Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1991-2-14
pubmed:abstractText
Inositol-polyphosphate-induced Ca2+ mobilization was investigated in saponin-permeabilized SH-SY5Y human neuroblastoma cells. Ins(1,4,5)P3 induced a dose-related release from intracellular Ca2+ stores with an EC50 (concn. giving half-maximal effect) of 0.1 microM and a maximal release of 70%. Ins(1,3,4)P3, DL-Ins(1,4,5,6)P4 and Ins(1,3,4,5,6)P5 did not evoke Ca2+ mobilization in these cells when used at concentrations up to 10 microM. However, Ins(1,3,4,5)P4 was found to release Ca2+ in a dose-related manner, but the response was dependent on the source of Ins(1,3,4,5)P4 used. When commercially available D-Ins(1,3,4,5)P4 was used, the EC50 and maximal response values were 1 microM and 50% respectively, compared with values for chemically synthesized DL-Ins(1,3,4,5)P4 of 2 microM and 25%. The enhanced maximal response of commercial D-Ins(1,3,4,5)P4 was decreased by pretreatment with rat brain crude Ins(1,4,5)P3 3-kinase and was therefore concluded to be indicative of initial Ins(1,4,5)P3 contamination of the Ins(1,3,4,5)P4 preparation. When metabolism of DL-Ins(1,3,4,5)P4 (10 microM) in these cells at 25 degrees C was investigated by h.p.l.c., substantial amounts of Ins(1,4,5)P3 (0.2 microM) and Ins(1,3,4)P3 (0.8 microM) were found to be produced within 3 min. Analysis of DL-Ins(1,3,4,5)P4 incubation with cells at 4 degrees C, however, indicated that metabolism had been arrested ([3H]Ins(1,4,5)P3 detection limits were estimated to be approx. 0.01 microM). When chemically synthesized DL-Ins(1,3,4,5)P4 and incubation conditions of low temperature were used, the Ca2(+)-releasing properties of this compound were established to be 1 microM and 19% for the EC50 and maximal response values respectively. The results obtained strongly suggest that Ins(1,3,4,5)P4 alone has the ability to release intracellular Ca2+. However, in the presence of sub-maximal concentrations of Ins(1,4,5)P3, Ca2+ release appears to be synergistic with Ins(1,3,4,5)P4, but at supramaximal concentrations not even additive effects are observed.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2163607, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2446148, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2469162, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2538711, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2546303, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2547768, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2548474, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2550275, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2550775, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2555352, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2667466, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2786415, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2818578, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2847317, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2906139, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2930510, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-2981051, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-3257739, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-3263119, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-3304132, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-3342011, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-3372512, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-3421904, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-3496245, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-3496884, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-3501290, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-3827851, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-3827881, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-3945308, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-4084229, http://linkedlifedata.com/resource/pubmed/commentcorrection/2176465-6236219
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0264-6021
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
272
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
519-24
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1990
pubmed:articleTitle
Inositol 1,3,4,5-tetrakisphosphate-induced release of intracellular Ca2+ in SH-SY5Y neuroblastoma cells.
pubmed:affiliation
Department of Pharmacology, University of Leicester, U.K.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't