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用于软组织工程的甲基丙烯酸化明胶/透明质酸基水凝胶。

Methacrylated gelatin/hyaluronan-based hydrogels for soft tissue engineering.

作者信息

Kessler Lukas, Gehrke Sandra, Winnefeld Marc, Huber Birgit, Hoch Eva, Walter Torsten, Wyrwa Ralf, Schnabelrauch Matthias, Schmidt Malte, Kückelhaus Maximilian, Lehnhardt Marcus, Hirsch Tobias, Jacobsen Frank

机构信息

Department of Plastic Surgery and Burn Centre, BG University Hospital Bergmannsheil GmbH, Ruhr University Bochum, Bochum, Germany.

Research and Development, Beiersdorf AG, Hamburg, Germany.

出版信息

J Tissue Eng. 2017 Dec 21;8:2041731417744157. doi: 10.1177/2041731417744157. eCollection 2017 Jan-Dec.

Abstract

In vitro-generated soft tissue could provide alternate therapies for soft tissue defects. The aim of this study was to evaluate methacrylated gelatin/hyaluronan as scaffolds for soft tissue engineering and their interaction with human adipose-derived stem cells (hASCs). ASCs were incorporated into methacrylated gelatin/hyaluronan hydrogels. The gels were photocrosslinked with a lithium phenyl-2,4,6-trimethylbenzoylphosphinate photoinitiator and analyzed for cell viability and adipogenic differentiation of ASCs over a period of 30 days. Additionally, an angiogenesis assay was performed to assess their angiogenic potential. After 24 h, ASCs showed increased viability on composite hydrogels. These results were consistent over 21 days of culture. By induction of adipogenic differentiation, the mature adipocytes were observed after 7 days of culture, their number significantly increased until day 28 as well as expression of fatty acid binding protein 4 and adiponectin. Our scaffolds are promising as building blocks for adipose tissue engineering and allowed long viability, proliferation, and differentiation of ASCs.

摘要

体外生成的软组织可为软组织缺损提供替代疗法。本研究的目的是评估甲基丙烯酸化明胶/透明质酸作为软组织工程支架及其与人类脂肪来源干细胞(hASC)的相互作用。将脂肪来源干细胞整合到甲基丙烯酸化明胶/透明质酸水凝胶中。这些凝胶用苯基-2,4,6-三甲基苯甲酰基膦酸锂光引发剂进行光交联,并在30天的时间内分析脂肪来源干细胞的细胞活力和成脂分化情况。此外,进行了血管生成试验以评估其血管生成潜力。24小时后,脂肪来源干细胞在复合水凝胶上的活力增加。这些结果在21天的培养过程中保持一致。通过诱导成脂分化,培养7天后观察到成熟脂肪细胞,其数量在第28天之前显著增加,同时脂肪酸结合蛋白4和脂联素的表达也增加。我们的支架有望作为脂肪组织工程的构建模块,并能使脂肪来源干细胞长期保持活力、增殖和分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73eb/5753891/ec846dc0fafa/10.1177_2041731417744157-fig1.jpg

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