胶原蛋白和硫酸肝素涂层在体外和体内不同程度地改变细胞增殖和附着。

TECHNOLOGY Pub Date : 2016-09-01 Epub Date: 2016-01-07 DOI:10.1142/S2339547816400033
Christopher M Walthers, Chase J Lyall, Alireza K Nazemi, Puneet V Rana, James C Y Dunn
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引用次数: 1

摘要

组织工程是应用于肠道疾病治疗的一个创新研究领域。工程平滑肌需要致密的平滑肌组织和强健的血管来支持收缩。本研究的目的是利用硫酸肝素(HS)和胶原包被增加平滑肌细胞(SMCs)与支架的附着,提高其植入后的存活率。体外培养2周、4周和6周以及体内培养2周和6周后,对生物包被支架上生长的SMCs的成熟度和细胞数量进行评估。植入物的血管化也被评估。胶原包被支架增加了培养中SMCs的附着、生长和成熟。与体外培养的hs包被支架相比,2周后hs包被的植入物增加了血管生成,有助于SMC存活和生长的增加。HS的血管生成作用可用于工程肠平滑肌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Collagen and heparan sulfate coatings differentially alter cell proliferation and attachment in vitro and in vivo.
Tissue engineering is an innovative field of research applied to treat intestinal diseases. Engineered smooth muscle requires dense smooth muscle tissue and robust vascularization to support contraction. The purpose of this study was to use heparan sulfate (HS) and collagen coatings to increase the attachment of smooth muscle cells (SMCs) to scaffolds and improve their survival after implantation. SMCs grown on biologically coated scaffolds were evaluated for maturity and cell numbers after 2, 4 and 6 weeks in vitro and both 2 and 6 weeks in vivo. Implants were also assessed for vascularization. Collagen-coated scaffolds increased attachment, growth and maturity of SMCs in culture. HS-coated implants increased angiogenesis after 2 weeks, contributing to an increase in SMC survival and growth compared to HS-coated scaffolds grown in vitro. The angiogenic effects of HS may be useful for engineering intestinal smooth muscle.
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TECHNOLOGY
TECHNOLOGY ENGINEERING, MULTIDISCIPLINARY-
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