State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Department of Stomatology, Medical College, Dalian University, Dalian, 116622, Liaoning, China.
Curr Stem Cell Res Ther. 2024;19(7):1029-1041. doi: 10.2174/011574888X260686231023091127.
Stem cell properties vary considerably based on the source and tissue site of mesenchymal stem cells (MSCs). The mandibular condyle is a unique kind of craniofacial bone with a special structure and a relatively high remodeling rate. MSCs here may also be unique to address specific physical needs.
The aim of this study was to compare the proliferation and multidirectional differentiation potential among MSCs derived from the tibia (TMSCs), mandibular ramus marrow (MMSCs), and condylar subchondral bone (SMSCs) of rats .
Cell proliferation and migration were assessed by CCK-8, laser confocal, and cell scratch assays. Histochemical staining and real-time PCR were used to evaluate the multidirectional differentiation potential and DNA methylation and histone deacetylation levels.
The proliferation rate and self-renewal capacity of SMSCs were significantly higher than those of MMSCs and TMSCs. Moreover, SMSCs possessed significantly higher mineralization and osteogenic differentiation potential. and may be instrumental in the osteogenesis of SMSCs. In addition, SMSCs are distinct from MMSCs and TMSCs with lower adipogenic differentiation and chondrogenic differentiation potential. The multidirectional differentiation capacities of TMSCs were exactly the opposite of those of SMSCs, and the results of MMSCs were intermediate.
This research offers a new paradigm in which SMSCs could be a useful source of stem cells for further application in stem cell-based medical therapies due to their strong cell renewal and osteogenic capacity.
间充质干细胞(MSCs)的来源和组织部位不同,其干细胞特性差异很大。下颌骨髁突是一种独特的颅面骨,具有特殊的结构和相对较高的改建率。这里的 MSCs 也可能具有独特性,以满足特定的物理需求。
本研究旨在比较来源于大鼠胫骨(TMSCs)、下颌支骨髓(MMSCs)和髁突软骨下骨(SMSCs)的 MSCs 的增殖和多向分化潜能。
通过 CCK-8、激光共聚焦和细胞划痕实验评估细胞增殖和迁移。组织化学染色和实时 PCR 用于评估多向分化潜能以及 DNA 甲基化和组蛋白去乙酰化水平。
SMSCs 的增殖率和自我更新能力明显高于 MMSCs 和 TMSCs。此外,SMSCs 具有更高的矿化和成骨分化潜能。DNA 甲基化和组蛋白去乙酰化可能有助于 SMSCs 的成骨作用。此外,SMSCs 与 MMSCs 和 TMSCs 不同,其脂肪和成软骨分化潜能较低。TMSCs 的多向分化能力与 SMSCs 相反,而 MMSCs 的结果则处于中间。
由于 SMSCs 具有较强的细胞更新和成骨能力,因此本研究为进一步将 SMSCs 应用于基于干细胞的医学治疗提供了一个新的范例。