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PMID: 6807344 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Calcium does not mediate the shape change that follows ATP depletion in human erythrocytes.

Biochimica et biophysica acta ·Vol. 687 ·No. 2 ·1982-05-07 ·Pages 321-8

Ferrell JE, Huestis WH

Abstract

Crenation, the shape change that follows ATP depletion in human erythrocytes, also follows ionphore-mediated Ca2+-loading. Experiments designed to test whether Ca2+ mediates metabolic crenation showed that: (1) an influx of extracellular Ca2+ is not required for metabolic crenation; (2) metabolic crenation is accompanied by a 70% increase in 86Rb+ permeability, a change much smaller than the increase expected if crenating concentrations of Ca2+ were released from bound intracellular pools; (3) A23187 plus EGTA, a treatment that depletes intracellular Ca2+ and stops Ca2+ crenation, does not affect metabolic crenation; (4) calmodulin inhibitors do not slow metabolic crenation. We conclude that Ca2+ does not mediate metabolic crenation. Albumin washes reverse Ca2+ crenation and metabolic crenation involve the accumulation of some amphiphilic species (e.g., lysolipid or diacylglycerol) in the cell membrane outer monolayer, and that ATP depletion induces a second crenating process which might be a reorganization of the cytoskeleton.

MeSH Terms
Adenosine Triphosphate/blood Calcimycin/pharmacology Calcium/blood,pharmacology Egtazic Acid/pharmacology Erythrocytes/drug effects,ultrastructure Humans Kinetics
Chemicals
Calcimycin Egtazic Acid Adenosine Triphosphate Calcium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ferrell J E
Huestis W H
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
1982-05-07
Pages
321-8
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
Grants
NHLBI NIH HHS · HL00258 · United States
NHLBI NIH HHS · HL23787 · United States
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