Molecular Proteomics and Signalling of Human Platelets in Health and Disease.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
13 Sep 2021
Historique:
received: 20 07 2021
revised: 31 08 2021
accepted: 02 09 2021
entrez: 28 9 2021
pubmed: 29 9 2021
medline: 21 10 2021
Statut: epublish

Résumé

Platelets are small anucleate blood cells that play vital roles in haemostasis and thrombosis, besides other physiological and pathophysiological processes. These roles are tightly regulated by a complex network of signalling pathways. Mass spectrometry-based proteomic techniques are contributing not only to the identification and quantification of new platelet proteins, but also reveal post-translational modifications of these molecules, such as acetylation, glycosylation and phosphorylation. Moreover, target proteomic analysis of platelets can provide molecular biomarkers for genetic aberrations with established or non-established links to platelet dysfunctions. In this report, we review 67 reports regarding platelet proteomic analysis and signalling on a molecular base. Collectively, these provide detailed insight into the: (i) technical developments and limitations of the assessment of platelet (sub)proteomes; (ii) molecular protein changes upon ageing of platelets; (iii) complexity of platelet signalling pathways and functions in response to collagen, rhodocytin, thrombin, thromboxane A

Identifiants

pubmed: 34576024
pii: ijms22189860
doi: 10.3390/ijms22189860
pmc: PMC8468031
pii:
doi:

Substances chimiques

Proteome 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Horizon 2020 Framework Programme
ID : TAPAS, TICARDIO
Organisme : Ministerium für Innovation, Wissenschaft und Forschung des Landes Nordrhein-Westfalen
ID : N/a
Organisme : Bundesministerium für Bildung und Forschung
ID : BMBF 01EO1503
Organisme : Deutsche Forschungsgemeinschaft
ID : ZA 639/4-1 and JU 2735/2-1
Organisme : Bundesministerium für Bildung und Forschung
ID : BMBF 01O1503
Organisme : Ministerio de Ciencia e Innovación
ID : PID2019-108727RB-100
Organisme : European Regional Development Fund
ID : ERDF

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Auteurs

Jingnan Huang (J)

Leibniz Institut für Analytische Wissenschaften-ISAS-e.V., 44139 Dortmund, Germany.
Department of Biochemistry, CARIM, Maastricht University, 6229 ER Maastricht, The Netherlands.
Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), Universidade de Santiago de Compostela, 15706 Santiago de Compostela, Spain.

Pengyu Zhang (P)

Leibniz Institut für Analytische Wissenschaften-ISAS-e.V., 44139 Dortmund, Germany.
Department of Biochemistry, CARIM, Maastricht University, 6229 ER Maastricht, The Netherlands.
Center for Thrombosis and Haemostasis, University Medical Center of the Johannes Gutenberg University Mainz, 55131 Mainz, Germany.

Fiorella A Solari (FA)

Leibniz Institut für Analytische Wissenschaften-ISAS-e.V., 44139 Dortmund, Germany.

Albert Sickmann (A)

Leibniz Institut für Analytische Wissenschaften-ISAS-e.V., 44139 Dortmund, Germany.
Medizinische Fakultät, Medizinische Proteom-Center, Ruhr-Universität Bochum, 44801 Bochum, Germany.
Department of Chemistry, College of Physical Sciences, University of Aberdeen, Aberdeen AB24 3FX, UK.

Angel Garcia (A)

Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), Universidade de Santiago de Compostela, 15706 Santiago de Compostela, Spain.

Kerstin Jurk (K)

Center for Thrombosis and Haemostasis, University Medical Center of the Johannes Gutenberg University Mainz, 55131 Mainz, Germany.

Johan W M Heemskerk (JWM)

Department of Biochemistry, CARIM, Maastricht University, 6229 ER Maastricht, The Netherlands.

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