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下调热休克蛋白 70 会损害人骨髓间充质干细胞的成骨和成软骨分化。

Downregulation of Heat Shock Protein 70 Impairs Osteogenic and Chondrogenic Differentiation in Human Mesenchymal Stem Cells.

机构信息

Department of Biomedical Engineering, City University of New York-City College, 160 Convent Avenue, New York, NY, 10031, USA.

出版信息

Sci Rep. 2018 Jan 11;8(1):553. doi: 10.1038/s41598-017-18541-1.

Abstract

Human mesenchymal stem cells (hMSCs) show promise for bone and cartilage regeneration. Our previous studies demonstrated that hMSCs with periodic mild heating had enhanced osteogenic and chondrogenic differentiation with significantly upregulated heat shock protein 70 (HSP70). However, the role of HSP70 in adult tissue regeneration is not well studied. Here, we revealed an essential regulatory mechanism of HSP70 in osteogenesis and chondrogenesis using adult hMSCs stably transfected with specific shRNAs to knockdown HSP70. Periodic heating at 39 °C was applied to hMSCs for up to 26 days. HSP70 knockdown resulted in significant reductions of alkaline phosphatase activity, calcium deposition, and gene expression of Runx2 and Osterix during osteogenesis. In addition, knockdown of HSP70 led to significant decreases of collagens II and X during chondrogenesis. Thus, downregulation of HSP70 impaired hMSC osteogenic and chondrogenic differentiation as well as the enhancement of these processes by thermal treatment. Taken together, these findings suggest a putative mechanism of thermal-enhanced bone and cartilage formation and underscore the importance of HSP70 in adult bone and cartilage differentiation.

摘要

人骨髓间充质干细胞(hMSCs)在骨和软骨再生方面显示出巨大的潜力。我们之前的研究表明,周期性轻度加热的 hMSCs 具有增强的成骨和成软骨分化能力,其热休克蛋白 70(HSP70)显著上调。然而,HSP70 在成人组织再生中的作用尚未得到充分研究。在这里,我们使用特异性 shRNA 稳定转染的成年 hMSCs 揭示了 HSP70 在成骨和成软骨中的重要调节机制。将 hMSCs 加热至 39°C 长达 26 天。在成骨过程中,HSP70 的敲低导致碱性磷酸酶活性、钙沉积以及 Runx2 和 Osterix 的基因表达显著降低。此外,HSP70 的敲低导致软骨形成过程中 II 型和 X 型胶原显著减少。因此,HSP70 的下调会损害 hMSC 的成骨和成软骨分化,以及热治疗对这些过程的增强。总之,这些发现表明了热增强骨和软骨形成的一种可能机制,并强调了 HSP70 在成人骨和软骨分化中的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea48/5765044/0bcda4206d03/41598_2017_18541_Fig1_HTML.jpg

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