妊娠对大鼠脂肪干细胞增殖的影响。

J. Li, Yayong Zhang, Yimei Wang, J. -. Chen
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引用次数: 3

摘要

干细胞治疗面临许多问题,包括低存活率和低活力。增强干细胞的生物学功能可以提高治疗效果。雌激素水平在怀孕期间升高,影响骨髓间充质干细胞的特性。有证据表明,脂肪源性干细胞(ADSCs)是一种成体间充质干细胞,可用于再生医学。事实上,来自怀孕动物的ADSCs已被用于临床治疗。然而,供体生殖状态对ADSCs增殖的影响尚不清楚。我们研究了17β-雌二醇(E2)和孕酮(P)对实验室大鼠ADSCs体外增殖的影响。取未妊娠组、妊娠组、围产期组、未妊娠组和E2组、未妊娠组和p组5组大鼠,每组15只ADSCs,采用MTT法检测ADSCs的粘附和活力,流式细胞术观察细胞周期。妊娠大鼠ADSCs的增殖率显著高于非妊娠大鼠(P < 0.05);不同妊娠期细胞增殖率差异无统计学意义(P > 0.05)。此外,妊娠大鼠的ADSCs在早期(P1传代)具有更高的粘附性,增殖率也高于非妊娠大鼠的ADSCs。有趣的是,未怀孕大鼠的ADSCs被E2处理,而不是被P处理,其增殖率高于未处理的大鼠。提示ADSCs在不同细胞周期阶段的增殖能力和停留时间可受雌激素浓度等外在因素的调控。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of pregnancy on the proliferation of rat adipose-derived stem cells.
Stem cell therapy faces many problems including poor survival rates and low viability. Enhancing the biological functions of stem cells improves efficacy of therapies. Estrogen, whose levels are elevated during pregnancy, affects the properties of bone marrow mesenchymal stem cells. Evidence suggests that adipose-derived stem cells (ADSCs), which are a type of adult mesenchymal stem cells, can be used in regenerative medicine. In fact, ADSCs from pregnant animals have been used in clinical therapies. However, the effect of the donor's reproductive status on proliferation of ADSCs is unknown. We investigated the effect of 17β-estradiol (E2) and progesterone (P) on the in vitro proliferation of ADSCs from laboratory rats. ADSCs were obtained from five different groups of 15 rats each - non-pregnant, pregnant, in perinatal period, non-pregnant and treated with E2, and non-pregnant and treated with P. Adhesion and viability of ADSCs were determined by MTT assay, and cell cycle was followed by flow cytometry. The proliferation rate of ADSCs from pregnant rats was significantly higher than those from the non-pregnant rats (P < 0.05); however, there was no statistically significant difference in proliferation rates during different phases of pregnancy (P > 0.05). Additionally, ADSCs from pregnant rats possess higher adhesion property in early stage (P1 passage) and higher proliferation rate than ADSCs from non-pregnant rats. Interestingly, ADSCs from non-pregnant rats that were treated with E2, but not those treated with P, showed higher proliferation rates than those from their untreated counterparts. These results suggest that the proliferative capacity and residence time in different cell cycle phases of ADSCs can be regulated by extrinsic factors such as estrogen concentration.
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