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利用患者来源的诱导多能干细胞对早发性手指骨关节炎样病症进行表征。

Characterization of Early-Onset Finger Osteoarthritis-Like Condition Using Patient-Derived Induced Pluripotent Stem Cells.

机构信息

Catholic iPSC Research Center, College of Medicine, The Catholic University of Korea, Seoul 06591, Korea.

Department of Internal Medicine, Division of Rheumatology, Institute of Medical Science, College of Medicine, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul 06591, Korea.

出版信息

Cells. 2021 Feb 4;10(2):317. doi: 10.3390/cells10020317.

Abstract

Early osteoarthritis (OA)-like symptoms are difficult to study owing to the lack of disease samples and animal models. In this study, we generated induced pluripotent stem cell (iPSC) lines from a patient with a radiographic early-onset finger osteoarthritis (efOA)-like condition in the distal interphalangeal joint and her healthy sibling. We differentiated those cells with similar genetic backgrounds into chondrogenic pellets (CPs) to confirm efOA. CPs generated from efOA-hiPSCs (efOA-CPs) showed lower levels of , which is a key marker of hyaline cartilage after complete differentiation, for 21 days. Increase in pellet size and vacuole-like morphologies within the pellets were observed in the efOA-CPs. To analyze the changes occurred during the development of vacuole-like morphology and the increase in pellet size in efOA-CPs, we analyzed the expression of OA-related markers on day 7 of differentiation and showed an increase in the levels of , , , and in efOA-CPs. IL-6, MMP1, and MMP10 levels were also increased in the efOA-CPs. Taken together, we present proof-of-concept regarding disease modeling of a unique patient who showed OA-like symptoms.

摘要

由于缺乏疾病样本和动物模型,早期骨关节炎 (OA) 样症状难以研究。在这项研究中,我们从一位影像学早期指间关节手指骨关节炎 (efOA) 样疾病患者及其健康的兄弟姐妹中生成了诱导多能干细胞 (iPSC) 系。我们将这些具有相似遗传背景的细胞分化为软骨形成的球体 (CPs) 以确认 efOA。来自 efOA-iPSC (efOA-CPs) 的 CPs 在完全分化后的 21 天内显示出较低水平的, 这是透明软骨的关键标志物。在 efOA-CPs 中观察到球体大小增加和球体内部出现空泡样形态。为了分析 efOA-CPs 中空泡样形态发育和球体大小增加过程中发生的变化,我们在分化第 7 天分析了与 OA 相关的标志物的表达,并显示 efOA-CPs 中的,,, 和 水平增加。IL-6、MMP1 和 MMP10 水平在 efOA-CPs 中也增加。综上所述,我们提供了一个独特的患者 OA 样症状疾病模型的概念验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24cb/7913990/6f02fb3297dc/cells-10-00317-g001.jpg

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