Petkov Stoyan G, Anderson Gary B
Department of Animal Science, University of California, Davis, Davis, California 95616, USA.
Cloning Stem Cells. 2008 Jun;10(2):263-76. doi: 10.1089/clo.2007.0085.
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.
胎牛血清(FBS)是一种常用的培养基补充剂,其成分可变且不明确,这给多能干细胞的培养带来了问题。本研究的目的是确定FBS是否可以被成分明确的培养基补充剂Knockout血清替代物(KSR)所取代,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。在添加FBS和KSR的原代培养物中,总集落面积和平均集落面积没有显著差异(分别为421×10³μm²对395×10³μm²,p = 0.68,n = 11;以及6375μm²对6407μm²,p = 0.885)。与添加KSR和生长因子的培养基相比,添加KSR的培养基中的总集落面积和平均集落面积显著更大(分别为505×10³μm²对396×10³μm²,p = 0.016,n = 12;以及8769μm²对6513μm²,p = 0.003)。与仅含KSR的培养基相比,添加FBS的培养基以及添加KSR和生长因子的培养基中的培养物传代次数显著更多(分别为31.1对21.9,p = 0.004,n = 10;以及35.5对21.6,p = 0.002,n = 10)。在无血清条件下培养的猪EGC对多能干细胞标志物呈阳性,在多达54代时保持稳定的核型,并且能够在体外分化为来自三个原始胚层的细胞。这些结果将有助于改进和规范猪多能干细胞的培养。