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诱导多能干细胞在骨关节炎建模与治疗中的应用

iPSCs in Modeling and Therapy of Osteoarthritis.

作者信息

Csobonyeiova Maria, Polak Stefan, Nicodemou Andreas, Zamborsky Radoslav, Danisovic Lubos

机构信息

Institute of Histology and Embryology, Faculty of Medicine, Comenius University, Sasinkova 4, 811 08 Bratislava, Slovakia.

Institute of Medical Biology, Genetics and Clinical Genetics, Faculty of Medicine, Comenius University, Sasinkova 4, 811 08 Bratislava, Slovakia.

出版信息

Biomedicines. 2021 Feb 12;9(2):186. doi: 10.3390/biomedicines9020186.

DOI:10.3390/biomedicines9020186
PMID:33673154
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7917981/
Abstract

Osteoarthritis (OA) belongs to chronic degenerative disorders and is often a leading cause of disability in elderly patients. Typically, OA is manifested by articular cartilage erosion, pain, stiffness, and crepitus. Currently, the treatment options are limited, relying mostly on pharmacological therapy, which is often related to numerous complications. The proper management of the disease is challenging because of the poor regenerative capacity of articular cartilage. During the last decade, cell-based approaches such as implantation of autologous chondrocytes or mesenchymal stem cells (MSCs) have shown promising results. However, the mentioned techniques face their hurdles (cell harvesting, low proliferation capacity). The invention of induced pluripotent stem cells (iPSCs) has created new opportunities to increase the efficacy of the cartilage healing process. iPSCs may represent an unlimited source of chondrocytes derived from a patient's somatic cells, circumventing ethical and immunological issues. Aside from the regenerative potential of iPSCs, stem cell-derived cartilage tissue models could be a useful tool for studying the pathological process of OA. In our recent article, we reviewed the progress in chondrocyte differentiation techniques, disease modeling, and the current status of iPSC-based regenerative therapy of OA.

摘要

骨关节炎(OA)属于慢性退行性疾病,通常是老年患者致残的主要原因。典型的OA表现为关节软骨侵蚀、疼痛、僵硬和摩擦音。目前,治疗选择有限,主要依赖药物治疗,而药物治疗往往伴随着许多并发症。由于关节软骨的再生能力较差,对该疾病的妥善管理具有挑战性。在过去十年中,基于细胞的方法,如自体软骨细胞或间充质干细胞(MSCs)植入,已显示出有前景的结果。然而,上述技术面临着自身的障碍(细胞采集、增殖能力低)。诱导多能干细胞(iPSCs)的发明为提高软骨愈合过程的疗效创造了新机会。iPSCs可能代表了一种源自患者体细胞的无限软骨细胞来源,规避了伦理和免疫问题。除了iPSCs的再生潜力外,干细胞衍生的软骨组织模型可能是研究OA病理过程的有用工具。在我们最近的文章中,我们综述了软骨细胞分化技术、疾病建模以及基于iPSC的OA再生治疗的现状方面的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e2/7917981/299160bb5aa3/biomedicines-09-00186-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e2/7917981/299160bb5aa3/biomedicines-09-00186-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e2/7917981/299160bb5aa3/biomedicines-09-00186-g001.jpg

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Integration of Transcriptome and MicroRNA Profile Analysis of iMSCs Defines Their Rejuvenated State and Conveys Them into a Novel Resource for Cell Therapy in Osteoarthritis.iMSCs 转录组和 microRNA 谱分析的整合定义了它们的年轻化状态,并将其转化为骨关节炎细胞治疗的新资源。
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