Zheng Xiaoyang, Baker Haven, Hancock William S, Fawaz Farah, McCaman Michael, Pungor Erno
Barnett Institute and Department of Chemistry and Chemical Biology, Northeastern University, 341 Mugar Hall, 360 Huntington Avenue, Boston, Massachusetts 02115, USA.
Biotechnol Prog. 2006 Sep-Oct;22(5):1294-300. doi: 10.1021/bp060121o.
Fetal bovine serum (FBS) is the most widely used growth supplement for cell cultures, primarily because of its high levels of growth stimulatory factors and low levels of growth inhibitory factors. Maintaining successful and consistent cell fermentations can be difficult, as FBS is a complex natural product and may vary from lot to lot even from a single manufacturer. The quality and concentration of both bulk and specific proteins can affect cell growth. Quality control tools for FBS are relatively primitive and expensive given the complexity of the sample and the large amounts of FBS used. We undertook this study to examine whether proteomics could be used as a tool to analyze the variability of different fermentation processes. We hypothesized that inconsistent cell growth in fermentations could be due to the quality of FBS and that different lots of FBS had varying concentrations of proteins such as growth stimulatory factors, growth inhibitory factors, and/or other proteins that may correlate with cellular growth rate. To investigate whether this was the case, we grew three batches of adult retinal pigment epithelial cells (ARPE-19) using three different lots of fetal bovine serum (FBS-Ia, FBS-Ib, and FBS-II). We found that the growth rate of the culture was significantly and consistently higher in the FBS-II lot. To determine why the other lots promoted different growth properties, we used proteomic techniques to analyze the protein composition of the three lots. We then performed a time course study to monitor specific changes in individual proteins in the fermentation medium. The amount of several extracellular matrix and structural proteins, which are indicators of cell growth, increased over time. Alternatively, components supplied by the FBS addition, such as nutritional-related and cell-spreading-related proteins, decreased over time.
胎牛血清(FBS)是细胞培养中使用最广泛的生长补充剂,主要是因为其高水平的生长刺激因子和低水平的生长抑制因子。维持成功且一致的细胞发酵可能很困难,因为FBS是一种复杂的天然产物,即使来自单一制造商,不同批次之间也可能存在差异。总体蛋白质和特定蛋白质的质量及浓度都会影响细胞生长。鉴于样品的复杂性和FBS的大量使用,FBS的质量控制工具相对原始且昂贵。我们开展这项研究以检验蛋白质组学是否可作为分析不同发酵过程变异性的工具。我们假设发酵中细胞生长不一致可能归因于FBS的质量,并且不同批次的FBS具有不同浓度的蛋白质,如生长刺激因子、生长抑制因子和/或其他可能与细胞生长速率相关的蛋白质。为了研究是否如此,我们使用三批不同的胎牛血清(FBS - Ia、FBS - Ib和FBS - II)培养了三批成人视网膜色素上皮细胞(ARPE - 19)。我们发现,在FBS - II批次中,培养物的生长速率显著且持续更高。为了确定其他批次为何促进不同的生长特性,我们使用蛋白质组学技术分析了这三个批次的蛋白质组成。然后我们进行了一项时间进程研究,以监测发酵培养基中单个蛋白质的特定变化。几种作为细胞生长指标的细胞外基质和结构蛋白的量随时间增加。另外,添加FBS所提供的成分,如营养相关和细胞铺展相关的蛋白质,随时间减少。