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Materials roles for promoting angiogenesis in tissue regeneration

期刊

PROGRESS IN MATERIALS SCIENCE
卷 117, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pmatsci.2020.100732

关键词

Angiogenesis; Tissue regeneration; Materials properties; Delivery; Cell engineering

资金

  1. National Research Foundation (NRF) , Republic of Korea (Global Research Lab Program) [20150093829, NRF2018R1A2B3003446, NRF2018K1A4A3A01064257, 2019R1A6A1A11034536, NRF2019R1C1C1002490]
  2. National Research Foundation of Korea [2015K1A1A2032163, 2018R1A2B3003446, 5120200513602, 2018K1A4A3A01064257] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This article discusses the importance of proangiogenic efforts in tissue repair and regeneration, focusing on the pivotal roles of engineered matrices in stimulating angiogenesis processes. The design and tuning of matrices for the proper presentation of growth factors and the sustained release of angiogenic molecules are crucial for tissue repair therapies.
Enabling angiogenesis is critical for the success of tissue repair therapies and the fate of tissueengineered constructs. Although many biochemical signaling molecules have been used, their biological functions in vivo are known to be limited, mainly due to their short lifetime and poor activity. Matrices (or engineered biomaterials), beyond the biochemical signals, play pivotal roles in stimulating angiogenic processes. Here we discuss the proangiogenic effort taken to repair and regenerate various tissues including skin, bone, muscle and nerve, focusing on the roles of engineered matrices. This includes the design of pore structure and physico-chemical properties (nanotopology, stiffness, chemistry and degradability), the tailoring of matrices for proper presentation of growth factors and their crosstalks with adhesion ligands, the controlled and sustained delivery of angiogenic molecules and metallic ions, and the engineering of cells and construction of prevascularized tissues. Collectively, the materials-driven strategies are envisaged

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