Circulating endothelial cells, microparticles and progenitors: key players towards the definition of vascular competence

被引:192
作者
Sabatier, F. [1 ,2 ,4 ]
Camoin-Jau, L. [1 ,2 ,3 ]
Anfosso, F. [1 ,2 ]
Sampol, J. [1 ,2 ]
Dignat-George, F. [1 ,2 ,3 ]
机构
[1] Aix Marseille Univ, F-13385 Marseille, France
[2] Hop Enfants La Timone, INSERM, U608, F-13385 Marseille, France
[3] Univ La Concept, Ctr Hosp, Hematol Lab, Marseille, France
[4] CHU Concept, INSERM, CIC BT 510, Lab Culture & Therapie Cellulaire, Marseille, France
关键词
circulating endothelial cells; endothelial microparticles; endothelial progenitor cells; endothelial injury; repair; endothelial biomarkers; vascular competence; SHED MEMBRANE MICROPARTICLES; SYSTEMIC-LUPUS-ERYTHEMATOSUS; ACUTE MYOCARDIAL-INFARCTION; TYPE-2; DIABETES-MELLITUS; ACUTE ISCHEMIC-STROKE; VON-WILLEBRAND-FACTOR; BONE-MARROW; IN-VITRO; PERIPHERAL-BLOOD; TISSUE FACTOR;
D O I
10.1111/j.1582-4934.2008.00639.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Introduction Dynamics between endothelial injury and repair: the response to injury theory 'revisited' Emerging biomarkers reflecting the dynamics between endothelial injury and repair: from pathophysiology to clinical testing. Circulating endothelial cells Endothelial microparticles Endothelial progenitor cells Endothelial lesion versus regeneration: towards the definition of 'vascular competence' Conclusion The balance between lesion and regeneration of the endothelium is critical for the maintenance of vessel integrity. Exposure to cardiovascular risk factors (CRF) alters the regulatory functions of the endothelium that progresses from a quiescent state to activation, apoptosis and death. In the last 10 years, identification of circulating endothelial cells (CEC) and endothelial-derived microparticles (EMP) in the circulation has raised considerable interest as non-invasive markers of vascular dysfunction. Indeed, these endothelial-derived biomarkers were associated with most of the CRFs, were indicative of a poor clinical outcome in atherothrombotic disorders and correlated with established parameters of endothelial dysfunction. CEC and EMP also behave as potential pathogenic vectors able to accelerate endothelial dysfunction and promote disease progression. The endothelial response to injury has been enlarged by the discovery of a powerful physiological repair process based on the recruitment of circulating endothelial progenitor cells (EPC) from the bone marrow. Recent studies indicate that reduction of EPC number and function by CRF plays a critical role in the progression of cardiovascular diseases. This EPC-mediated repair to injury response can be integrated into a clinical endothelial phenotype defining the 'vascular competence' of each individual. In the future, provided that standardization of available methodologies could be achieved, multimarker strategies combining CEC, EMP and EPC levels as integrative markers of 'vascular competence' may offer new perspectives to assess vascular risk and to monitor treatment efficacy.
引用
收藏
页码:454 / 471
页数:18
相关论文
共 159 条
[1]   Mobilizing endothelial progenitor cells [J].
Aicher, A ;
Zeiher, AM ;
Dimmeler, S .
HYPERTENSION, 2005, 45 (03) :321-325
[2]   Phenotypic heterogeneity of the endothelium II. Representative vascular beds [J].
Aird, William C. .
CIRCULATION RESEARCH, 2007, 100 (02) :174-190
[3]   Impact of immunosuppressive treatment on endothelial biomarkers after kidney transplantation [J].
Al-Massarani, G. ;
Vacher-Coponat, H. ;
Paul, P. ;
Widemann, A. ;
Arnaud, L. ;
Loundou, A. ;
Robert, S. ;
Berland, Y. ;
Dignat-George, F. ;
Camoin-Jau, L. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2008, 8 (11) :2360-2367
[4]   Circulating endothelial microparticles are associated with vascular dysfunction in patients with end-stage renal failure [J].
Amabile, N ;
Guérin, AP ;
Leroyer, A ;
Mallat, Z ;
Nguyen, C ;
Boddaert, J ;
London, GM ;
Tedgui, A ;
Boulanger, CM .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2005, 16 (11) :3381-3388
[5]   Circulating endothelial microparticle levels predict hemodynamic severity of pulmonary hypertension [J].
Amabile, Nicolas ;
Heiss, Christian ;
Real, Wendy May ;
Minasi, Petros ;
McGlothlin, Dana ;
Rame, Eduardo J. ;
Grossman, William ;
De Marco, Teresa ;
Yeghiazarians, Yerem .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2008, 177 (11) :1268-1275
[6]   Induction of microparticle- and cell-associated intravascular tissue factor in human endotoxemia [J].
Aras, O ;
Shet, A ;
Bach, RR ;
Hysjulien, JL ;
Slungaard, A ;
Hebbel, RP ;
Escolar, G ;
Jilma, B ;
Key, NS .
BLOOD, 2004, 103 (12) :4545-4553
[7]   Endothelial progenitor cells for postnatal vasculogenesis [J].
Asahara, T ;
Kawamoto, A .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2004, 287 (03) :C572-C579
[8]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[9]   Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization [J].
Asahara, T ;
Masuda, H ;
Takahashi, T ;
Kalka, C ;
Pastore, C ;
Silver, M ;
Kearne, M ;
Magner, M ;
Isner, JM .
CIRCULATION RESEARCH, 1999, 85 (03) :221-228
[10]   Endothelial progenitor cell proliferation and differentiation is regulated by erythropoietin - Rapid communication [J].
Bahlmann, FH ;
DeGroot, K ;
Duckert, T ;
Niemczyk, E ;
Bahlmann, E ;
Boehm, SM ;
Haller, H ;
Fliser, D .
KIDNEY INTERNATIONAL, 2003, 64 (05) :1648-1652