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Antiendothelial Cell Antibodies Induce Apoptosis of Bone Marrow Endothelial Progenitors in Systemic Sclerosis

Authors :
DEL PAPA, NICOLETTA
QUIRICI, NADIA
SCAVULLO, CINZIA
GIANELLI, UMBERTO
CORTI, LAURA
VITALI, CLAUDIO
FERRI, CLODOVEO
GIUGGIOLI, DILIA
MANFREDI, ANDREINA
MAGLIONE, WANDA
ONIDA, FRANCESCO
COLACI, MICHELE
BOSARI, SILVANO
LAMBERTENGHI DELILIERS, GIORGIO
Source :
Journal of Rheumatology; October 2010, Vol. 37 Issue: 10 p2053-2063, 11p
Publication Year :
2010

Abstract

OBJECTIVE: Patients with systemic sclerosis (SSc) have significantly fewer and functionally impaired endothelial progenitor cells (EPC) in peripheral blood and bone marrow; further, endothelial apoptosis seems to play a primary role in the pathogenesis of vascular damage. We investigated whether the failure of bone marrow EPC is related to their apoptotic phenotype and analyzed the possible mechanisms inducing apoptosis. METHODS: The presence of apoptotic cells was investigated in bone marrow aspirates taken from patients with SSc; microvessel density (MVD) and the immunohistochemical expression of vascular endothelial growth factor (VEGF) were also measured in bone marrow biopsies. A correlation between EPC apoptosis and the presence of antiendothelial cell antibodies (AECA) was also investigated. RESULTS: We confirmed the presence of bone marrow EPC dysfunction in SSc, while hematopoiesis was not impaired. Bone marrow studies showed a high percentage of apoptotic progenitors, no signs of fibrosis or an altered MVD, and an increased VEGF index. The patients’ bone marrow plasma showed significant titers of AECA, and their presence correlated with that of apoptotic progenitors. These findings were further confirmed by an in vitro assay in which the apoptosis of normal progenitors was induced by the addition of AECA+ purified IgG. CONCLUSION: Our results showed that apoptosis in patients with SSc involves the source compartment of endothelial progenitors and correlates with AECA activity. These findings support the hypothesis that AECA may play a pathogenetic role by affecting the bone marrow EPC machinery that should repair the peripheral vascular lesions.

Details

Language :
English
ISSN :
0315162X and 14992752
Volume :
37
Issue :
10
Database :
Supplemental Index
Journal :
Journal of Rheumatology
Publication Type :
Periodical
Accession number :
ejs22299153