Controlled protein delivery in the generation of microvascular networks

被引:8
作者
Andrejecsk, Jillian W. [1 ]
Chang, William G. [2 ,3 ]
Pober, Jordan S. [4 ,5 ]
Saltzman, W. Mark [1 ]
机构
[1] Yale Univ, Dept Biomed Engn, New Haven, CT 06511 USA
[2] Yale Univ, Sch Med, Dept Med, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Nephrol Sect, New Haven, CT 06520 USA
[4] Yale Univ, Sch Med, Dept Immunobiol, Dept Pathol, New Haven, CT 06520 USA
[5] Yale Univ, Sch Med, Dept Dermatol, New Haven, CT 06520 USA
基金
美国国家卫生研究院;
关键词
Protein delivery; Microvascular network; Angiogenesis; Vascularization; Stabilization; Tissue engineering; ENDOTHELIAL GROWTH-FACTOR; ENGINEERED VASCULAR GRAFTS; SMOOTH-MUSCLE-CELLS; PROOF-OF-CONCEPT; IN-VIVO; BLOOD-VESSELS; PDGF-BB; INFLAMMATORY ANGIOGENESIS; MYOCARDIAL-INFARCTION; ARTERIOLE FORMATION;
D O I
10.1007/s13346-012-0122-y
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
Rapid induction and stabilization of new microvascular networks is essential for the proper functioning of engineered tissues. Many efforts to achieve this goal have used proangiogenic proteins-such as vascular endothelial growth factors-to induce the formation of new microvessels. These proteins have demonstrated promise in improving vascularization, but it is also clear that the spatial and temporal presentation of these signals is important for achieving proper vascular function. Delivery systems that present proteins in a localized and sustained manner can promote the formation and stabilization of microvascular networks by precisely presenting proangiogenic proteins at desired locations, and for specified durations. Further, these systems allow for some control over the sequence of release of multiple proteins, and it has become clear that such coordination is critical for the development of fully functional and mature vascular structures. This review focuses on the actions of proangiogenic proteins and the innovations in controlled release technologies that precisely deliver these to stimulate microvascular network formation and stabilization.
引用
收藏
页码:75 / 88
页数:14
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