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聚环氧乙烷-聚环氧丙烷二嵌段共聚物在体外可保护成肌细胞免受低渗应激,这取决于共聚物的尺寸、组成和结构。

PEO-PPO Diblock Copolymers Protect Myoblasts from Hypo-Osmotic Stress In Vitro Dependent on Copolymer Size, Composition, and Architecture.

作者信息

Kim Mihee, Haman Karen J, Houang Evelyne M, Zhang Wenjia, Yannopoulos Demetris, Metzger Joseph M, Bates Frank S, Hackel Benjamin J

机构信息

Department of Chemical Engineering and Materials Science, ‡Department of Integrative Biology and Physiology, and §Department of Medicine, Cardiovascular Division, University of Minnesota , Minneapolis, Minnesota 55455, United States.

出版信息

Biomacromolecules. 2017 Jul 10;18(7):2090-2101. doi: 10.1021/acs.biomac.7b00419. Epub 2017 Jun 14.

Abstract

Poloxamer 188, a triblock copolymer of poly(ethylene oxide) (PEO) and poly(propylene oxide) (PPO), protects cellular membranes from various stresses. Though numerous block copolymer variants exist, evaluation of alternative architecture, composition, and size has been minimal. Herein, cultured murine myoblasts are exposed to the stresses of hypotonic shock and isotonic recovery, and membrane integrity was evaluated by quantifying release of lactate dehydrogenase. Comparative evaluation of a systematic set of PEO-PPO diblock and PEO-PPO-PEO triblock copolymers demonstrates that the diblock architecture can be protective in vitro. Short PPO blocks hinder protection with >9 PPO units needed for protection at 150 μM and >16 units needed at 14 μM. Addition of a tert-butyl end group enhances protection at reduced concentration. When the end group and PPO length are fixed, increasing the PEO length improves protection. This systematic evaluation establishes a new in vitro screening tool for evaluating membrane-sealing amphiphiles and provides mechanistic insight to guide future copolymer design for membrane stabilization in vivo.

摘要

泊洛沙姆188是一种由聚环氧乙烷(PEO)和聚环氧丙烷(PPO)组成的三嵌段共聚物,可保护细胞膜免受各种应激。尽管存在许多嵌段共聚物变体,但对其替代结构、组成和尺寸的评估却很少。在此,将培养的小鼠成肌细胞暴露于低渗休克和等渗恢复应激下,并通过定量乳酸脱氢酶的释放来评估膜的完整性。对一组系统的PEO-PPO二嵌段和PEO-PPO-PEO三嵌段共聚物的比较评估表明,二嵌段结构在体外具有保护作用。短的PPO嵌段会阻碍保护作用,在150μM时需要>9个PPO单元才能起到保护作用,在14μM时需要>16个单元。添加叔丁基端基可在较低浓度下增强保护作用。当端基和PPO长度固定时,增加PEO长度可改善保护作用。这种系统评估建立了一种新的体外筛选工具,用于评估膜封闭两亲物,并为指导未来体内膜稳定化共聚物设计提供了机制性见解。

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