ADP receptor P2Y12 is the capstone of the cross-talk between Ca

ADP NAADP P2 purinergic receptor (P2Y12 P2Y1) SERCA3 blood platelets

Journal

Research and practice in thrombosis and haemostasis
ISSN: 2475-0379
Titre abrégé: Res Pract Thromb Haemost
Pays: United States
ID NLM: 101703775

Informations de publication

Date de publication:
Jan 2023
Historique:
received: 14 06 2022
revised: 10 11 2022
accepted: 14 11 2022
entrez: 27 3 2023
pubmed: 28 3 2023
medline: 28 3 2023
Statut: epublish

Résumé

Blood platelet Ca The aim of this study was to identify which ADP P2 purinergic receptor (P2Y1 and/or P2Y12) is(are) involved in the amplification of platelet secretion dependent on the SERCA3-dependent Ca The study used the pharmacologic antagonists MRS2719 and AR-C69931MX, of the P2Y1 and P2Y12, respectively, as well as We found that in mouse platelets, pharmacological blockade or gene inactivation of P2Y12 but not of P2Y1 led to a marked inhibition of ADP secretion after platelet stimulation with low concentration of thrombin. Likewise, in human platelets, pharmacological inhibition of P2Y12 but not of P2Y1 alters amplification of thrombin-elicited secretion through SERCA2b stores mobilization. Finally, we show that early SERCA3 stores secretion of ADP is a dense granule secretion, based on parallel adenosine triphosphate and serotonin early secretion. Furthermore, early secretion involves a single granule, based on the amount of adenosine triphosphate released. Altogether, these results show that at low concentrations of thrombin, SERCA3- and SERCA2b-dependent Ca

Sections du résumé

Background UNASSIGNED
Blood platelet Ca
Objectives UNASSIGNED
The aim of this study was to identify which ADP P2 purinergic receptor (P2Y1 and/or P2Y12) is(are) involved in the amplification of platelet secretion dependent on the SERCA3-dependent Ca
Methods UNASSIGNED
The study used the pharmacologic antagonists MRS2719 and AR-C69931MX, of the P2Y1 and P2Y12, respectively, as well as
Results UNASSIGNED
We found that in mouse platelets, pharmacological blockade or gene inactivation of P2Y12 but not of P2Y1 led to a marked inhibition of ADP secretion after platelet stimulation with low concentration of thrombin. Likewise, in human platelets, pharmacological inhibition of P2Y12 but not of P2Y1 alters amplification of thrombin-elicited secretion through SERCA2b stores mobilization. Finally, we show that early SERCA3 stores secretion of ADP is a dense granule secretion, based on parallel adenosine triphosphate and serotonin early secretion. Furthermore, early secretion involves a single granule, based on the amount of adenosine triphosphate released.
Conclusion UNASSIGNED
Altogether, these results show that at low concentrations of thrombin, SERCA3- and SERCA2b-dependent Ca

Identifiants

pubmed: 36970741
doi: 10.1016/j.rpth.2022.100004
pii: S2475-0379(22)01100-1
pmc: PMC10031336
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100004

Informations de copyright

© 2022 The Author(s).

Références

Blood. 2016 Nov 24;128(21):2538-2549
pubmed: 27625359
Br J Haematol. 1997 Apr;97(1):192-203
pubmed: 9136965
J Biol Chem. 2004 Jun 4;279(23):24297-306
pubmed: 15028735
Circ Res. 2020 Sep 11;127(7):e166-e183
pubmed: 32588751
J Biol Chem. 1992 Jul 15;267(20):14483-9
pubmed: 1385815
Am J Physiol. 1982 Sep;243(3):R454-61
pubmed: 7114301
Platelets. 2005 May-Jun;16(3-4):133-50
pubmed: 16011958
Blood. 2016 Aug 25;128(8):1129-38
pubmed: 27301859
Biochem J. 1993 Apr 1;291 ( Pt 1):235-40
pubmed: 8385934
J Thromb Haemost. 2009 Jul;7(7):1057-66
pubmed: 19422456
J Biol Chem. 1997 Nov 28;272(48):30538-45
pubmed: 9374548
Biochim Biophys Acta. 2009 Feb;1793(2):223-30
pubmed: 19061922
Blood. 2007 Feb 15;109(4):1503-6
pubmed: 17032923
Blood. 2005 May 1;105(9):3552-60
pubmed: 15665114
Biochem Soc Trans. 2015 Jun;43(3):502-7
pubmed: 26009198
J Biol Chem. 1994 Jan 14;269(2):1410-6
pubmed: 8288608
Biochem J. 1996 Sep 1;318 ( Pt 2):689-99
pubmed: 8809064
Arterioscler Thromb Vasc Biol. 2016 Jun;36(6):1164-73
pubmed: 27079884
J Thromb Haemost. 2015 Jun;13 Suppl 1:S10-6
pubmed: 26149010
Adv Exp Med Biol. 2016;898:333-52
pubmed: 27161235
Annu Rev Pharmacol Toxicol. 2006;46:277-300
pubmed: 16402906
J Biol Chem. 2002 Jan 25;277(4):2965-72
pubmed: 11713259
Adv Exp Med Biol. 2017;993:139-157
pubmed: 28900913
Thromb Haemost. 2019 Mar;119(3):384-396
pubmed: 30650444
Handb Exp Pharmacol. 2012;(210):59-85
pubmed: 22918727
Biochem Pharmacol. 2008 Jun 1;75(11):2157-64
pubmed: 18439569
Biochem J. 1992 Aug 15;286 ( Pt 1):135-40
pubmed: 1387787
Purinergic Signal. 2011 Sep;7(3):293-303
pubmed: 21792575
Cell Signal. 2006 Mar;18(3):373-81
pubmed: 16095882
Nature. 2002 Aug 8;418(6898):605-11
pubmed: 12167852

Auteurs

Miao Feng (M)

HITh, UMR_S1176, INSERM, Université Paris-Saclay, Le Kremlin-Bicêtre, Paris, France.

Béatrice Hechler (B)

Université de Strasbourg, INSERM, Etablissement Français du Sang (EFS)-Grand Est, BPPS UMR_S 1255, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Strasbourg, France.

Frédéric Adam (F)

HITh, UMR_S1176, INSERM, Université Paris-Saclay, Le Kremlin-Bicêtre, Paris, France.

Christian Gachet (C)

Université de Strasbourg, INSERM, Etablissement Français du Sang (EFS)-Grand Est, BPPS UMR_S 1255, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Strasbourg, France.

Anita Eckly (A)

Université de Strasbourg, INSERM, Etablissement Français du Sang (EFS)-Grand Est, BPPS UMR_S 1255, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Strasbourg, France.

Alexandre Kauskot (A)

HITh, UMR_S1176, INSERM, Université Paris-Saclay, Le Kremlin-Bicêtre, Paris, France.

Cécile V Denis (CV)

HITh, UMR_S1176, INSERM, Université Paris-Saclay, Le Kremlin-Bicêtre, Paris, France.

Marijke Bryckaert (M)

HITh, UMR_S1176, INSERM, Université Paris-Saclay, Le Kremlin-Bicêtre, Paris, France.

Régis Bobe (R)

HITh, UMR_S1176, INSERM, Université Paris-Saclay, Le Kremlin-Bicêtre, Paris, France.

Jean-Philippe Rosa (JP)

HITh, UMR_S1176, INSERM, Université Paris-Saclay, Le Kremlin-Bicêtre, Paris, France.

Classifications MeSH