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Evaluation of HLA-G Expression in Multipotent Mesenchymal Stromal Cells Derived from Vitrified Wharton’s Jelly Tissue

机译:玻璃化沃顿胶冻组织衍生的多能间充质基质细胞中HLA-G表达的评估

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摘要

Background: Mesenchymal Stromal Cells (MSCs) from Wharton’s Jelly (WJ) tissue express HLA-G, a molecule which exerts several immunological properties. This study aimed at the evaluation of HLA-G expression in MSCs derived from vitrified WJ tissue. Methods: WJ tissue samples were isolated from human umbilical cords, vitrified with the use of VS55 solution and stored for 1 year at −196 °C. After 1 year of storage, the WJ tissue was thawed and MSCs were isolated. Then, MSCs were expanded until reaching passage 8, followed by estimation of cell number, cell doubling time (CDT), population doubling (PD) and cell viability. In addition, multilineage differentiation, Colony-Forming Units (CFUs) assay and immunophenotypic analyses were performed. HLA-G expression in MSCs derived from vitrified samples was evaluated by immunohistochemistry, RT-PCR/PCR, mixed lymphocyte reaction (MLR) and immunofluorescence. MSCs derived from non-vitrified WJ tissue were used in order to validate the results obtained from the above methods. Results: MSCs were successfully obtained from vitrified WJ tissues retaining their morphological and multilineage differentiation properties. Furthermore, MSCs from vitrified WJ tissues successfully expressed HLA-G. Conclusion: The above results indicated the successful expression of HLA-G by MSCs from vitrified WJ tissues, thus making them ideal candidates for immunomodulation.
机译:背景:沃顿商学院的果冻(WJ)组织的间质基质细胞(MSC)表达HLA-G,该分子具有多种免疫特性。这项研究旨在评估玻璃化WJ组织来源的MSC中HLA-G的表达。方法:从人的脐带中分离出WJ组织样品,使用VS55溶液进行玻璃化,并在-196°C下保存1年。储存1年后,将WJ组织融化并分离MSC。然后,使MSCs扩增直至到达第8代,然后估计细胞数,细胞倍增时间(CDT),群体倍增(PD)和细胞生存力。此外,进行了多谱系分化,集落形成单位(CFU)测定和免疫表型分析。通过免疫组织化学,RT-PCR / PCR,混合淋巴细胞反应(MLR)和免疫荧光评估了来自玻璃化样品的MSC中HLA-G的表达。为了验证从上述方法获得的结果,使用了非玻璃化WJ组织来源的MSC。结果:成功地从玻璃化的WJ组织中获得了MSC,并保留了它们的形态学和多谱系分化特性。此外,来自玻璃化的WJ组织的MSC成功表达了HLA-G。结论:以上结果表明,MSCs在玻璃化WJ组织中成功表达了HLA-G,因此使其成为免疫调节的理想候选者。

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