Abstract:
:To clarify the physiological role of calcium-activated neutral protease (CANP) in human platelets, we loaded the platelets with a Ca2+ -sensitive fluorescent dye, fura-2, and measured the degree of aggregation, cytosolic calcium ion concentration [( Ca2+]i), and proteolysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). At physiological concentration of Ca2+ (1 mM) in the incubation medium, [Ca2+]i was below 0.5 microM and platelet aggregation was not shown. Ionomycin (0.15 microM) or collagen (50 micrograms/ml), but not ADP (10 microM), sharply enhanced the [Ca2+]i to near 1 microM and caused the aggregation. A calcium entry blocker, verapamil, completely abolished both the [Ca2+]i rise and the aggregation. NCO-700, a membrane permeable inhibitor against cysteine proteases (including CANP), dose-dependently blocked the aggregation but did not change the [Ca2+]i transient. SDS-PAGE revealed that filamin, talin, and 70 kDa protein were specifically degraded when platelets were aggregated by ionomycin or collagen and that the proteolysis was not observed when the aggregation was blocked by verapamil or NCO-700. These data provided evidence that Ca2+ entry exceeding 0.5 microM is essential, but not sufficient per se, and that activation of cysteine protease, most likely CANP, is involved in the platelet aggregation by collagen or calcium ionophore.
journal_name
Circ Resjournal_title
Circulation researchauthors
Toyo-oka T,Shin WS,Okai Y,Dan Y,Morita M,Iizuka M,Sugimoto Tdoi
10.1161/01.res.64.2.407subject
Has Abstractpub_date
1989-02-01 00:00:00pages
407-10issue
2eissn
0009-7330issn
1524-4571journal_volume
64pub_type
杂志文章abstract::Alpha1-adrenoceptor (alpha1-AR) stimulation increases sarcolemmal Na+-H+ exchanger (NHE) activity. The present study was designed to determine the role(s) of alpha1-AR subtype(s) in mediating this response. As an index of NHE activity, acid efflux rates (JHs) were determined in single rat ventricular myocytes loaded w...
journal_title:Circulation research
pub_type: 杂志文章
doi:10.1161/01.res.82.10.1078
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journal_title:Circulation research
pub_type: 杂志文章,评审
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journal_title:Circulation research
pub_type: 杂志文章
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更新日期:1997-10-01 00:00:00
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journal_title:Circulation research
pub_type: 杂志文章
doi:10.1161/01.res.86.10.1093
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pub_type: 杂志文章
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pub_type: 杂志文章
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journal_title:Circulation research
pub_type: 杂志文章
doi:10.1161/01.res.86.5.580
更新日期:2000-03-17 00:00:00
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更新日期:2007-02-02 00:00:00
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journal_title:Circulation research
pub_type: 杂志文章
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更新日期:1993-08-01 00:00:00
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journal_title:Circulation research
pub_type: 杂志文章
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更新日期:2002-07-26 00:00:00
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journal_title:Circulation research
pub_type: 杂志文章
doi:10.1161/CIRCRESAHA.109.200311
更新日期:2009-07-17 00:00:00
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pub_type: 杂志文章
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更新日期:2003-04-18 00:00:00
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journal_title:Circulation research
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更新日期:1997-02-01 00:00:00
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pub_type: 杂志文章,评审
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更新日期:2008-05-09 00:00:00
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journal_title:Circulation research
pub_type: 杂志文章
doi:10.1161/01.res.72.5.984
更新日期:1993-05-01 00:00:00
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pub_type: 杂志文章
doi:10.1161/01.res.77.6.1166
更新日期:1995-12-01 00:00:00
abstract:RATIONALE:Mitochondria, although required for cellular ATP production, are also known to have other important functions that may include modulating cellular responses to environmental stimuli. However, the mechanisms whereby mitochondria impact cellular phenotype are not yet clear. OBJECTIVE:To determine how mitochond...
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pub_type: 杂志文章
doi:10.1161/CIRCRESAHA.113.301319
更新日期:2013-09-13 00:00:00
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journal_title:Circulation research
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更新日期:2016-08-19 00:00:00
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更新日期:2006-06-23 00:00:00
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更新日期:2000-02-04 00:00:00
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更新日期:2013-06-07 00:00:00
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pub_type: 杂志文章
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更新日期:1991-03-01 00:00:00
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更新日期:1978-07-01 00:00:00
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更新日期:2003-06-27 00:00:00
abstract::We discuss the recent finding by Mizishima's group regarding the role of the autophagy-related conjugation system in mediating the closure of autophagosomes and its implication in the study of autophagy in mammalian cells. The study not only shows a novel function of the autophagy-related conjugation system but also i...
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pub_type: 杂志文章,评审
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更新日期:2017-02-17 00:00:00
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更新日期:2015-09-11 00:00:00
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更新日期:1987-05-01 00:00:00
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更新日期:1982-07-01 00:00:00
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更新日期:1981-08-01 00:00:00