首页> 外文期刊>International journal of molecular medicine >The Wnt5a/Ror2 pathway is associated with determination of the differentiation fate of bone marrow mesenchymal stem cells in vascular calcification
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The Wnt5a/Ror2 pathway is associated with determination of the differentiation fate of bone marrow mesenchymal stem cells in vascular calcification

机译:Wnt5a / Ror2通路与确定血管钙化中骨髓间充质干细胞的分化命运有关

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Accumulating evidence have demonstrated that mesenchymal stem cells (MSCs) are involved in the initiation and progression of various vascular diseases. Canonical Wnt signaling controls the fate of MSCs, and plays an important role in vascular calcification. However, vascular calcification can be inhibited by the non-canonical Wnt signaling pathway Wnt5a/Ror2. This study aimed to investigate whether the Wnt5a/Ror2 pathway is associated with determination of the differentiation fate of MSCs in vascular calcification. Direct co-cultures were established by seeding smooth muscle cells (SMCs) or calci-fied SMCs and MSCs together at ratios of SMCs or calcified SMCs 15×104; SMCs or calcified SMCs 5×104: MSCs 10×104, SMCs or calcified SMCs 10×104: MSCs 5×104. Osteosynthesis-inducing medium (OS) was added to the culture medium in the groups of MSCs with non-calcified SMCs. Cells were cultured for nine days. Osteoblastic differentiation was evaluated by cell morphology and the activity of alkaline phosphatase (ALP) in cell lysates and ALP staining. Furthermore, we investi-gated the inhibition of Wnt signaling, and observed that the members of the non-canonical signaling pathway Wnt5a/Ror2 were expressed in each group. Additionally, MSCs cultured in culture media with OS did not differentiate into an osteoblast phenotype when in direct contact with non-calcified SMCs, irrespective of the number of MSCs. However, an osteoblast phenotype was observed when MSCs were cultured in media without OS differentiation towards direct contact with calci-fied SMCs, and the levels of osteoblastic markers had a direct correlation with the number of MSCs. Of note, the Wnt5a protein was associated with the levels of calcification, thus, although rarely detected in non-calcification, Ror2 mRNA in the non-calcified groups was significantly higher compared to that in the calcified groups. Therefore, the Wnt5a/Ror2 pathway is associated with determination of the differentia-tion fate of bone marrow mesenchymal stem cells in vascular calcification.
机译:越来越多的证据表明,间充质干细胞(MSCs)参与各种血管疾病的发生和发展。规范的Wnt信号控制MSC的命运,并在血管钙化中起重要作用。但是,非典型的Wnt信号通路Wnt5a / Ror2可以抑制血管钙化。这项研究旨在调查Wnt5a / Ror2通路是否与确定血管钙化中MSC的分化命运有关。通过将平滑肌细胞(SMC)或钙化的SMC和MSC以SMC或钙化的SMC的比例15×104接种在一起建立直接共培养。 SMC或钙化SMC 5×104:MSC 10×104,SMC或钙化SMC 10×104:MSC 5×104。将骨合成诱导培养基(OS)添加到具有非钙化SMC的MSC组的培养基中。细胞培养9天。通过细胞形态和细胞裂解液中碱性磷酸酶(ALP)的活性以及ALP染色评估成骨细胞的分化。此外,我们研究了Wnt信号转导的抑制作用,并观察到非经典信号转导途径Wnt5a / Ror2的成员在每组中均有表达。另外,与非钙化SMC直接接触时,在具有OS的培养基中培养的MSC不区分成骨细胞表型,而与MSC的数量无关。然而,当在无OS分化的培养基中培养MSC时,观察到成骨细胞表型,而没有OS分化为直接与钙化SMC接触,并且成骨细胞标志物的水平与MSC的数量直接相关。值得注意的是,Wnt5a蛋白与钙化水平有关,因此,尽管在非钙化中很少检测到,但非钙化组的Ror2 mRNA明显高于钙化组。因此,Wnt5a / Ror2途径与确定血管钙化中骨髓间充质干细胞的分化命运有关。

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