(Ca(++))和三磷酸腺苷(ATP)存在的情况下会缩回到终末网,这一报告被广泛引述为钙离子调节的非肌肉细胞运动性的一个例子。由于最近发现微绒毛核心肌动蛋白丝由绒毛蛋白交联,而在微摩尔浓度的钙离子存在时,绒毛蛋白会使肌动蛋白丝断裂,我们使用视频增强微分干涉相差、免疫荧光、相差显微镜和超薄切片电子显微镜(EM)技术,重新审视分离的肠细胞刷状缘收缩的问题。对用缓冲钙离子溶液处理的经曲拉通去膜的刷状缘的视频增强光学显微镜图像分析表明,微绒毛核心解体,而终末网保持完整;有膜的刷状缘显示微绒毛在钙离子作用下形成小泡。使用钙离子/乙二醇双乙胺四乙酸(EGTA)缓冲液发现,微摩尔浓度的游离钙离子会导致有膜或去膜刷状缘中的核心丝溶解,钙离子会导致微绒毛核心溶解,随后微绒毛膜完全形成小泡。在有膜和去膜对照的超薄切片中,以及在钙离子、钙离子+ATP和ATP处理的刷状缘中,测量了微绒毛核心和根的长度。这些测量结果表明,仅钙离子就能导致微绒毛核心完全溶解,但终末网区域的根仍保持正常长度。这些结果表明,微绒毛不会因钙离子和ATP而缩回到终末网,而是微绒毛核心解体。肌动蛋白的NBD - 鬼笔环肽定位和针对肌球蛋白的荧光抗体显示,在连接复合体区域轻度通透的细胞中,肌动蛋白和肌球蛋白形成一个周向带。在该区域存在这些收缩蛋白,其他研究在该区域显示有细肌丝周向带,这与刷状缘可能通过该“收缩环”的周向收缩而运动的假设一致,也与ATP处理的刷状缘变成杯状(就好像有周向收缩)的观察结果一致。

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