Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1998-3-5
|
pubmed:abstractText |
By voltage clamp technique and intracellular calcium measurements, we recorded in prawn oocytes simultaneous [Ca2+]i and ionic current changes stimulated by external Mg2+. The [Ca2+]i response consists of an oscillation period followed by a second state of sustained [Ca2+]i level. The oscillation period successively comprises a first [Ca2+]i peak, a series of [Ca2+]i transients, and a [Ca2+]i oscillatory plateau respectively concurrent with an initial transient outward K+Ca current, an inward Na+Ca current, and a final K+Ca outward current. By using inhibitor (heparin) or sensitizers (thimerosal or caffeine) of calcium release ER channels, and caged InsP3, we established that InsP3 is the sole second messenger releasing Ca2+ from intracellular stores. By sequential substitutions and reapplications of external Ca2+, and using econazole (50 microM), a Ca2+ influx inhibitor, we documented Ca2+ influx during the [Ca2+]i oscillatory plateau. The intracellular Ca2+ store was depleted with thapsigargin (75-350 nM) in Ca2+-free ASW. Reapplication of external Ca2+ evoked a rise in [Ca2+]i, indicating a store-dependent capacitative Ca2+ influx, correlated with a K+Ca outward current increase. No measurable Ca2+ release-activated Ca2+ current (Icrac) could be detected, but was indirectly demonstrated using the sensitivity of the K+Ca channels to [Ca2+]i. We propose that the involvement of external Ca2+, in the physiological [Ca2+]i response of prawn oocytes to external Mg2+, consists of a store-dependent capacitative Ca2+ influx.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Caffeine,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Heparin,
http://linkedlifedata.com/resource/pubmed/chemical/Inositol 1,4,5-Trisphosphate,
http://linkedlifedata.com/resource/pubmed/chemical/Magnesium,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Thapsigargin,
http://linkedlifedata.com/resource/pubmed/chemical/Thimerosal,
http://linkedlifedata.com/resource/pubmed/chemical/inositol 1,4,5-trisphosphate...
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0012-1606
|
pubmed:author | |
pubmed:copyrightInfo |
Copyright 1998 Academic Press.
|
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
193
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
225-38
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:9473326-Animals,
pubmed-meshheading:9473326-Caffeine,
pubmed-meshheading:9473326-Calcium,
pubmed-meshheading:9473326-Calcium Channels,
pubmed-meshheading:9473326-Cell Membrane,
pubmed-meshheading:9473326-Decapoda (Crustacea),
pubmed-meshheading:9473326-Female,
pubmed-meshheading:9473326-Heparin,
pubmed-meshheading:9473326-Inositol 1,4,5-Trisphosphate,
pubmed-meshheading:9473326-Intracellular Fluid,
pubmed-meshheading:9473326-Magnesium,
pubmed-meshheading:9473326-Microinjections,
pubmed-meshheading:9473326-Oocytes,
pubmed-meshheading:9473326-Patch-Clamp Techniques,
pubmed-meshheading:9473326-Photolysis,
pubmed-meshheading:9473326-Potassium Channels,
pubmed-meshheading:9473326-Thapsigargin,
pubmed-meshheading:9473326-Thimerosal
|
pubmed:year |
1998
|
pubmed:articleTitle |
Depletion of intracellular Ca2+ stores, mediated by Mg2+-stimulated InsP3 liberation or thapsigargin, induces a capacitative Ca2+ influx in prawn oocytes.
|
pubmed:affiliation |
Observatoire Océanographique et de Biologie marine de Roscoff, UPR CNRS 9042, France. hgoudeau@sbr.sb-roscoff.fr
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|