对巨核细胞进行重新编程,使血小板成为递送载体。

Farhana Islam, Shwan B Javdan, Mitchell R Lewis, James D Craig, Han Wu, Tara L Deans
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引用次数: 0

摘要

我们开发了一种有效生成工程血小板的方法,通过对巨核细胞(血小板的祖细胞)进行重新编程,在分化过程中可以用任何重组治疗蛋白填充工程血小板。为了证明这种方法的多功能性,我们装载了细胞质和分泌蛋白,这些蛋白可以作为活性酶输送到受体细胞,在血小板活化时释放,或者随着时间的推移由血小板持续分泌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Programming megakaryocytes to produce engineered platelets for delivering non-native proteins.

Platelets are anucleate cells naturally filled with secretory granules that store large amounts of protein to be released in response to certain physiological conditions. Cell engineering can endow platelets with the ability to deliver non-native proteins by modifying them as they develop during the cell fate process. This study presents a strategy to efficiently generate mouse platelets from pluripotent stem cells and demonstrates their potential as bioengineered protein delivery platforms. By modifying megakaryocytes, the progenitor cells of platelets, we successfully engineered platelets capable of packaging and delivering non-native proteins. These engineered platelets can offer flexible delivery platforms to release non-native proteins in a controlled manner upon activation when packaged into α-granules or deliver active enzymes to genetically alter recipient cells. Our findings highlight platelets as a promising tool for protein delivery in cell therapy applications.

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