Literature DB >> 12909311

Microparticles in cardiovascular diseases.

Marja J VanWijk1, E VanBavel, A Sturk, R Nieuwland.   

Abstract

Microparticles are membrane vesicles released from many different cell types. There are two mechanisms that can result in their formation, cell activation and apoptosis. In these two mechanisms, different pathways are involved in microparticle generation. Microparticle generation seems to be a well regulated process. Microparticles vary in size, phospholipid and protein composition. They have a potent pro-inflammatory effect, promote coagulation and affect vascular function. Since these processes are all involved in the pathogenesis of cardiovascular disease and circulating microparticle numbers are altered in many cardiovascular diseases, a role for microparticles in the pathogenesis of cardiovascular diseases is likely. Although hard evidence for a role of microparticles in cardiovascular diseases at present is still only limited, new evidence is accumulating rapidly to support this theory. Elucidation of the microparticle composition and the mechanisms involved in exertion of their effects will supply this evidence and enable us to develop additional intervention strategies for prevention and treatment of cardiovascular diseases.

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Year:  2003        PMID: 12909311     DOI: 10.1016/s0008-6363(03)00367-5

Source DB:  PubMed          Journal:  Cardiovasc Res        ISSN: 0008-6363            Impact factor:   10.787


  162 in total

1.  Methodology for isolation, identification and characterization of microvesicles in peripheral blood.

Authors:  Muthuvel Jayachandran; Virginia M Miller; John A Heit; Whyte G Owen
Journal:  J Immunol Methods       Date:  2011-10-29       Impact factor: 2.303

Review 2.  The involvement of circulating microparticles in inflammation, coagulation and cardiovascular diseases.

Authors:  Paolo Puddu; Giovanni M Puddu; Eleonora Cravero; Silvia Muscari; Antonio Muscari
Journal:  Can J Cardiol       Date:  2010-04       Impact factor: 5.223

Review 3.  Microparticles in stored red blood cells: submicron clotting bombs?

Authors:  Olivier Rubin; David Crettaz; Jean-Daniel Tissot; Niels Lion
Journal:  Blood Transfus       Date:  2010-06       Impact factor: 3.443

4.  A novel broadband impedance method for detection of cell-derived microparticles.

Authors:  Vadim Lvovich; Sowmya Srikanthan; Roy L Silverstein
Journal:  Biosens Bioelectron       Date:  2010-08-03       Impact factor: 10.618

5.  Keratinocyte Microvesicles Regulate the Expression of Multiple Genes in Dermal Fibroblasts.

Authors:  Ping Huang; Jiarui Bi; Gethin R Owen; Weimin Chen; Anne Rokka; Leeni Koivisto; Jyrki Heino; Lari Häkkinen; Hannu Larjava
Journal:  J Invest Dermatol       Date:  2015-08-19       Impact factor: 8.551

6.  Impact of microparticles derived from erythrocytes on fibrinolysis.

Authors:  Grigory Levin; Ekaterina Sukhareva; Athina Lavrentieva
Journal:  J Thromb Thrombolysis       Date:  2016-04       Impact factor: 2.300

7.  Using information theory to assess the communicative capacity of circulating microRNA.

Authors:  Nnenna A Finn; Charles D Searles
Journal:  Biochem Biophys Res Commun       Date:  2013-08-27       Impact factor: 3.575

Review 8.  Intercellular transport of microRNAs.

Authors:  Reinier A Boon; Kasey C Vickers
Journal:  Arterioscler Thromb Vasc Biol       Date:  2013-02       Impact factor: 8.311

9.  Critical role for the mitochondrial permeability transition pore and cyclophilin D in platelet activation and thrombosis.

Authors:  Shawn M Jobe; Katina M Wilson; Lorie Leo; Alejandro Raimondi; Jeffery D Molkentin; Steven R Lentz; Jorge Di Paola
Journal:  Blood       Date:  2007-11-07       Impact factor: 22.113

10.  Loss of estrogen receptor beta decreases mitochondrial energetic potential and increases thrombogenicity of platelets in aged female mice.

Authors:  Muthuvel Jayachandran; Claudia C Preston; Larry W Hunter; Arshad Jahangir; Whyte G Owen; Kenneth S Korach; Virginia M Miller
Journal:  Age (Dordr)       Date:  2009-11-12
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