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
中科院分区:
文献类型:
--
作者:
Zhang H;Li ZL;Su XZ;Ding L;Li J;Zhu H
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.
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影响因子:
2.5
作者:
Ilas DC;Churchman SM;McGonagle D;Jones E
通讯作者:
Jones E
DOI:
10.1016/j.bbrc.2014.01.084
发表时间:
2014-02-28
影响因子:
3.1
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通讯作者:
Shim, Kwang Yong
影响因子:
5.2
作者:
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通讯作者:
Ritter, Thomas
DOI:
10.1016/j.injury.2010.09.027
发表时间:
2010-11-01
影响因子:
2.5
作者:
de Girolamo, Laura;Bertolini, Giulia;Volpi, Piero
通讯作者:
Volpi, Piero
影响因子:
6.2
作者:
FRIEDENSTEIN, AJ;CHAILAKHYAN, RK;KEILISSB.IV
通讯作者:
KEILISSB.IV