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利用髌下脂肪垫来源间充质干细胞治疗退行性关节炎的潜力:软骨生成、外泌体和转录调控。

Potential of Using Infrapatellar-Fat-Pad-Derived Mesenchymal Stem Cells for Therapy in Degenerative Arthritis: Chondrogenesis, Exosomes, and Transcription Regulation.

机构信息

Department of Orthopedic Surgery, Far Eastern Memorial Hospital, New Taipei City 220216, Taiwan.

Graduate School of Biotechnology and Bioengineering, Yuan Ze University, Taoyuan City 320315, Taiwan.

出版信息

Biomolecules. 2022 Mar 1;12(3):386. doi: 10.3390/biom12030386.

Abstract

Infrapatellar fat pad-derived mesenchymal stem cells (IPFP-MSCs) are a type of adipose-derived stem cell (ADSC). They potentially contribute to cartilage regeneration and modulation of the immune microenvironment in patients with osteoarthritis (OA). The ability of IPFP-MSCs to increase chondrogenic capacity has been reported to be greater, less age dependent, and less affected by inflammatory changes than that of other MSCs. Transcription-regulatory factors strictly regulate the cartilage differentiation of MSCs. However, few studies have explored the effect of transcriptional factors on IPFP-MSC-based neocartilage formation, cartilage engineering, and tissue functionality during and after chondrogenesis. Instead of intact MSCs, MSC-derived extracellular vesicles could be used for the treatment of OA. Furthermore, exosomes are increasingly being considered the principal therapeutic agent in MSC secretions that is responsible for the regenerative and immunomodulatory functions of MSCs in cartilage repair. The present study provides an overview of advancements in enhancement strategies for IPFP-MSC chondrogenic differentiation, including the effects of transcriptional factors, the modulation of released exosomes, delivery mechanisms for MSCs, and ethical and regulatory points concerning the development of MSC products. This review will contribute to the understanding of the IPFP-MSC chondrogenic differentiation process and enable the improvement of IPFP-MSC-based cartilage tissue engineering.

摘要

髌下脂肪垫来源间充质干细胞(IPFP-MSCs)是一种脂肪来源的干细胞(ADSC)。它们可能有助于骨关节炎(OA)患者的软骨再生和免疫微环境的调节。与其他间充质干细胞相比,IPFP-MSCs 增加软骨生成能力的能力被报道具有更大、更少年龄依赖性和更少受炎症变化影响的特点。转录调节因子严格调节间充质干细胞的软骨分化。然而,很少有研究探讨转录因子对基于 IPFP-MSC 的新软骨形成、软骨工程和软骨内成骨过程中和之后的组织功能的影响。替代完整的间充质干细胞,MSC 衍生的细胞外囊泡可用于 OA 的治疗。此外,外泌体越来越被认为是 MSC 分泌中负责 MSC 在软骨修复中的再生和免疫调节功能的主要治疗剂。本研究概述了增强 IPFP-MSC 软骨分化的增强策略的进展,包括转录因子的影响、释放的外泌体的调节、MSC 的递送机制以及 MSC 产品开发的伦理和监管要点。这篇综述将有助于理解 IPFP-MSC 的软骨分化过程,并能够改进基于 IPFP-MSC 的软骨组织工程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efdc/8945217/14207f736a91/biomolecules-12-00386-g001.jpg

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