Polyurethane conjugating TGF-beta on surface impacts local inflammation and endoplasmic reticulum stress in skeletal muscle
Polyurethane conjugating TGF-beta on surface impacts local inflammation and endoplasmic reticulum stress in skeletal muscle
复制标题
表面结合 TGF-β 的聚氨酯影响骨骼肌局部炎症和内质网应激
DOI:
10.1002/jbm.a.35999
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发表时间:
2017
影响因子:
4.9
通讯作者:
Liao Hua
中科院分区:
文献类型:
--
作者:
Shi D;an;Xiao Jiangwei;Gu Ruicai;Wu Gang;Liao Hua
The synthesized short peptide‐polymers would provide key functions for tissue regeneration and repair, through enriching bioactive molecules on polymers or releasing these molecules pre‐conjugated on the materials. We have developed a degradable polyurethane (PU) bearing HSNGLPL peptide, which has affinity binding ability to transforming growth factor‐betas (TGF‐β). For deeply understanding spatial release of TGF‐β from the PU polymers and its localized bioactivity, quartz crystal microbalance (QCM) and Elisa test were used to verify TGF‐β binding capacitiesin vitroandin vivo. The PU polymers, with or without pre‐conjugating of TGF‐β, were implanted into gastronomies muscle (GN) of C57BL/6 mice, for addressing TGF‐β release from the polymers and its bio‐regulating functionin vivo. QCM result shows that PU bearing HSNGLPL peptide has affinity binding ability to TGF‐βin vitro. Intramuscular implanting experiment further supports the enrichment efficiency of TGF‐β on PU polymersin vivo. The detecting data involving intramuscular inflammatory infiltration triggered by the implants, myofiber regeneration, muscular fibrosis degree, and activation of endoplasmic reticulum stress (ER stress), evidence TGF‐β can be released from PU polymers, and exerts regulating effects on the material‐induced inflammation. Thus, our present results suggest it is feasible to improve biocompatibility of PU polymersin vivo, by pre‐bearing bioactive molecules on materials before the implanting. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 1156–1165, 2017.