首页> 美国卫生研究院文献>International Journal of Molecular and Cellular Medicine >Proliferation Characterization and Differentiation Potency of Adipose Tissue-Derived Mesenchymal Stem Cells (AT-MSCs) Cultured in Fresh Frozen and non-Fresh Frozen Plasma
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Proliferation Characterization and Differentiation Potency of Adipose Tissue-Derived Mesenchymal Stem Cells (AT-MSCs) Cultured in Fresh Frozen and non-Fresh Frozen Plasma

机译:新鲜和非新鲜冷冻血浆中培养的脂肪组织间充质干细胞(AT-MSC)的增殖鉴定和分化潜能

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摘要

Mesenchymal stem cells (MSCs) have unique properties, including high proliferation rates, self-renewal, and multilineage differentiation ability. Their characteristics are affected by increasing age and microenvironment. This research is aimed to determine the proliferation, characteristics and differentiation capacity of adipose tissue-derived (AT)-MSCs at many passages with different media. The cell proliferation capacity was assayed using trypan blue. MSCs characterization (CD90, CD44, CD105, CD73, CD11b, CD19, CD34, CD45, and HLA-DR) was performed by flow cytometry, and cell differentiation was determined by specific stainings. Population doubling time (PDT) of AT-MSCs treated with fresh frozen plasma (FFP) and non-FFP increased in the late passage (P) (P15 FFP was 22.67 ± 7.01 days and non-FFP was 19.65 ± 2.27 days). Cumulative cell number was significantly different between FFP and non-FFP at P5, 10, 15. AT-MSCs at P4-15 were positive for CD90, CD44, CD105, and CD73, and negative for CD11b, CD19, CD34, CD45, and HLA-DR surface markers. AT-MSCs at P5, 10, 15 had potential toward adipogenic, chondrogenic, and osteogenic differentiation. Therefore, PDT was affected by increased age but no difference was observed in morphology, surface markers and differentiation capacity among passages. Cumulative cell number in FFP was higher in comparison with non-FFP in P5, 10, 15. Our data suggest that FFP may replace FBS for culturing MSCs.
机译:间充质干细胞(MSC)具有独特的特性,包括高增殖率,自我更新和多系分化能力。它们的特征受年龄和微环境的影响。这项研究旨在确定脂肪组织衍生(AT)-MSC在不同培养基中多次传代的增殖,特征和分化能力。使用锥虫蓝测定细胞增殖能力。通过流式细胞术进行MSCs表征(CD90,CD44,CD105,CD73,CD11b,CD19,CD34,CD45和HLA-DR),并通过特异性染色确定细胞分化。用新鲜冷冻血浆(FFP)和非FFP处理的AT-MSC的群体倍增时间(PDT)在后期传代(P)中有所增加(P15 FFP为22.67±7.01天,非FFP为19.65±2.27天)。 FFP和non-FFP在P5、10、15时的累积细胞数量显着不同。P4-15处的AT-MSC对CD90,CD44,CD105和CD73呈阳性,而对CD11b,CD19,CD34,CD45和CD75b呈阴性。 HLA-DR表面标记。在P5、10、15的AT-MSC具有成脂,成软骨和成骨分化的潜力。因此,PDT受年龄增长的影响,但在各代之间的形态,表面标记和分化能力方面没有观察到差异。与P5、10、15中的非FFP相比,FFP中的累积细胞数更高。我们的数据表明,FFP可能取代FBS用于培养MSC。

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