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使用生物流体和自体来源的间充质干细胞的诱导性软骨生成纳米纤维基质。

Chondrogenesis-inductive nanofibrous substrate using both biological fluids and mesenchymal stem cells from an autologous source.

机构信息

3B's Research Group, I3Bs - Research Institute on Biomaterials, Biodegradables and Biomimetics of University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark - Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Barco/Guimarães, Portugal; ICVS/3B's - PT Government Associate Laboratory, Braga/Guimarães 4805-017, Portugal.

3B's Research Group, I3Bs - Research Institute on Biomaterials, Biodegradables and Biomimetics of University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark - Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Barco/Guimarães, Portugal; ICVS/3B's - PT Government Associate Laboratory, Braga/Guimarães 4805-017, Portugal; The Discoveries Centre for Regenerative and Precision Medicine, Headquarters at University of Minho, Avepark, 4805-017, Barco, Guimarães, Portugal.

出版信息

Mater Sci Eng C Mater Biol Appl. 2019 May;98:1169-1178. doi: 10.1016/j.msec.2019.01.069. Epub 2019 Jan 16.

Abstract

During the last decade, many cartilage tissue engineering strategies have been developed, being the stem cell-based approach one of the most promising. Transforming Growth Factor-β3 (TGF-β3) and Insulin-like Growth Factor-I (IGF-I) are key proteins involved in the regulation of chondrogenic differentiation. Therefore, these two growth factors (GFs) were immobilized at the surface of a single electrospun nanofibrous mesh (NFM) aiming to differentiate human Bone Marrow-derived Mesenchymal Stem Cells (hBM-MSCs). The immobilization of defined antibodies (i.e. anti-TGF-β3 and anti-IGF-I) allows the selective retrieval of the abovementioned GFs from human platelet lysates (PL). Biochemical assays, involving hBM-MSCs cultured on biofunctional nanofibrous substrates under basal culture medium during 28 days, confirm the biological activity of bound TGF-β3 and IGF-I. Specifically, the typical spherical morphology of chondrocytes and the immunolocalization of collagen type II confirmed the formation of a cartilaginous ECM. Therefore, the proposed biofunctional nanofibrous substrate is able to promote chondrogenesis.

摘要

在过去的十年中,已经开发出许多软骨组织工程策略,其中基于干细胞的方法是最有前途的方法之一。转化生长因子-β3(TGF-β3)和胰岛素样生长因子-I(IGF-I)是参与软骨分化调节的关键蛋白。因此,这两种生长因子(GFs)被固定在单个电纺纳米纤维网(NFM)的表面上,目的是分化人骨髓间充质干细胞(hBM-MSCs)。固定的定义抗体(即抗 TGF-β3 和抗 IGF-I)允许从人血小板裂解物(PL)中选择性回收上述 GFs。涉及在基础培养基中培养 28 天的生物功能纳米纤维底物上的 hBM-MSCs 的生化分析证实了结合的 TGF-β3 和 IGF-I 的生物活性。具体而言,软骨细胞的典型球形形态和 II 型胶原的免疫定位证实了软骨细胞外基质的形成。因此,所提出的生物功能纳米纤维基底能够促进软骨生成。

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