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纤维蛋白支架可促进人脂肪来源干细胞向心肌样细胞分化过程中的存活。

Fibrin scaffold could promote survival of the human adipose-derived stem cells during differentiation into cardiomyocyte-like cells.

机构信息

Department of Clinical Biochemistry, Faculty of Medical Sciences, Tarbiat Modares University, P. O. Box: 14115-111, Tehran, Iran.

Department of Anatomy, Afzalipour School of Medicine and Physiology Research Center, Institute of Basic and Clinical Physiology Sciences, Kerman University of Medical Sciences, Kerman, Iran.

出版信息

Cell Tissue Res. 2018 Jun;372(3):571-589. doi: 10.1007/s00441-018-2799-9. Epub 2018 Mar 6.

Abstract

Human adipose-derived stem cells (hADSCs) are capable of differentiation into many cells including cardiac cells. Different types of scaffolds are used for cell differentiation but the best is yet to be determined. In this study, fibrin scaffold (3D) was fabricated using human plasma fibrinogen and compared with culture plates (2D) for the growth and differentiation of hADSCs into cardiomyocyte-like cells. For this purpose, after obtaining the properties of the isolated hADSCs and fibrin scaffold, four biochemical tests were employed to determine the relative growth rate of hADSCs in 2D and 3D cultures. To examine the effects of two different culture systems on cardiomyogenic differentiation, hADSCs were treated with 10 or 50 μM 5-azacytidine (5-Aza) for 24 h and followed until 10 weeks. The results indicated that the growth of hADSCs in 3D significantly increased after the seventh day (P < 0.05). Western blot, qRT-PCR and immunochemistry assays were used to evaluate the rate of cardiac differentiation, which showed significantly higher expression of special cardiac genes such as NKX2.5, Cx43, MLC2v, βMHC, HAND1, HAND2 and cTnI (P < 0.05) in the treated hADSCs with 50 μM 5-Aza in the 3D group. However, the expression level of the specific cardiac proteins in 3D was not significant using western blot and immunofluorescence staining. In conclusion, this study suggests that the fibrin scaffold with a compressive stress of 107.74 kPa can keep the cells alive for 10 weeks and also allows a higher and sooner differentiation of hADSCs into cardiomyocyte-like cells treated with 50 μM 5-Aza.

摘要

人脂肪干细胞(hADSCs)能够分化为多种细胞,包括心肌细胞。不同类型的支架用于细胞分化,但最好的尚未确定。在这项研究中,使用人血浆纤维蛋白原制备了纤维蛋白支架(3D),并将其与培养板(2D)进行了比较,以研究 hADSCs 向心肌细胞样细胞的生长和分化。为此,在获得分离的 hADSCs 和纤维蛋白支架的特性后,使用了四种生化测试来确定 hADSCs 在 2D 和 3D 培养中的相对生长率。为了研究两种不同培养系统对心肌生成分化的影响,用 10 或 50μM 5-氮杂胞苷(5-Aza)处理 hADSCs 24 小时,然后继续培养 10 周。结果表明,hADSCs 在第 7 天(P<0.05)后在 3D 中的生长显著增加。使用 Western blot、qRT-PCR 和免疫化学测定来评估心脏分化率,结果显示在 3D 组中用 50μM 5-Aza 处理的 hADSCs 中,特殊心脏基因如 NKX2.5、Cx43、MLC2v、βMHC、HAND1、HAND2 和 cTnI 的表达显著升高(P<0.05)。然而,在 3D 中使用 Western blot 和免疫荧光染色,特殊心脏蛋白的表达水平没有显著差异。总之,本研究表明,具有 107.74kPa 压缩应力的纤维蛋白支架可以使细胞存活 10 周,并且还允许用 50μM 5-Aza 处理的 hADSCs 更快、更早地分化为心肌细胞样细胞。

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