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Group VIB Calcium-Independent Phospholipase A(2) (iPLA(2)γ) Regulates Platelet Activation, Hemostasis and Thrombosis in Mice
In platelets, group IVA cytosolic phospholipase A(2) (cPLA(2)α) has been implicated as a key regulator in the hydrolysis of platelet membrane phospholipids, leading to pro-thrombotic thromboxane A(2) and anti-thrombotic 12-(S)-hydroxyeicosatetranoic acid production. However, studies using cPLA(2)α-d...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196902/ https://www.ncbi.nlm.nih.gov/pubmed/25313821 http://dx.doi.org/10.1371/journal.pone.0109409 |
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author | Yoda, Emiko Rai, Kohmi Ogawa, Mai Takakura, Yuki Kuwata, Hiroshi Suzuki, Hidenori Nakatani, Yoshihito Murakami, Makoto Hara, Shuntaro |
author_facet | Yoda, Emiko Rai, Kohmi Ogawa, Mai Takakura, Yuki Kuwata, Hiroshi Suzuki, Hidenori Nakatani, Yoshihito Murakami, Makoto Hara, Shuntaro |
author_sort | Yoda, Emiko |
collection | PubMed |
description | In platelets, group IVA cytosolic phospholipase A(2) (cPLA(2)α) has been implicated as a key regulator in the hydrolysis of platelet membrane phospholipids, leading to pro-thrombotic thromboxane A(2) and anti-thrombotic 12-(S)-hydroxyeicosatetranoic acid production. However, studies using cPLA(2)α-deficient mice have indicated that other PLA(2)(s) may also be involved in the hydrolysis of platelet glycerophospholipids. In this study, we found that group VIB Ca(2+)-independent PLA(2) (iPLA(2)γ)-deficient platelets showed decreases in adenosine diphosphate (ADP)-dependent aggregation and ADP- or collagen-dependent thromboxane A(2) production. Electrospray ionization mass spectrometry analysis of platelet phospholipids revealed that fatty acyl compositions of ethanolamine plasmalogen and phosphatidylglycerol were altered in platelets from iPLA(2)γ-null mice. Furthermore, mice lacking iPLA(2)γ displayed prolonged bleeding times and were protected against pulmonary thromboembolism. These results suggest that iPLA(2)γ is an additional, long-sought-after PLA(2) that hydrolyzes platelet membranes and facilitates platelet aggregation in response to ADP. |
format | Online Article Text |
id | pubmed-4196902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41969022014-10-16 Group VIB Calcium-Independent Phospholipase A(2) (iPLA(2)γ) Regulates Platelet Activation, Hemostasis and Thrombosis in Mice Yoda, Emiko Rai, Kohmi Ogawa, Mai Takakura, Yuki Kuwata, Hiroshi Suzuki, Hidenori Nakatani, Yoshihito Murakami, Makoto Hara, Shuntaro PLoS One Research Article In platelets, group IVA cytosolic phospholipase A(2) (cPLA(2)α) has been implicated as a key regulator in the hydrolysis of platelet membrane phospholipids, leading to pro-thrombotic thromboxane A(2) and anti-thrombotic 12-(S)-hydroxyeicosatetranoic acid production. However, studies using cPLA(2)α-deficient mice have indicated that other PLA(2)(s) may also be involved in the hydrolysis of platelet glycerophospholipids. In this study, we found that group VIB Ca(2+)-independent PLA(2) (iPLA(2)γ)-deficient platelets showed decreases in adenosine diphosphate (ADP)-dependent aggregation and ADP- or collagen-dependent thromboxane A(2) production. Electrospray ionization mass spectrometry analysis of platelet phospholipids revealed that fatty acyl compositions of ethanolamine plasmalogen and phosphatidylglycerol were altered in platelets from iPLA(2)γ-null mice. Furthermore, mice lacking iPLA(2)γ displayed prolonged bleeding times and were protected against pulmonary thromboembolism. These results suggest that iPLA(2)γ is an additional, long-sought-after PLA(2) that hydrolyzes platelet membranes and facilitates platelet aggregation in response to ADP. Public Library of Science 2014-10-14 /pmc/articles/PMC4196902/ /pubmed/25313821 http://dx.doi.org/10.1371/journal.pone.0109409 Text en © 2014 Yoda et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Yoda, Emiko Rai, Kohmi Ogawa, Mai Takakura, Yuki Kuwata, Hiroshi Suzuki, Hidenori Nakatani, Yoshihito Murakami, Makoto Hara, Shuntaro Group VIB Calcium-Independent Phospholipase A(2) (iPLA(2)γ) Regulates Platelet Activation, Hemostasis and Thrombosis in Mice |
title | Group VIB Calcium-Independent Phospholipase A(2) (iPLA(2)γ) Regulates Platelet Activation, Hemostasis and Thrombosis in Mice |
title_full | Group VIB Calcium-Independent Phospholipase A(2) (iPLA(2)γ) Regulates Platelet Activation, Hemostasis and Thrombosis in Mice |
title_fullStr | Group VIB Calcium-Independent Phospholipase A(2) (iPLA(2)γ) Regulates Platelet Activation, Hemostasis and Thrombosis in Mice |
title_full_unstemmed | Group VIB Calcium-Independent Phospholipase A(2) (iPLA(2)γ) Regulates Platelet Activation, Hemostasis and Thrombosis in Mice |
title_short | Group VIB Calcium-Independent Phospholipase A(2) (iPLA(2)γ) Regulates Platelet Activation, Hemostasis and Thrombosis in Mice |
title_sort | group vib calcium-independent phospholipase a(2) (ipla(2)γ) regulates platelet activation, hemostasis and thrombosis in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196902/ https://www.ncbi.nlm.nih.gov/pubmed/25313821 http://dx.doi.org/10.1371/journal.pone.0109409 |
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