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Extracellular Protease Inhibition Alters the Phenotype of Chondrogenically Differentiating Human Mesenchymal Stem Cells (MSCs) in 3D Collagen Microspheres

机译:细胞外蛋白酶抑制改变3D胶原微球中软骨分化人类间充质干细胞(MSCs)的表型。

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摘要

Matrix remodeling of cells is highly regulated by proteases and their inhibitors. Nevertheless, how would the chondrogenesis of mesenchymal stem cells (MSCs) be affected, when the balance of the matrix remodeling is disturbed by inhibiting matrix proteases, is incompletely known. Using a previously developed collagen microencapsulation platform, we investigated whether exposing chondrogenically differentiating MSCs to intracellular and extracellular protease inhibitors will affect the extracellular matrix remodeling and hence the outcomes of chondrogenesis. Results showed that inhibition of matrix proteases particularly the extracellular ones favors the phenotype of fibrocartilage rather than hyaline cartilage in chondrogenically differentiating hMSCs by upregulating type I collagen protein deposition and type II collagen gene expression without significantly altering the hypertrophic markers at gene level. This study suggests the potential of manipulating extracellular proteases to alter the outcomes of hMSC chondrogenesis, contributing to future development of differentiation protocols for fibrocartilage tissues for intervertebral disc and meniscus tissue engineering.
机译:蛋白酶及其抑制剂高度调节细胞的基质重塑。然而,当基质重塑的平衡被抑制基质蛋白酶所干扰时,如何影响间充质干细胞(MSCs)的软骨形成,这是不完全已知的。使用以前开发的胶原蛋白微囊化平台,我们调查了软骨分化的MSCs暴露于细胞内和细胞外蛋白酶抑制剂是否会影响细胞外基质重塑,进而影响软骨形成的结果。结果表明,通过上调I型胶原蛋白的沉积和II型胶原基因的表达而不显着改变基因水平的肥大标志物,抑制软骨基质的蛋白酶,特别是细胞外蛋白酶,有利于软骨分化的hMSCs的纤维软骨表型,而不是透明软骨。这项研究表明操纵细胞外蛋白酶改变hMSC软骨形成的结果的潜力,为椎间盘和半月板组织工程的纤维软骨组织分化方案的未来发展做出了贡献。

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