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PMID: 6833396 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Pattern and time course of rhodamine-actin incorporation in cardiac myocytes.

The Journal of cell biology ·Vol. 96 ·No. 4 ·1983-04-00 ·Pages 1164-7

Glacy SD

Abstract

Microinjection of skeletal actin labeled with rhodamine into cultured cardiac myocytes was followed by rapid incorporation of fluorescence into myofibrils of the cells. Myocytes examined as shortly as 5 min postinjection displayed fluorescent bands corresponding to the sarcomeres. By 10 min, distinct alternating wide and narrow bands of fluorescence were observed. The wide bands appeared to correspond to the full breadth of the I-bands, whereas the narrow bands of fluorescence corresponded to the M-lines. This pattern of fluorescence remained essentially unchanged for at least 15 h postinjection. The myofibrils of cardiac myocytes were functional after rhodamine-actin incorporation as judged by their ability to contract. The results of this study suggest that cardiac myofibrils are morphologically stable structures which, nonetheless, exhibit extensive exchange of actin subunits.

MeSH Terms
Actins/metabolism Animals Cells, Cultured Chick Embryo Microinjections Microscopy, Fluorescence Myocardium/metabolism Myofibrils/metabolism Rhodamines/metabolism Xanthenes/metabolism
Chemicals
Actins Rhodamines Xanthenes
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Glacy S D
References (13)
13 references, click to expand
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Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
0021-9525
Published
1983-04-00
Pages
1164-7
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2112326
Subset
IM
Grants
NICHD NIH HHS · HD-07193 · United States
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