血小板
体内
凝结
化学
血小板活化
细胞生物学
医学
生物
免疫学
内科学
生物技术
作者
Pei‐Pei Yang,Kuo Zhang,Pingping He,Yu Fan,Xuejiao J. Gao,Xingfa Gao,Ziming Chen,Da‐Yong Hou,Yuan Li,Yu Yi,Dong‐Bing Cheng,Jingping Zhang,Linqi Shi,Xian‐Zheng Zhang,Lei Wang,Hao Wang
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2020-05-27
卷期号:6 (22)
被引量:76
标识
DOI:10.1126/sciadv.aaz4107
摘要
Platelets play a critical role in the regulation of coagulation, one of the essential processes in life, attracting great attention. However, mimicking platelets for in vivo artificial coagulation is still a great challenge due to the complexity of the process. Here, we design platelet-like nanoparticles (pNPs) based on self-assembled peptides that initiate coagulation and form clots in blood vessels. The pNPs first bind specifically to a membrane glycoprotein (i.e., CD105) overexpressed on angiogenetic endothelial cells in the tumor site and simultaneously transform into activated platelet-like nanofibers (apNFs) through ligand-receptor interactions. Next, the apNFs expose more binding sites and recruit and activate additional pNPs, forming artificial clots in both phantom and animal models. The pNPs are proven to be safe in mice without systemic coagulation. The self-assembling peptides mimic platelets and achieve artificial coagulation in vivo, thus providing a promising therapeutic strategy for tumors.
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