Literature DB >> 7351042

Quantitative studies on plasmalemmal folds and caveolae of rabbit ventricular myocardial cells.

K R Levin, E Page.   

Abstract

Plasmalemmal folds and caveolae were investigated by qualitative and quantitative analysis of electron micrographs obtained by freeze fracture and transmission electron microscopy (TEM) of rabbit right ventricular papillary muscles whose mean sarcomere lengths ranged from 1.64 to 2.28 micron. In passively extended muscles, folds were observed at sarcomere lengths of 2.3 micron and could be shown by extrapolation to become completely extended at a maximum sarcomere length of 2.8 micron. It was concluded that the plasmalemma does not contribute to resting tension in the physiological range of sarcomere lengths. Caveolae are present in both the external plasmalemmal envelope and T-tubular plasmalemma. They show no preferential distribution with respect to underlying myofibrillar striations or membrane folds and are nearly devoid of membrane particles in freeze-fractured material. The surface density of caveolar necks (4.0/micron2 apparent plasmalemmal area) is only 16-20% of that reported for frog skeletal muscle. Caveolae augment plasmalemmal area by 21-32%, assuming two or three caveolae per neck, respectively. Caveolar membrane does not serve as a reservoir of membrane to be recruited into external plasmalemma, at least over the physiological range of sarcomere lengths. In heart muscle they do not account for the T-tubular access resistance, and their function in this tissue remains unknown.

Entities:  

Mesh:

Year:  1980        PMID: 7351042     DOI: 10.1161/01.res.46.2.244

Source DB:  PubMed          Journal:  Circ Res        ISSN: 0009-7330            Impact factor:   17.367


  31 in total

1.  Eisosome Ultrastructure and Evolution in Fungi, Microalgae, and Lichens.

Authors:  Jae-Hyeok Lee; John E Heuser; Robyn Roth; Ursula Goodenough
Journal:  Eukaryot Cell       Date:  2015-08-07

2.  Localization of sarcolemmal proteins to lipid rafts in the myocardium.

Authors:  Amy Cavalli; Mansoureh Eghbali; Tamara Y Minosyan; Enrico Stefani; Kenneth D Philipson
Journal:  Cell Calcium       Date:  2007-02-23       Impact factor: 6.817

3.  Superresolution imaging--caveolae, caveolins, mitochondria, and function in heart.

Authors:  W Jonathan Lederer
Journal:  Biophys J       Date:  2013-06-04       Impact factor: 4.033

4.  Organization of ryanodine receptors, transverse tubules, and sodium-calcium exchanger in rat myocytes.

Authors:  Isuru D Jayasinghe; Mark B Cannell; Christian Soeller
Journal:  Biophys J       Date:  2009-11-18       Impact factor: 4.033

Review 5.  Cardiac sodium channel mutations: why so many phenotypes?

Authors:  Man Liu; Kai-Chien Yang; Samuel C Dudley
Journal:  Nat Rev Cardiol       Date:  2014-06-24       Impact factor: 32.419

Review 6.  Different subcellular populations of L-type Ca2+ channels exhibit unique regulation and functional roles in cardiomyocytes.

Authors:  Jabe M Best; Timothy J Kamp
Journal:  J Mol Cell Cardiol       Date:  2011-08-23       Impact factor: 5.000

Review 7.  L-type calcium channel targeting and local signalling in cardiac myocytes.

Authors:  Robin M Shaw; Henry M Colecraft
Journal:  Cardiovasc Res       Date:  2013-02-14       Impact factor: 10.787

Review 8.  Cardiac T-Tubule Microanatomy and Function.

Authors:  TingTing Hong; Robin M Shaw
Journal:  Physiol Rev       Date:  2017-01       Impact factor: 37.312

Review 9.  BIN1 regulates dynamic t-tubule membrane.

Authors:  Ying Fu; TingTing Hong
Journal:  Biochim Biophys Acta       Date:  2015-11-11

10.  Mechanical properties of normal and mdx mouse sarcolemma: bearing on function of dystrophin.

Authors:  O F Hutter; F L Burton; D L Bovell
Journal:  J Muscle Res Cell Motil       Date:  1991-12       Impact factor: 2.698

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.