Laboratory of Molecular and Cellular Cardiology, Department of Clinical Biochemistry and Pharmacology, Odense University Hospital, Denmark.
Acta Histochem. 2013 May;115(4):401-6. doi: 10.1016/j.acthis.2012.08.005. Epub 2012 Sep 10.
Downregulation of the preadipocyte marker Delta-like 1 homologue (Dlk1), an inhibitor of adipogenesis, has been suggested to be a prerequisite for adipogenic differentiation to occur, and low Dlk1 levels are often used to verify adipogenesis. Mouse preadipocytic cell lines such as 3T3-L1, as well as primary derived preadipocytes, are important models to study adipogenic differentiation and obesity. However, in vitro adipogenic differentiation of primary derived preadipocytes remains incomplete, and identification of factors that will improve the adipogenic differentiation process is thus of high value. In this study we show that horse serum fails to improve adipogenic differentiation of mouse preadipocytes (both 3T3-L1 cells and primary derived mouse preadipocytes) as otherwise reported for bone marrow derived adipogenic precursors. Unexpectedly, while Dlk1 levels were indeed decreased using horse serum, this did not correlate with a high degree of adipogenic differentiation. In conclusion, our novel results thus reveal that horse serum clearly is insufficient for adipogenic differentiation of mouse preadipocytes and that low levels of Dlk1 alone are a poor marker of mouse in vitro adipogenesis. We would also like to emphasize that it is very important for the field of cellular differentiation that researchers thoroughly investigate the effect of individual reagents in their protocols. Such data will increase understanding of the limitations and possibilities of individual systems.
脂肪细胞前体细胞标志物 Delta-like 1 同源物(Dlk1)的下调被认为是脂肪生成分化发生的前提,低 Dlk1 水平通常用于验证脂肪生成。3T3-L1 等小鼠前体脂肪细胞系以及原代前体脂肪细胞是研究脂肪生成分化和肥胖的重要模型。然而,原代前体脂肪细胞的体外脂肪生成分化仍然不完全,因此确定能够改善脂肪生成分化过程的因素具有重要价值。在这项研究中,我们表明,马血清未能如先前报道的骨髓来源的脂肪生成前体那样改善小鼠前体脂肪细胞(包括 3T3-L1 细胞和原代小鼠前体脂肪细胞)的脂肪生成分化。出乎意料的是,虽然使用马血清确实降低了 Dlk1 水平,但这与高度的脂肪生成分化无关。总之,我们的新结果表明,马血清显然不足以促进小鼠前体脂肪细胞的脂肪生成分化,而 Dlk1 水平低本身就是小鼠体外脂肪生成的一个很差的标志物。我们还想强调,对于细胞分化领域来说,研究人员在其方案中彻底研究单个试剂的影响非常重要。这些数据将增加对各个系统的局限性和可能性的理解。