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ATVB in Focus

Microparticles
Series Editors: Chantal M. Boulanger and Franoise Dignat-George

Articles in this series


Boulanger CM, Dignat-George F. Microparticles: an introduction. Arterioscler Thromb Vasc Biol. 2011;31:23.
Tushuizen ME, Diamant M, Sturk A, Nieuwland R. Cell-derived microparticles in the pathogenesis of cardiovascu-
lar disease: friend or foe? Arterioscler Thromb Vasc Biol. 2011;31:4 9.
Shai E, Varon D. Development, Cell Differentiation, AngiogenesisMicroparticles and their roles in angiogenesis.
Arterioscler Thromb Vasc Biol. 2011;31:10 14.
Morel O, Jesel L, Freyssinet J-M, Toti F. Cellular mechanisms underlying the formation of circulating micropar-
ticles. Arterioscler Thromb Vasc Biol. 2011;31:1526.
Dignat-George F, Boulanger CM. The many faces of endothelial microparticles. Arterioscler Thromb Vasc
Biol. 2011;31:2733.

Microparticles: An Introduction
Chantal M. Boulanger, Francoise Dignat-George
Downloaded from http://atvb.ahajournals.org/ by guest on May 26, 2017

T he notion that cells shed small membrane vesicles


from their plasma membrane was reported some 40
years ago, and for many years this process was described
populations of circulating microparticles and studies on
their generation have greatly contributed to our knowledge
of the mechanisms involved in the loss of membrane
as the release of cell dust. However, the past decade has phospholipid asymmetry. Interestingly, Scotts syndrome
seen an unprecedented interest in membrane vesicles in is a rare congenital bleeding disorder that presents as a
many fields of biology, including vascular biology and defect in platelet membrane remodeling. Morel et al also
thrombosis. Consequently, the term cell dust has been draw our attention to the role of intracellular calcium
replaced by the term microparticles to describe submicron concentration in cytoskeleton reorganization during amin-
membrane vesicles shed from activated or apoptotic cells. ophospholipid externalization. Whether or not these mech-
Exciting findings have further demonstrated the unex- anisms regulating membrane and cytoskeleton remodeling
pected biological impact of these microparticles on cellular in platelets also hold true for microparticle formation in
cross-talk and their contribution to inflammation, throm- other cell types remains to be established. The pathophys-
bosis, and angiogenesis. A thorough investigation of the iological relevance of microparticle formation is high-
mechanisms governing their release and their interaction lighted in the review by Zwicker et al, that focuses on the
with target cells is now required for a proper understanding contribution of microparticles bearing tissue factor to
of their contribution to disease progression or repair thrombus formation. The notion of a blood-borne tissue
mechanisms. factor conveyed by circulating microparticles represents
The review series begins with an article by Morel et al an alternative mechanism for activation of blood coagula-
summarizing the state of the art on the mechanisms tion. However, much debate still exists regarding the
governing the formation of circulating microparticles. presence of tissue factor activity on circulating micropar-
Platelet-derived microparticles represent one of the major ticles, despite the general consensus that tissue factor
antigen is measurable in plasma. The third review article of
this series focuses on microparticles of endothelial origin.
Although they represent a minor population of the overall
From INSERM, U970, Paris Cardiovascular Research Center,
Paris, France (C.B.); Universite Paris Descartes, UMR-S970, Paris, pool of circulating microparticles, endothelial micropar-
France (C.B.); INSERM UMR-608, Pathophysiology of the Endothe- ticles present a surrogate marker of activated/apoptotic
lium, UFR de Pharmacie, Universite de la Mediterranee, Marseille, endothelial cells. Depending on the cause of endothelial
France (F.D.-G.); Department of Hematology and Immunology,
Conception Hospital, Marseille, France (F.D.-G.).
activation, they display specific phenotypes that could
Correspondence to Francoise Dignat-George, MD, PhD, INSERM contribute to their multifaceted effects on vascular
UMR-608, Pathophysiology of the Endothelium, UFR de Pharmacie, homeostasis.
27 bd Jean Moulin, 13385 Marseille Cedex 05, France (e-mail
francoise.dignat-george@univmed.fr) or Chantal M. Boulanger, PhD,
The next set of reviews addresses and reviews the role of
INSERM UMR-970, Paris Cardiovascular Research Center, 56 rue microparticles in the development of cardiovascular dis-
Leblanc, 75373 Paris Cedex 15, France. E-mail chantal.boulanger@ eases and potential repair mechanisms. Tushuizen et al
inserm.fr
2010 American Heart Association, Inc.
discuss the potential deleterious or beneficial effects of
(Arterioscler Thromb Vasc Biol. 2011;31:2-3.) circulating microparticles on the vessel wall. They also
Arterioscler Thromb Vasc Biol is available at http://atvb.ahajournals.org highlight the notion that plasma levels of specific su-
DOI: 10.1161/ATVBAHA.110.220095 bpopulations of microparticles are valuable surrogate
2
Boulanger and Dignat-George Introduction to Review Series on Microparticles 3

markers of vascular health and that evidence suggests that This review series on microparticles will introduce Arte-
they have potential prognostic value in cardiovascular riosclerosis, Thrombosis, and Vascular Biology readers to the
diseases. Finally, Shai and Varon discuss the contribution field of shed-membrane vesicles and their wide spectrum of
of microparticles to tissue repair and pathological angio- actions in cardiovascular homeostasis. The ubiquitous forma-
genesis, such as cancer angiogenesis or diabetic retinopa- tion of these vesicles certainly raises questions regarding their
thy. The mechanisms governing these microparticle effects unforeseen contribution to a large number of biological
involve direct activation of signaling pathways, transfer of responses. A better understanding of mechanisms governing
growth factors or new transcripts, or pericellular proteo- their generation and of their potential to reprogram remote
lytic activities mediated by serine proteases and cells in pathological conditions represents a new dimension in
metalloproteases. cellular communication.
Downloaded from http://atvb.ahajournals.org/ by guest on May 26, 2017
Microparticles: An Introduction
Downloaded from http://atvb.ahajournals.org/ by guest on May 26, 2017

Chantal M. Boulanger and Franoise Dignat-George

Arterioscler Thromb Vasc Biol. 2011;31:2-3


doi: 10.1161/ATVBAHA.110.220095
Arteriosclerosis, Thrombosis, and Vascular Biology is published by the American Heart Association, 7272
Greenville Avenue, Dallas, TX 75231
Copyright 2010 American Heart Association, Inc. All rights reserved.
Print ISSN: 1079-5642. Online ISSN: 1524-4636

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