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J Vasc Surg ; 64(6): 1825-1834.e1, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26597457

RESUMO

OBJECTIVE: Adipose-derived stem cells (ASCs) have angiogenic potential owing to their differentiation into endothelial cells and their release of angiogenic growth factors to elicit paracrine effects. In addition, control-released basic fibroblast growth factor (bFGF) sustained with a gelatin hydrogel also supports effective angiogenesis. We sought to determine if coadministration of ASCs and control-released bFGF into murine ischemic limbs facilitates angiogenesis. METHODS: Levels of growth factors in the conditioned media of ASCs cultured with or without control-released bFGF were measured by enzyme-linked immunosorbent assays. A murine ischemic hind limb model was generated and intramuscularly injected with the following: gelatin hydrogel (group 1), a high number of ASCs (group 2), control-released bFGF (group 3), a small number of ASCs and control-released bFGF (group 4), and a high number of ASCs and control-released bFGF (group 5). Macroscopic and microscopic vascular changes were evaluated until day 7 by laser Doppler perfusion imaging and histologic analyses, respectively. RESULTS: Secretion of hepatocyte growth factor, vascular endothelial growth factor, and transforming growth factor-ß1 was enhanced by control-released bFGF. Vascular improvement was achieved in groups 4 and 5 according to laser Doppler perfusion imaging. Hematoxylin and eosin staining and CD31 immunohistochemical staining demonstrated an increase in the vascular density, vessel diameter, and thickness of vessel walls in groups 4 and 5. Cells positively stained for CD146, α-smooth muscle actin, and transforming growth factor-ß1 were observed around vessel walls in groups 4 and 5. CONCLUSIONS: These findings suggest that coadministration of ASCs and control-released bFGF facilitates angiogenesis in terms of vessel maturation in a murine ischemic hind limb model.


Assuntos
Tecido Adiposo/citologia , Indutores da Angiogênese/administração & dosagem , Fator 2 de Crescimento de Fibroblastos/administração & dosagem , Isquemia/terapia , Músculo Esquelético/irrigação sanguínea , Neovascularização Fisiológica/efeitos dos fármacos , Transplante de Células-Tronco , Indutores da Angiogênese/química , Animais , Células Cultivadas , Terapia Combinada , Meios de Cultivo Condicionados/metabolismo , Preparações de Ação Retardada , Modelos Animais de Doenças , Portadores de Fármacos , Fator 2 de Crescimento de Fibroblastos/química , Gelatina/química , Proteínas de Fluorescência Verde/biossíntese , Proteínas de Fluorescência Verde/genética , Fator de Crescimento de Hepatócito/metabolismo , Membro Posterior , Humanos , Hidrogéis , Isquemia/metabolismo , Isquemia/fisiopatologia , Masculino , Camundongos Endogâmicos C57BL , Camundongos Transgênicos , Recuperação de Função Fisiológica , Fluxo Sanguíneo Regional , Fatores de Tempo , Fator de Crescimento Transformador beta1/metabolismo , Fator A de Crescimento do Endotélio Vascular/metabolismo
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