rdf:type |
|
lifeskim:mentions |
umls-concept:C0006675,
umls-concept:C0025251,
umls-concept:C0030685,
umls-concept:C0034693,
umls-concept:C0034721,
umls-concept:C0178719,
umls-concept:C0204727,
umls-concept:C0205409,
umls-concept:C0332281,
umls-concept:C0391871,
umls-concept:C0392747,
umls-concept:C0680255,
umls-concept:C0814999,
umls-concept:C1283071,
umls-concept:C1698986,
umls-concept:C1880022,
umls-concept:C1963578
|
pubmed:issue |
2
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pubmed:dateCreated |
1994-7-19
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pubmed:abstractText |
Membrane potential changes accompanying Ca2+ influx stimulated by release of Ca2+ from intracellular stores (store-regulated Ca2+ uptake) were monitored in BAPTA-loaded rat thymic lymphocytes using the fluorescent indicator bis(1,3-diethylthiobarbituric acid)trimethine oxonol. Depletion of [Ca2+]i stores by the application of thapsigargin, ionomycin or cyclopiazonic acid induced a depolarization which was (i) dependent upon BAPTA-loading, (ii) dependent upon extracellular Ca2+, (iii) independent of extracellular Na+ and (iv) abolished by 5 mM extracellular Ni2+. This depolarization was followed by a charybdotoxin-sensitive repolarization and subsequent hyperpolarization to values approximating the K+ equilibrium potential, consistent with secondary activation of a K+ conductance. These membrane potential changes temporally correlated with Ca2+ influx from the extracellular medium as measured fluorimetrically with indo-1. The divalent cation permeability sequence was investigated by monitoring the magnitude of the depolarization observed following the addition of 4 mM Ca2+, Mn2+, Ba2+ or Sr2+ to cells pretreated with doses of thapsigargin or ionomycin known to activate the store-regulated calcium uptake pathway. On the basis of these experiments, we conclude that the store-regulated Ca2+ uptake pathway has the following permeability sequence: Ca2+ > Mn2+ >> Ba2+, Sr2+ with Mn2+ displaying significant permeability relative to Ca2+. This pathway is distinguishable from other divalent cation uptake pathways reported in other cells types on the basis of its activation by thapsigargin and its high Mn2+ permeability.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/1,2-bis(2-aminophenoxy)ethane-N,N,N'...,
http://linkedlifedata.com/resource/pubmed/chemical/Barium,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Egtazic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Indoles,
http://linkedlifedata.com/resource/pubmed/chemical/Ionomycin,
http://linkedlifedata.com/resource/pubmed/chemical/Manganese,
http://linkedlifedata.com/resource/pubmed/chemical/Nickel,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Terpenes,
http://linkedlifedata.com/resource/pubmed/chemical/Thapsigargin,
http://linkedlifedata.com/resource/pubmed/chemical/cyclopiazonic acid
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0022-2631
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:volume |
137
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
159-68
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8006954-Animals,
pubmed-meshheading:8006954-Barium,
pubmed-meshheading:8006954-Calcium,
pubmed-meshheading:8006954-Cell Membrane,
pubmed-meshheading:8006954-Cell Membrane Permeability,
pubmed-meshheading:8006954-Cells, Cultured,
pubmed-meshheading:8006954-Egtazic Acid,
pubmed-meshheading:8006954-Indoles,
pubmed-meshheading:8006954-Ionomycin,
pubmed-meshheading:8006954-Lymphocytes,
pubmed-meshheading:8006954-Male,
pubmed-meshheading:8006954-Manganese,
pubmed-meshheading:8006954-Membrane Potentials,
pubmed-meshheading:8006954-Nickel,
pubmed-meshheading:8006954-Potassium Channels,
pubmed-meshheading:8006954-Rats,
pubmed-meshheading:8006954-Rats, Wistar,
pubmed-meshheading:8006954-Terpenes,
pubmed-meshheading:8006954-Thapsigargin,
pubmed-meshheading:8006954-Thymus Gland
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pubmed:year |
1994
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pubmed:articleTitle |
Isolation and characterization of membrane potential changes associated with release of calcium from intracellular stores in rat thymic lymphocytes.
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pubmed:affiliation |
Department of Physiology, Tulane University School of Medicine, New Orleans, Louisiana 70112.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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