Subchondral bone derived mesenchymal stem cells display enhanced osteo-chondrogenic differentiation, self-renewal and proliferation potentials.

Subchondral bone derived mesenchymal stem cells display enhanced osteo-chondrogenic differentiation, self-renewal and proliferation potentials.
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软骨下骨来源的间充质干细胞表现出增强的骨软骨分化、自我更新和增殖潜力。

DOI:
10.1538/expanim.17-0137
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发表时间:
2018-07-30
影响因子:
2.4
通讯作者:
Zhu H
Zhu H
中科院分区:
医学4区
文献类型:
--
作者:
Zhang H;Li ZL;Su XZ;Ding L;Li J;Zhu H

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兔骨髓间充质干细胞(MSCs)是再生医学研究,特别是转化研究的重要种子细胞。在目前的研究中,我们发现兔软骨下骨是一种可靠的MSCs来源。首先,我们从兔膝关节获取软骨下骨(SCB),通过培养酶处理的SCB来启动MSC培养。从SCB生长出来的贴壁成纤维细胞样细胞满足用于定义MSC的常见免疫表型标准,但具有低污染的CD 45+造血细胞。有趣的是,分化的SCB-MSC表达的成骨和成软骨标志物水平显着高于骨髓细胞悬液来源的MSC(BMS-MSC)(P<0.05)。SCB-MSC和BMS-MSC成脂标志物的表达差异无统计学意义(P>0.05)。殖民地集落形成单位-成纤维细胞实验和成球实验结果表明,SCB-MSCs具有较强的自我更新能力。SCB-MSCs的干性标志物Nanog、OCT 4和Sox-2的表达水平高于BMS-MSCs(P<0.05)。CCK-8法和CFSE法结果均显示SCB-MSCs具有较强的增殖能力。此外,SCB-MSCs表现出更高的细胞外信号相关激酶/丝裂原活化蛋白激酶信号的磷酸化,这与MSC增殖密切相关。总之,我们确定SCB-MSC作为一种新的干细胞群体,满足MSC的要求; SCB-MSC的独特性质是重要的潜在治疗疾病和创伤引起的组织损伤。
Rabbit mesenchymal stem cells (MSCs) are important seed cells in regenerative medicine research, particularly in translational research. In the current study, we showed that rabbit subchondral bone is a reliable source of MSCs. First, we harvested subchondral bone (SCB) from the rabbit knee-joint and initiated the MSC culture by cultivating enzyme-treated SCB. Adherent fibroblast-like cells that outgrew from SCB fulfill the common immuno-phenotypic criteria for defining MSCs, but with low contamination of CD45+ hematopoietic cells. Interestingly, differentiated SCB-MSCs expressed osteogenic and chondrogenic markers at significantly higher levels than those in bone marrow cell suspension-derived MSCs (BMS-MSCs) (P<0.05). No differences in the expression of adipogenic markers between SCB-MSC and BMS-MSC (P>0.05) were observed. Moreover, the results of the colony forming unit-fibroblast assay and sphere formation assay demonstrated that the SCB-MSCs had increased self-renewal potential. SCB-MSCs expressed higher levels of the stemness markers Nanog, OCT4, and Sox-2 compared to in BMS-MSCs (P<0.05). Furthermore, the results of both the CCK-8-based assay and CFSE dilution assay showed that SCB-MSCs exhibited enhanced proliferative capacity. In addition, SCB-MSCs exhibited higher phosphorylation of extracellular signal-related kinase/mitogen-activated protein kinase signaling, which is closely related to MSC proliferation. In conclusion, we identified SCB-MSCs as a novel stem cell population that met the requirements of MSCs; the unique properties of SCB-MSC are important for the potential treatment of tissue damage resulting from disease and trauma.
DOI: 10.4155/fsoa-2017-0055
发表时间: 2017-11
期刊: Future science OA
影响因子: 2.5
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