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首页> 外文期刊>Stem Cells >Human serum from platelet-poor plasma for the culture of primary human preadipocytes.
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Human serum from platelet-poor plasma for the culture of primary human preadipocytes.

机译:来自贫血小板血浆的人血清,用于培养原代人前脂肪细胞。

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摘要

In adipose tissue engineering, the use of human serum is essential to achieve the goal of an autologous system. Serum from conventional human plasma (SCP) contains platelet-derived growth factor (PDGF), a growth factor known to be both a potent inhibitor of adipose differentiation and also the most important stimulator of proliferation in human serum. Serum from platelet-poor plasma (SPPP) is considered to be PDGF-deprived and should therefore inhibit the differentiation of preadipocytes to adipocytes to a lesser extent. Effective cultivation of preadipocytes with SPPP requires compensating for the missing stimulatory PDGF effect on proliferation. However, the addition of other growth factors to the media needs to provide stimulation of proliferation without significant inhibition of differentiation. Primary human preadipocytes were isolated from adipose tissue samples of 10 healthy human donors and cultured under four different medium conditions (SCP, SPPP, SPPP + 1 nM basic fibroblast growth factor [bFGF], and SPPP + 1 nM epidermal growth factor [EGF]) for five generations. Proliferation activity and differentiation capacity were assessed for each sample, generation, and culture condition by calculating doubling time and measuring glycerol-3-phosphate dehydrogenase (GPDH)-specific activity. The use of SPPP resulted in a marked rise in GPDH activity compared with the cells cultured with SCP. Supplementing SPPP with 1 nM bFGF or EGF increased proliferation activity significantly. SPPP can be considered superior to SCP for the culture of primary human preadipocytes in adipose tissue engineering in terms of proliferation activity and differentiation capacity.
机译:在脂肪组织工程中,使用人血清对于实现自体系统的目标至关重要。常规人血浆(SCP)的血清中含有血小板衍生的生长因子(PDGF),该生长因子既是脂肪分化的有效抑制剂,也是人类血清中最重要的增殖刺激物。贫血小板血浆(SPPP)的血清被认为是PDGF缺乏的,因此应在较小程度上抑制前脂肪细胞向脂肪细胞的分化。用SPPP有效培养前脂肪细胞需要补偿缺失的PDGF对增殖的刺激作用。但是,向培养基中添加其他生长因子需要刺激增殖而又不显着抑制分化。从10个健康人类供体的脂肪组织样本中分离出原代人前脂肪细胞,并在四种不同的培养基条件下培养(SCP,SPPP,SPPP + 1 nM碱性成纤维细胞生长因子[bFGF]和SPPP + 1 nM表皮生长因子[EGF])五代。通过计算倍增时间并测量甘油3-磷酸脱氢酶(GPDH)的比活性,评估每个样品,世代和培养条件的增殖活性和分化能力。与用SCP培养的细胞相比,使用SPPP导致GPDH活性显着提高。用1 nM bFGF或EGF补充SPPP可显着增加增殖活性。就增殖活性和分化能力而言,对于脂肪组织工程中原代人前脂肪细胞的培养,可以认为SPPP优于SCP。

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