首页> 外文OA文献 >Intracellular Release of 17-β Estradiol from Cationic Polyamidoamine Dendrimer Surface-Modified Poly (Lactic-co-Glycolic Acid) Microparticles Improves Osteogenic Differentiation of Human Mesenchymal Stromal Cells
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Intracellular Release of 17-β Estradiol from Cationic Polyamidoamine Dendrimer Surface-Modified Poly (Lactic-co-Glycolic Acid) Microparticles Improves Osteogenic Differentiation of Human Mesenchymal Stromal Cells

机译:从阳离子型聚酰胺酰胺树状大分子表面修饰的聚(乳酸-共-乙醇酸)微粒中释放17-β雌二醇可改善人间质基质细胞的成骨分化

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摘要

Human bone marrow mesenchymal stromal cells (MSCs) are considered a potential cell source for MSC-based bone regeneration, but improvements in the proliferation and differentiation capacity of MSCs are necessary for practical applications. Estrogen effectively improves MSC capabilities and has strong potential as a regulator of MSCs. The aim of this study was to develop a delivery system that provides intracellular release of estrogen and test its ability to improve osteogenic differentiation of MSCs. Biodegradable poly (lactic-co-glycolic acid) (PLGA) microparticles were developed that entrap 17-β estradiol (E2) and provide intracellular release of E2. The results show that we can prepare PLGA particles with efficient loading of E2 and maintain release of E2 up to 7 days. Surface modifying E2-loaded PLGA particles with cationic polyamidoamine dendrimers enabled increased uptake by human MSCs. Human MSC uptake of the E2-loaded PLGA particles significantly upregulates osteogenic differentiation markers of alkaline phosphatase and osteocalcin. In conclusion, cationic-modified PLGA particles can serve as a tool for intracellular delivery of estrogen to effectively execute estrogen regulation of MSCs. This approach has the potential to improve the osteogenic capabilities of MSCs and to develop appropriate environments of implantation for MSC-based bone tissue engineering.
机译:人骨髓间充质基质细胞(MSC)被认为是基于MSC的骨再生的潜在细胞来源,但实际应用中必须提高MSC的增殖和分化能力。雌激素可有效提高MSC的能力,并具有作为MSC调节剂的强大潜力。这项研究的目的是开发一种输送系统,该系统可提供细胞内雌激素的释放,并测试其改善MSC成骨分化的能力。已开发出可生物降解的聚乳酸-乙醇酸共聚物(PLGA)微粒,可捕获17-β雌二醇(E2)并提供E2在细胞内的释放。结果表明,我们可以制备有效负载E2的PLGA颗粒,并保持E2释放长达7天。表面改性的E2负载的PLGA粒子与阳离子聚酰胺酰胺树状大分子的结合使人MSC的摄取增加。人MSC对E2负载的PLGA颗粒的摄取显着上调了碱性磷酸酶和骨钙素的成骨分化标记。总之,阳离子修饰的PLGA颗粒可作为细胞内雌激素递送工具,以有效地执行MSC的雌激素调节。这种方法有可能改善MSC的成骨能力,并为基于MSC的骨组织工程开发合适的植入环境。

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