首页|Thylakoid engineered M2 macrophage for sonodynamic effect promoted cell therapy of early atherosclerosis

Thylakoid engineered M2 macrophage for sonodynamic effect promoted cell therapy of early atherosclerosis

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Atherosclerosis is the most common cause of cardiovascular diseases that contribute to the major morbidity worldwide,but still lacking of effective treatment strategy.Here,a hybrid cell is constructed for the sonodynamic effect promoted cell therapy of early atherosclerosis by fusing M2 macrophages with thylakoid(TK)membranes.After systemic administration,the obtained TK-M2 actively accumulates in the early atherosclerotic plaques,wherein M2 macrophages relieve the cholesterol accumulation and the inflammation in the foam cells.Meanwhile,the TK membranes decorated on the M2 macrophages exhibit both type Ⅰ and type II sonodynamic effects under ultrasound(US)activation,inducing the direct apoptosis of foam cells.The cooperation of M2 and TK leads to significant outcome in eliminating atherosclerotic plaques without obvious side-effects,providing a new avenue for atherosclerosis treatment.

atherosclerosisthylakoidultrasoundM2 macrophage

Guanghao Wu、Changwen Mu、Qianru Zhao、Yao Lei、Ran Cheng、Weidong Nie、Jiamin Qu、Yuping Dong、Ruili Yang、Haiyan Xie

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School of Materials Science and Engineering,Beijing Institute of Technology,Beijing 100081,China

School of Life Science,Beijing Institute of Technology,Beijing 100081,China

School of Stomatology,Peking University,Beijing 100081,China

State Key Laboratory of Natural and Biomimetic Drugs,School of Pharmaceutical Sciences,Chemical Biology Center,Peking University,Beijing 100191,China

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National Science Fund for Distinguished Young ScholarsNational Natural Science Foundation of ChinaNational Natural Science Foundation of ChinaChina Postdoctoral Science FoundationChina Postdoctoral Science FoundationBiological &Medical Engineering Core Facilities(Beijing Institute of Technology)

2202540121874011221040052021TQ00372021M690405

2024

纳米研究(英文版)

纳米研究(英文版)

CSTPCD
ISSN:
年,卷(期):2024.17(4)
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