Journal
JOINT BONE SPINE
Volume 80, Issue 1, Pages 70-76Publisher
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.jbspin.2012.02.015
Keywords
Avascular osteonecrosis; Endothelial progenitor cells; Endothelial colony forming cells; Glucocorticoid
Categories
Funding
- National Natural Science Foundation of China [30973044, 81101375]
- Natural Science Foundation of Hubei Province of China [2009CDB046]
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Objectives: This study examined whether abnormalities of early EPCs and endothelial colony forming cells (ECFCs) are present and compared their functions in glucocorticoid (GC)-induced avascular osteonecrosis of the femoral head (ANFH). Methods: Early EPCs and endothelial colony forming cells (ECFCs) were obtained from 33 patients with glucocorticoid-induced ANFH and 33 age- and sex-matched control subjects. Cells were isolated, in vitro cultured and studied by Flow Cytometry and Immunofluorescence. Colony-forming unit counts were observed from 33 patients and 33 healthy controls. Growth kinetics, migratory capacity to multiple chemo-attractants, in vitro tube formation capacity and cytokine (vascular endothelial growth factor and stromal cell-derived factor-1) levels in supernatants of two types of EPCs were assayed in ANFH patients and matched controls (n = 4). Results: Mean numbers of colonies formed by both types of EPCs were decreased in ANFH patients (Early EPCs: 2.42 +/- 1.46 versus 4.52 +/- 2.00, p < 0.05; ECFCs: 0.62 +/- 0.55 versus 1.12 +/- 0.82, p < 0.05,). Early EPCs from ANFH patients showed impaired migratory capacity (63.8 +/- 11.7 versus 152.3 +/- 12.4, p < 0.001) and VEGF secretion (50.8 +/- 7.2 pg/ml versus 62.8 +/- 10.1 pg/ml, p < 0.05). ECFCs from ANFH patients showed decreased tube formation capacity (7.1 +/- 2.7 versus 23.8 +/- 4.3, p < 0.001) and proliferation. Discussion: Early EPCs and ECFCs were impaired in number and function in GC-induced ANFH, and their distinct reduced capacity profiles might reflect different roles they played in endothelial dysfunction of GC-induced ANFH. (c) 2012 Published by Elsevier Masson SAS on behalf of the Societe Francaise de Rhumatologie.
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