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Cytokine Chemokine and Growth Factor Profile Characterization of Undifferentiated and Osteoinduced Human Adipose-Derived Stem Cells

机译:未分化和骨诱导的人类脂肪干细胞的细胞因子趋化因子和生长因子特征分析

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摘要

Bone is the second most manipulated tissue after blood. Adipose-derived stem cells (ASCs) may become a convenient source of MSC for bone regenerative protocols. Surprisingly, little is known about the most significant biomolecules these cells produce and release after being osteoinduced. Therefore, the present study aimed at dosing 13 candidates chosen among the most representative cytokines, chemokines, and growth factors within the conditioned media of osteodifferentiated and undifferentiated ASCs. Two acknowledged osteoblastic cell models, that is, MG-63 and SaOs-2 cells, were compared. Notably, IL-6, IL-8, MCP-1, and VEGF were highly produced and detectable in ASCs. In addition, while IL-6 and IL-8 seemed to be significantly induced by the osteogenic medium, no such effect was seen for MCP-1 and VEGF. Overall SaOS-2 had a poor expression profile, which may be consistent with the more differentiated phenotype of SaOs-2 compared to ASCs and MG-63. Instead, in maintaining medium, MG-63 displayed a very rich production of IL-12, MCP-1, IP-10, and VEGF, which were significantly reduced in osteogenic conditions, with the only exception of MCP-1. The high expression of MCP-1 and VEGF, even after the osteogenic commitment, may support the usage of ASCs in bone regenerative protocols by recruiting both osteoblasts and osteoclasts of the host.
机译:骨骼是仅次于血液的第二大被操纵的组织。脂肪干细胞(ASC)可能会成为骨再生协议中MSC的便捷来源。令人惊讶的是,这些细胞在骨诱导后产生和释放的最重要的生物分子知之甚少。因此,本研究旨在在骨分化和未分化ASC的条件培养基中,从最有代表性的细胞因子,趋化因子和生长因子中选择13种候选药物。比较了两个公认的成骨细胞模型,即MG-63和SaOs-2细胞。值得注意的是,IL-6,IL-8,MCP-1和VEGF在ASC中高产且可检出。另外,尽管成骨培养基似乎明显诱导了IL-6和IL-8,但对于MCP-1和VEGF却没有观察到这种作用。总体而言,SaOS-2的表达谱较差,这可能与SaSCs-2与ASC和MG-63相比具有更高的表型一致。相反,在维持培养基中,MG-63表现出非常丰富的IL-12,MCP-1,IP-10和VEGF的产生,在成骨条件下均显着降低,只有MCP-1例外。即使在成骨作用之后,MCP-1和VEGF的高表达也可能通过募集宿主的成骨细胞和破骨细胞来支持ASC在骨再生方案中的使用。

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