猪胚胎生殖细胞在血清补充和无血清条件下的培养:血清和生长因子对原代和长期培养的影响。

Stoyan G Petkov, Gary B Anderson
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引用次数: 30

摘要

胎牛血清(FBS)是一种常用的培养基补充物,其成分多变且不确定,这在多能干细胞的培养中存在问题。本研究的目的是确定FBS是否可以用敲除血清替代(KSR)替代,这是一种确定的培养基补充物,并研究FBS和生长因子对猪胚胎生殖细胞(EGC)短期和长期培养的影响。在原代培养中,FBS和ksr培养基的总菌落面积和平均菌落面积没有显著差异(421 × 10(3) mum(2) vs. 395 × 10(3) microm(2), p = 0.68, n = 11; 6375 microm(2) vs. 6407 microm(2), p = 0.885)。与添加KSR和生长因子的培养基相比,添加KSR的培养基的总菌落面积和平均菌落面积显著大于添加KSR和生长因子的培养基(505 × 10(3) microm(2) vs. 396 × 10(3) microm(2), p = 0.016, n = 12, 8769 microm(2) vs. 6513 microm(2), p = 0.003)。与仅含KSR的培养基相比,在添加fbs的培养基和添加KSR和生长因子的培养基中培养的传代数显著增加(分别为31.1 vs. 21.9, p = 0.004, n = 10, 35.5 vs. 21.6, p = 002, n = 10)。在无血清条件下维持的猪EGC多能干细胞标记阳性,在54代传代中保持稳定的核型,并且能够在体外从三个主要生殖层分化成细胞。这些结果将有助于改进和规范猪多能干细胞的培养。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Culture of porcine embryonic germ cells in serum-supplemented and serum-free conditions: the effects of serum and growth factors on primary and long-term culture.

Fetal bovine serum (FBS) is a commonly used medium supplement with variable and undefined composition, which presents problems in culture of pluripotent stem cells. The purpose of this study was to determine if FBS can be replaced with Knockout Serum Replacement (KSR), a defined medium supplement, and to examine the effects of FBS and growth factors on short- and long-term culture of pig embryonic germ cells (EGC). No significant differences were observed in total and mean colony areas in primary cultures between FBS- and KSR-supplemented medium (421 x 10(3) mum(2) vs. 395 x 10(3) microm(2), p = 0.68, n = 11, and 6375 microm(2) vs. 6407 microm(2), p = 0.885, respectively). Total and mean colony areas were significantly larger in KSR-supplemented medium compared with medium supplemented with KSR and growth factors (505 x 10(3) microm(2) vs. 396 x 10(3) microm(2), p = 0.016, n = 12, and 8769 microm(2) vs. 6513 microm(2), p = 0.003, respectively). The cultures proliferated for significantly higher numbers of passages in FBS-supplemented medium and in medium supplemented with KSR and growth factors compared with medium containing KSR alone (31.1 vs. 21.9, p = 0.004, n = 10, and 35.5 vs. 21.6, p = 002, n = 10, respectively). Porcine EGC maintained in serum-free conditions were positive for pluripotent stem cell markers, maintained stable karyotypes for up to 54 passages, and were capable of differentiating in vitro into cells from the three primary germ layers. These results will help improve and standardize culture of pluripotent stem cells in the pig.

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