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Osteodifferentiated Mesenchymal Stem Cells from Bone Marrow and Adipose Tissue Express HLA-G and Display Immunomodulatory Properties in HLA-Mismatched Settings: Implications in Bone Repair Therapy

机译:骨髓和脂肪组织的骨分化间充质干细胞表达HLA-G并在HLA不匹配的环境中显示免疫调节特性:对骨修复治疗的意义

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摘要

Mesenchymal stem cells (MSCs) are multipotent cells that can be obtained from several sources such as bone marrow and adipose tissue. Depending on the culture conditions, they can differentiate into osteoblasts, chondroblasts, adipocytes, or neurons. In this regard, they constitute promising candidates for cell-based therapy aimed at repairing damaged tissues. In addition, MSCs display immunomodulatory properties through the expression of soluble factors including HLA-G. We here analyse both immunogenicity and immunosuppressive capacity of MSCs derived from bone marrow and adipose tissue before and after osteodifferentiation. Results show that HLA-G expression is maintained after osteodifferentiation and can be boosted in inflammatory conditions mimicked by the addition of IFN-γ and TNF-α. Both MSCs and osteodifferentiated MSCs are hypoimmunogenic and exert immunomodulatory properties in HLA-mismatched settings as they suppress T cell alloproliferation in mixed lymphocyte reactions. Finally, addition of biomaterials that stimulate bone tissue formation did not modify MSC immune properties. As MSCs combine both abilities of osteoregeneration and immunomodulation, they may be considered as allogenic sources for the treatment of bone defects.
机译:间充质干细胞(MSC)是多能细胞,可以从多种来源获得,例如骨髓和脂肪组织。根据培养条件,它们可以分化为成骨细胞,成软骨细胞,脂肪细胞或神经元。在这方面,它们构成了旨在修复受损组织的基于细胞的疗法的有希望的候选者。另外,MSC通过包括HLA-G在内的可溶性因子的表达而显示出免疫调节特性。我们在这里分析骨髓分化前后骨髓和脂肪组织来源的MSC的免疫原性和免疫抑制能力。结果显示,在骨分化后,HLA-G表达得以维持,并且在通过添加IFN-γ和TNF-α模仿的炎症条件下可以增强。 MSC和骨分化型MSC均具有低免疫原性,并且在HLA不匹配的环境中发挥免疫调节特性,因为它们抑制混合淋巴细胞反应中的T细胞同种异体增殖。最后,添加刺激骨组织形成的生物材料不会改变MSC的免疫特性。由于MSC将骨再生和免疫调节能力结合在一起,因此它们可以被认为是治疗骨缺损的同种异体来源。

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