Suppr超能文献

研究组织特异性细胞外基质对复合水凝胶支架内人脂肪来源基质细胞成脂和成骨分化的影响。

Investigating the Effects of Tissue-Specific Extracellular Matrix on the Adipogenic and Osteogenic Differentiation of Human Adipose-Derived Stromal Cells Within Composite Hydrogel Scaffolds.

作者信息

Shridhar Arthi, Amsden Brian G, Gillies Elizabeth R, Flynn Lauren E

机构信息

Department of Chemical and Biochemical Engineering, Thompson Engineering Building, The University of Western Ontario, London, ON, Canada.

Bone and Joint Institute, The University of Western Ontario, London, ON, Canada.

出版信息

Front Bioeng Biotechnol. 2019 Dec 11;7:402. doi: 10.3389/fbioe.2019.00402. eCollection 2019.

Abstract

While it has been postulated that tissue-specific bioscaffolds derived from the extracellular matrix (ECM) can direct stem cell differentiation, systematic comparisons of multiple ECM sources are needed to more fully assess the benefits of incorporating tissue-specific ECM in stem cell culture and delivery platforms. To probe the effects of ECM sourced from decellularized adipose tissue (DAT) or decellularized trabecular bone (DTB) on the adipogenic and osteogenic differentiation of human adipose-derived stem/stromal cells (ASCs), a novel detergent-free decellularization protocol was developed for bovine trabecular bone that complemented our established detergent-free decellularization protocol for human adipose tissue and did not require specialized equipment or prolonged incubation times. Immunohistochemical and biochemical characterization revealed enhanced sulphated glycosaminoglycan content in the DTB, while the DAT contained higher levels of collagen IV, collagen VI and laminin. To generate platforms with similar structural and biomechanical properties to enable assessment of the compositional effects of the ECM on ASC differentiation, micronized DAT and DTB were encapsulated with human ASCs within methacrylated chondroitin sulfate (MCS) hydrogels through UV-initiated crosslinking. High ASC viability (>90%) was observed over 14 days in culture. Adipogenic differentiation was enhanced in the MCS+DAT composites relative to the MCS+DTB composites and MCS controls after 14 days of culture in adipogenic medium. Osteogenic differentiation studies revealed a peak in alkaline phosphatase (ALP) enzyme activity at 7 days in the MCS+DTB group cultured in osteogenic medium, suggesting that the DTB had bioactive effects on osteogenic protein expression. Overall, the current study suggests that tissue-specific ECM sourced from DAT or DTB can act synergistically with soluble differentiation factors to enhance the lineage-specific differentiation of human ASCs within 3-D hydrogel systems.

摘要

虽然有人推测,源自细胞外基质(ECM)的组织特异性生物支架可以引导干细胞分化,但需要对多种ECM来源进行系统比较,以更全面地评估在干细胞培养和递送平台中加入组织特异性ECM的益处。为了探究源自脱细胞脂肪组织(DAT)或脱细胞小梁骨(DTB)的ECM对人脂肪来源的干/基质细胞(ASC)成脂和成骨分化的影响,我们开发了一种用于牛小梁骨的新型无洗涤剂脱细胞方案,该方案补充了我们已建立的用于人脂肪组织的无洗涤剂脱细胞方案,且不需要专门设备或延长孵育时间。免疫组织化学和生化特征显示,DTB中硫酸化糖胺聚糖含量增加,而DAT中IV型胶原、VI型胶原和层粘连蛋白水平更高。为了生成具有相似结构和生物力学特性的平台,以便评估ECM组成对ASC分化的影响,通过紫外线引发交联,将微粉化的DAT和DTB与人ASC封装在甲基丙烯酸化硫酸软骨素(MCS)水凝胶中。在培养14天期间观察到ASC活力较高(>90%)。在成脂培养基中培养14天后,相对于MCS+DTB复合材料和MCS对照,MCS+DAT复合材料中的成脂分化增强。成骨分化研究显示,在成骨培养基中培养的MCS+DTB组中,碱性磷酸酶(ALP)酶活性在7天时达到峰值,表明DTB对成骨蛋白表达具有生物活性作用。总体而言,当前研究表明,源自DAT或DTB的组织特异性ECM可以与可溶性分化因子协同作用,以增强人ASC在三维水凝胶系统中的谱系特异性分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/337f/6917659/c83ae8b28541/fbioe-07-00402-g0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验