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PMID: 5430787 Published · ppublish English Journal Article

The toxicity of streptolysin O for beating mammalian heart cells in tissue culture.

The Journal of experimental medicine ·Vol. 131 ·No. 4 ·1970-04-01 ·Pages 745-63

Thompson A, Halbert SP, Smith U

Abstract

Pulsating mammalian myocardial cells were found to be highly susceptible in tissue culture to rapid destruction by streptolysin O. Cessation of beating occurred almost immediately, followed within minutes by multiple cell membrane bleb formation. Parallel with these changes, the cytoplasm became intensely granular and the nuclear membrane apparently thickened when viewed by phase microscopy. At the ultrastructural level, the cell membrane blebs were found to contain relatively small numbers of granular fragments. The endoplasmic reticulum of damaged heart cells was quite swollen, and its contents were considerably condensed. The myofibers were not strikingly altered, but cytoplasmic and mitochondria vacuoles were rather abundant. Cardiac endothelial, kidney epithelial, and fibroblast cells were also susceptible to lysis by this toxin, but the reactions occurred more slowly or bleb formation was less evident. An antiserotonin drug known to be protective against streptolysin-O in vivo (UML-491), did not protect against killing of cardiac cells at the tissue culture level. Serotonin could not be detected in the culture fluid after lysis of cardiac cells by streptolysin O.

MeSH Terms
Animals Culture Techniques Ergolines/pharmacology Heart/drug effects Kidney/drug effects Microscopy, Electron Myocardium/cytology Rabbits Rats Serotonin/analysis Serotonin Antagonists Streptolysins/toxicity
Chemicals
Ergolines Serotonin Antagonists Streptolysins Serotonin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Thompson A
Halbert S P
Smith U
References (23)
23 references, click to expand
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1970-04-01
Pages
745-63
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2138779
Subset
IM
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