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控制生长因子的释放和周期性拉伸可使脂肪来源干细胞呈现平滑肌细胞样表型。

Controlled Growth Factor Delivery and Cyclic Stretch Induces a Smooth Muscle Cell-like Phenotype in Adipose-Derived Stem Cells.

机构信息

Department of Biomedical Engineering, University of Michigan, 1107 Carl A. Gerstacker Building, 2200 Bonisteel Blvd, Ann Arbor, MI 48109, USA.

G.E.R.N. Center for Tissue Replacement, Regeneration & Neogenesis, Department of Orthopedics and Trauma Surgery, Faculty of Medicine, Albert-Ludwigs-University of Freiburg, Engesserstraße 4, 79108 Freiburg, Germany.

出版信息

Cells. 2021 Nov 11;10(11):3123. doi: 10.3390/cells10113123.

Abstract

Adipose-derived stem cells (ASCs) are an abundant and easily accessible multipotent stem cell source with potential application in smooth muscle regeneration strategies. In 3D collagen hydrogels, we investigated whether sustained release of growth factors (GF) PDGF-AB and TGF-β1 from GF-loaded microspheres could induce a smooth muscle cell (SMC) phenotype in ASCs, and if the addition of uniaxial cyclic stretch could enhance the differentiation level. This study demonstrated that the combination of cyclic stretch and GF release over time from loaded microspheres potentiated the differentiation of ASCs, as quantified by protein expression of early to late SMC differentiation markers (SMA, TGLN and smooth muscle MHC). The delivery of GFs via microspheres produced large ASCs with a spindle-shaped, elongated SMC-like morphology. Cyclic strain produced the largest, longest, and most spindle-shaped cells regardless of the presence or absence of growth factors or the growth factor delivery method. Protein expression and cell morphology data confirmed that the sustained release of GFs from GF-loaded microspheres can be used to promote the differentiation of ASCs into SMCs and that the addition of uniaxial cyclic stretch significantly enhances the differentiation level, as quantified by intermediate and late SMC markers and a SMC-like elongated cell morphology.

摘要

脂肪来源干细胞(ASCs)是一种丰富且易于获取的多能干细胞来源,具有应用于平滑肌再生策略的潜力。在 3D 胶原水凝胶中,我们研究了生长因子(GF)PDGF-AB 和 TGF-β1 从负载 GF 的微球中的持续释放是否可以诱导 ASC 中的平滑肌细胞(SMC)表型,以及外加的单轴循环拉伸是否可以增强分化水平。本研究表明,循环拉伸和负载微球中 GF 随时间的释放的组合增强了 ASC 的分化,这可以通过早期至晚期 SMC 分化标志物(SMA、TGLN 和平滑肌 MHC)的蛋白表达来定量。通过微球传递 GFs 产生了具有梭形、拉长的 SMC 样形态的大型 ASC。无论是否存在生长因子或生长因子的传递方法,循环应变都会产生最大、最长和最梭形的细胞。蛋白表达和细胞形态学数据证实,从负载 GF 的微球中持续释放 GFs 可用于促进 ASC 向 SMC 的分化,并且外加的单轴循环拉伸显著增强了分化水平,这可以通过中间和晚期 SMC 标志物和 SMC 样拉长的细胞形态来定量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5cf/8624888/7eb4cc39a0f6/cells-10-03123-g001.jpg

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