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Differentiating human pluripotent stem cells into vascular smooth muscle cells in three dimensional thermoreversible hydrogels

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机构: [a]Department of Chemical and Biomolecular Engineering, University of Nebraska-Lincoln, Nebraska, USA [b]Department of Biological Systems Engineering, University of Nebraska-Lincoln, Nebraska, USA [c]Biomedical Engineering Program, University of Nebraska-Lincoln, Nebraska, USA [d]Department of Vascular Surgery, Beijing Anzhen Hospital of Capital Medical University, Beijing Institute of Heart Lung and Blood Vessel Diseases, Beijing, China [e]Department of Nutrition and Health Sciences, University of Nebraska-Lincoln, Lincoln, NE, USA [f]Mary and Dick Holland Regenerative Medicine Program, University of Nebraska Medical Center, Omaha, Nebraska, USA [g]Fred & Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, Nebraska, USA
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Vascular smooth muscle cells (VSMCs) are of great value and are needed in large quantities for tissue engineering, drug screening, disease modeling and cell-based therapies. However, getting high quantity VSMCs remains a challenge. Here, we report a method for the scalable manufacturing of VSMCs from human pluripotent stem cells (hPSCs). hPSCs are expanded and differentiated into VSMCs in a three dimensional (3D) thermoreversible hydrogel. The hydrogel not only acts as a 3D scaffold for cells to grow, but also protects cells from hydrodynamic stresses in the culture vessel and prevents cells from excessive aggregation. Together, the hydrogel creates a cell-friendly microenvironment, leading to high culture efficiency. We show that VSMCs can be generated in 10 days with high viability (>90%), high purity (>80%) and high yield (approximate to 2.0 x 10(7) cells per mL hydrogel) in the hydrogel scaffold. The generated VSMCs have normal functions. Genome-wide gene expression analysis shows VSMCs made in the hydrogel (i.e. 3D-VSMCs) have higher expression of genes related to vasculature development and glycolysis compared to VSMCs made in the conventional 2D cultures (i.e. 2D-VSMCs), while 2D-VSMCs have higher expression of genes related to cell proliferation. This simple, defined and efficient method is scalable for manufacturing hPSC-VSMCs for various biomedical applications.

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出版当年[2018]版:
大类 | 2 区 工程技术
小类 | 2 区 材料科学:生物材料
最新[2023]版:
大类 | 3 区 医学
小类 | 3 区 材料科学:生物材料
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出版当年[2017]版:
Q1 MATERIALS SCIENCE, BIOMATERIALS
最新[2023]版:
Q1 MATERIALS SCIENCE, BIOMATERIALS

影响因子: 最新[2023版] 最新五年平均 出版当年[2017版] 出版当年五年平均 出版前一年[2016版] 出版后一年[2018版]

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第一作者机构: [a]Department of Chemical and Biomolecular Engineering, University of Nebraska-Lincoln, Nebraska, USA
通讯作者:
通讯机构: [a]Department of Chemical and Biomolecular Engineering, University of Nebraska-Lincoln, Nebraska, USA [b]Department of Biological Systems Engineering, University of Nebraska-Lincoln, Nebraska, USA [f]Mary and Dick Holland Regenerative Medicine Program, University of Nebraska Medical Center, Omaha, Nebraska, USA [g]Fred & Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, Nebraska, USA
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