Promoting Angiogenesis Using Immune Cells for Tissue-Engineered Vascular Grafts

被引:4
作者
Wang, Li [1 ,2 ]
Wei, Xinbo [2 ]
Wang, Yuqing [1 ,2 ]
机构
[1] Anhui Univ Chinese Med, Sch Integrated Chinese & Western Med, Hefei 230012, Peoples R China
[2] Beihang Univ, Beijing Adv Innovat Ctr Biomed Engn, Sch Biol Sci & Med Engn, Key Lab Biomech & Mechanobiol,Minist Educ, Beijing 100083, Peoples R China
关键词
Immune cells; Tissue-engineered vascular grafts; Vascularization; Macrophages; Biomaterials; SMOOTH-MUSCLE-CELLS; ENDOTHELIAL GROWTH-FACTOR; MESENCHYMAL STEM-CELL; COLLATERAL VESSEL DEVELOPMENT; IN-SITU ENDOTHELIALIZATION; ADULT PROGENITOR CELLS; FOREIGN-BODY REACTION; NATURAL-KILLER-CELLS; BONE-MARROW; MACROPHAGE PHENOTYPE;
D O I
10.1007/s10439-023-03158-5
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Implantable tissue-engineered vascular grafts (TEVGs) usually trigger the host reaction which is inextricably linked with the immune system, including blood-material interaction, protein absorption, inflammation, foreign body reaction, and so on. With remarkable progress, the immune response is no longer considered to be entirely harmful to TEVGs, but its therapeutic and impaired effects on angiogenesis and tissue regeneration are parallel. Although the implicated immune mechanisms remain elusive, it is certainly worthwhile to gain detailed knowledge about the function of the individual immune components during angiogenesis and vascular remodeling. This review provides a general overview of immune cells with an emphasis on macrophages in light of the current literature. To the extent possible, we summarize state-of-the-art approaches to immune cell regulation of the vasculature and suggest that future studies are needed to better define the timing of the activity of each cell subpopulation and to further reveal key regulatory switches.
引用
收藏
页码:660 / 678
页数:19
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