Improved Angiogenesis in Response to Localized Delivery of Macrophage-Recruiting Molecules.

Improved Angiogenesis in Response to Localized Delivery of Macrophage-Recruiting Molecules.
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DOI:
10.1371/journal.pone.0131643
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发表时间:
2015
期刊:
影响因子:
3.7
通讯作者:
Dickinson ME
Dickinson ME
中科院分区:
综合性期刊3区
文献类型:
--
作者:
Hsu CW;Poché RA;Saik JE;Ali S;Wang S;Yosef N;Calderon GA;Scott L Jr;Vadakkan TJ;Larina IV;West JL;Dickinson ME

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Successful engineering of complex organs requires improved methods to promote rapid and stable vascularization of artificial tissue scaffolds. Toward this goal, tissue engineering strategies utilize the release of pro-angiogenic growth factors, alone or in combination, from biomaterials to induce angiogenesis. In this study we have used intravital microscopy to define key, dynamic cellular changes induced by the release of pro-angiogenic factors from polyethylene glycol diacrylate hydrogels transplanted in vivo. Our data show robust macrophage recruitment when the potent and synergistic angiogenic factors, PDGFBB and FGF2 were used as compared with VEGF alone and intravital imaging suggested roles for macrophages in endothelial tip cell migration and anastomosis, as well as pericyte-like behavior. Further data from in vivo experiments show that delivery of CSF1 with VEGF can dramatically improve the poor angiogenic response seen with VEGF alone. These studies show that incorporating macrophage-recruiting factors into the design of pro-angiogenic biomaterial scaffolds is a key strategy likely to be necessary for stable vascularization and survival of implanted artificial tissues.
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