Mesenchymal Cells Retain the Specificity of Embryonal Origin During Osteogenic Differentiation

间充质干细胞 细胞生物学 生物 细胞分化 遗传学 基因
作者
Arseniy Lobov,Polina Kuchur,Aigul Khizhina,A. V. Kotova,Andrei Ivashkin,Daria Kostina,Polina Klausen,Evgeniia Khokhlova,Egor Repkin,Kseniia Postnikova,Daria Perepletchikova,Evgeny V. Denisov,Tatiana S. Gerashchenko,Rashid Tikhilov,С. А. Божкова,А. П. Середа,Vitaliy Karelkin,N. I. Enukashvily,Anna Malashicheva
出处
期刊:Stem Cells [Wiley]
卷期号:42 (1): 76-89 被引量:7
标识
DOI:10.1093/stmcls/sxad081
摘要

Abstract Mesenchymal stem cells (MSCs) are widely used in therapy, but the differences between MSCs of various origins and their ability to undergo osteogenic differentiation and produce extracellular matrix are not fully understood. To address this, we conducted a comparative analysis of mesenchymal cell primary cultures from 6 human sources, including osteoblast-like cells from the adult femur, adipose-derived stem cells, Wharton’s jelly-derived mesenchymal cells, gingival fibroblasts, dental pulp stem cells, and periodontal ligament stem cells. We analyzed these cells’ secretome, proteome, and transcriptome under standard and osteogenic cultivation conditions. Despite the overall similarity in osteogenic differentiation, the cells maintain their embryonic specificity after isolation and differentiation in vitro. Furthermore, we propose classifying mesenchymal cells into 3 groups: dental stem cells of neural crest origin, mesenchymal stem cells, and fetal stem cells. Specifically, fetal stem cells have the most promising secretome for various applications, while mesenchymal stem cells have a specialized secretome optimal for extracellular matrix production. Nevertheless, mesenchymal cells from all sources secreted core bone extracellular matrix-associated proteins. In conclusion, our study illuminates the distinctive characteristics of mesenchymal stem cells from various sources, providing insights into their potential applications in regenerative medicine and enhancing our understanding of the inherent diversity of mesenchymal cells in vivo.
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