Boney C M, Fiedorek F T, Paul S R, Gruppuso P A
Department of Pediatrics, Brown University, Providence, Rhode Island 02903.
Endocrinology. 1996 Jul;137(7):2923-8. doi: 10.1210/endo.137.7.8770915.
Preadipocyte factor-1 (Pref-1), a novel gene product isolated from murine preadipocyte 3T3-L1 cells, is thought to function as a negative regulator of adipocyte differentiation. We investigated the regulation of Pref-1 expression in 3T3-L1 preadipocytes during proliferation, growth arrest, and early differentiation in the presence and absence of three well described differentiation antagonists: interleukin-11 (IL-11), transforming growth factor-beta, and tumor necrosis factor-alpha. Northern blot analysis was used to determine messenger RNA (mRNA) steady state expression of Pref-1 and two differentiation-specific genes, adipsin and glycerol-3-phosphate dehydrogenase. We confirmed that Pref-1 mRNA is abundant in proliferating preadipocytes and that its expression is dramatically reduced early in differentiation. However, proliferating and growth-arrested cells treated with the differentiation inhibitor IL-11 demonstrated a modest decrease in Pref-1 mRNA abundance. Transforming growth factor-beta and tumor necrosis factor-alpha had little effect. The reduction of Pref-1 mRNA was most dramatic in differentiating preadipocytes treated with IL-11, occurring despite inhibition of adipogenesis, as judged by cell morphology and adipocyte-specific gene expression (adipsin and glycerol-3-phosphate dehydrogenase). This effect of IL-11 on Pref-1 suggests that different mechanisms are responsible for the IL-11-induced and the differentiation- associated down-regulation of Pref-1, thus dissociating Pref-1 regulation from differentiation. We conclude that Pref-1 expression is not a reliable marker of preadipocytes, and that decreased Pref-1 abundance does not function as a trigger for adipocyte differentiation.
前脂肪细胞因子-1(Pref-1)是从小鼠前脂肪细胞3T3-L1中分离出的一种新型基因产物,被认为是脂肪细胞分化的负调节因子。我们研究了在有和没有三种已明确描述的分化拮抗剂(白细胞介素-11(IL-11)、转化生长因子-β和肿瘤坏死因子-α)存在的情况下,3T3-L1前脂肪细胞在增殖、生长停滞和早期分化过程中Pref-1表达的调节情况。采用Northern印迹分析来确定Pref-1以及两个分化特异性基因(脂肪酶和甘油-3-磷酸脱氢酶)的信使核糖核酸(mRNA)稳态表达。我们证实Pref-1 mRNA在增殖的前脂肪细胞中含量丰富,并且其表达在分化早期显著降低。然而,用分化抑制剂IL-11处理的增殖和生长停滞细胞中,Pref-1 mRNA丰度有适度下降。转化生长因子-β和肿瘤坏死因子-α的影响很小。在用IL-11处理的分化前脂肪细胞中,Pref-1 mRNA的减少最为显著,尽管根据细胞形态和脂肪细胞特异性基因表达(脂肪酶和甘油-3-磷酸脱氢酶)判断脂肪生成受到抑制,但这种情况仍然发生。IL-11对Pref-1的这种作用表明,IL-11诱导的和与分化相关的Pref-1下调是由不同机制引起的,从而使Pref-1的调节与分化脱钩。我们得出结论,Pref-1表达不是前脂肪细胞的可靠标志物,并且Pref-1丰度的降低并非脂肪细胞分化的触发因素。