Autoclavable Polydopamine-Gelatin-Modified Polyethylene Terephthalate Microfibrous Carriers Regulate the Proliferation and Paracrine Signaling of Mesenchymal Stem Cells

间充质干细胞 旁分泌信号 明胶 聚对苯二甲酸乙二醇酯 细胞生物学 材料科学 细胞粘附 体外 细胞生长 细胞培养 粘附 生物物理学 生物医学工程 化学 医学 生物 生物化学 受体 复合材料 遗传学
作者
Hao Ye,Yan Li,Jinze Li,Cong Cao,Yuxi Luo,Yihong Gong
出处
期刊:ACS applied polymer materials [American Chemical Society]
卷期号:4 (5): 3711-3725 被引量:1
标识
DOI:10.1021/acsapm.2c00232
摘要

Mesenchymal stem cells (MSCs) have attracted considerable attention in cell therapies and tissue engineering for their multilineage differentiation potential and immunomodulatory properties. However, MSCs gradually lose their stemness and multipotentiality in prolonged two-dimensional (2D) culture in vitro. Herein, a three-dimensional (3D) polyethylene terephthalate (PET) microfiber sponge served as the substrate, and gelatin macromolecules were grafted onto PET through the adsorption of polydopamine to prepare a 3D cell carrier (PET-Gel) with an interpenetrating network structure. The cell carrier could be sterilized by autoclaving. The material characterization results showed that the 3D carrier had good coating stability, thermal stability, and mechanical properties; these properties did not decrease after autoclaving. In vitro cell experiments revealed that the 3D cell carrier promoted the adhesion and proliferation of human umbilical cord MSCs (HUCMSCs). In long-term culture (2 weeks), the cell proliferation rate was 2.4-fold higher than that on 2D plates because the interpenetrating network structure of the carrier led to a larger growing area than 2D plates and the cells infiltrated into the interior of the carrier. Simultaneously, HUCMSCs on PET-Gel expressed surface-specific antigens of the MSCs. The typical paracrine cytokine expression was characterized using qPCR and Western blotting. The paracrine function of cells on the 3D carrier was nearly equivalent to that on the 2D plates. These results showed that the PET-Gel carrier was suitable for the long-term culture of HUCMSCs in vitro.
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