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血管平滑肌激活与收缩的超微结构特征

Ultrastructural aspects of activation and contraction of vascular smooth muscle.

作者信息

Somlyo A P, Somlyo A V

出版信息

Fed Proc. 1976 May 1;35(6):1288-93.

PMID:770202
Abstract

Ultrastructural studies of potential intracellular calcium storage sites and of the organization of contractile proteins in vascular smooth muscle are reviewed. The sarcoplasmic reticulum (SR) is a system of closed tubules present in every smooth muscle examined. The volume of the SR varies in different smooth muscles (from approximately 2.0 to 7.5% of cytoplasmic volume) and correlates with the ability of a given smooth muscle to contract in calcium-free media. The SR accumulates the divalent cation strontium and forms couplings with the surface membrane. Mitochondria are other potential sites of calcium accumulation in vascular smooth muscle, as indicated by the respiration supported accumulation of calcium (with a Km of approximately 17 muM) by isolated mitochondria and by the energy dependent accumulation of barium by mitochondria in situ. The presence of barium in mitochondrial granules in tissues contracted with barium and the presence of strontium and calcium in appropriately incubated preparations have been verified with electron probe microanalysis. Calcium has also been demonstrated in mitochondrial granules in frozen dried cardiac muscle sections and in cultured vascular smooth muscle cells. This technique appears suitable for eventual quantitation of mitochondrial calcium content in vascular and other smooth muscles. Thin (actin, 50-80 A), thick (myosin, approximately 155 A), and intermediate (approximately 100 A) filaments are present in suitably fixed vascular smooth muscle. In rabbit portal anterior mesenteric vein intermediate high voltage stereo electron microscopy shows the myosin filaments to be tapered and approximately 2.2 mum long: significantly longer than the myosin filaments in vertebrate striated muscle. Actin filaments insert on dense bodies. The ultrastructural findings are compatible with physiological evidence suggesting the contributions of intracellular organelles to the regulation of cytoplasmic free calcium levels and the operation of a sliding filament mechanism of contraction in vertebrate smooth muscle.

摘要

本文综述了血管平滑肌中潜在的细胞内钙储存位点及收缩蛋白组织的超微结构研究。肌浆网(SR)是在每一种所研究的平滑肌中都存在的封闭小管系统。SR的体积在不同的平滑肌中有所变化(占细胞质体积的约2.0%至7.5%),并且与特定平滑肌在无钙培养基中收缩的能力相关。SR积累二价阳离子锶,并与表面膜形成连接。线粒体是血管平滑肌中钙积累的其他潜在位点,这一点可由分离的线粒体对钙的呼吸支持性积累(Km约为17μM)以及原位线粒体对钡的能量依赖性积累表明。通过电子探针微分析已证实,在用钡收缩的组织的线粒体颗粒中存在钡,以及在适当孵育的制剂中存在锶和钙。在冷冻干燥的心肌切片和培养的血管平滑肌细胞的线粒体颗粒中也已证实有钙存在。这项技术似乎适用于最终对血管及其他平滑肌中线粒体钙含量进行定量。在适当固定的血管平滑肌中存在细(肌动蛋白,50 - 80埃)、粗(肌球蛋白,约155埃)和中间(约100埃)丝。在兔门静脉前肠系膜静脉中,中间高压立体电子显微镜显示肌球蛋白丝呈锥形,长约2.2μm:明显长于脊椎动物横纹肌中的肌球蛋白丝。肌动蛋白丝插入致密体中。这些超微结构发现与生理学证据相符,表明细胞内细胞器对细胞质游离钙水平的调节以及脊椎动物平滑肌中收缩的滑动丝机制的运作有贡献。

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