Boney C M, Moats-Staats B M, Stiles A D, D'Ercole A J
Department of Pediatrics, University of North Carolina, Chapel Hill 27599-7220.
Endocrinology. 1994 Nov;135(5):1863-8. doi: 10.1210/endo.135.5.7525256.
Insulin-like growth factor-I (IGF-I) stimulates the differentiation of preadipocytes, but the expression of IGF-I and IGF-binding proteins (IGFBPs) during the course of adipogenesis has not been investigated. Using two in vitro models, primary mouse preadipocytes and the 3T3-L1 preadipocyte cell line stimulated to differentiate with IGF-I, we studied IGF and IGFBP expression before and during differentiation. Primary preadipocyte cultures expressed IGF-I, IGFBP-2, and IGFBP-4 messenger RNAs (mRNAs), and conditioned medium (CM) contained IGFBP-3 [approximately 46,000 mol wt (M(r))], IGFBP-4 (24,000 M(r)), and a 30,000 M(r) IGFBP identified by immunoblot as IGFBP-2. During differentiation, an additional approximately 34,000 M(r) form of IGFBP-2 was predominant, but IGFBP-2 mRNA decreased, suggesting that a mechanism other than steady state mRNA levels is regulating protein abundance in CM. Like primary cultures, undifferentiated 3T3-L1 cells expressed IGFBP-4 mRNA, but insignificant levels of IGF-I and IGFBP-2 mRNAs. 3T3-L1 cell CM contained IGFBP-3 and IGFBP-4, and with the addition of IGF-I, a 30,000 M(r) IGFBP was also present. This IGFBP was not recognized by antiserum to IGFBP-1, -2, -4, -5, or -6. During differentiation of 3T3-L1 cells, an approximately 34,000 M(r) form of IGFBP-2 was also present in CM. In summary, primary cultures of mouse preadipocytes and 3T3-L1 cells express similar IGFBPs during IGF-I-stimulated adipogenesis. The presence of a larger isoform of IGFBP-2 in a differentiation-dependent manner and a potentially novel IGFBP in response to IGF-I suggests that these IGFBPs may be important in modulating IGF-I action in adipogenesis.
胰岛素样生长因子-I(IGF-I)可刺激前脂肪细胞的分化,但在脂肪生成过程中IGF-I和胰岛素样生长因子结合蛋白(IGFBPs)的表达尚未得到研究。我们使用两种体外模型,即原代小鼠前脂肪细胞和用IGF-I刺激分化的3T3-L1前脂肪细胞系,研究了分化前及分化过程中IGF和IGFBP的表达。原代前脂肪细胞培养物表达IGF-I、IGFBP-2和IGFBP-4信使核糖核酸(mRNAs),条件培养基(CM)中含有IGFBP-3[约46,000道尔顿分子量(M(r))]、IGFBP-4(24,000 M(r))以及通过免疫印迹鉴定为IGFBP-2的30,000 M(r)的IGFBP。在分化过程中,另外一种约34,000 M(r)形式的IGFBP-2占主导,但IGFBP-2 mRNA减少,这表明除了稳态mRNA水平外,还有其他机制调节CM中蛋白质的丰度。与原代培养物一样,未分化的3T3-L1细胞表达IGFBP-4 mRNA,但IGF-I和IGFBP-2 mRNA水平极低。3T3-L1细胞CM中含有IGFBP-3和IGFBP-4,添加IGF-I后,还出现了一种30,000 M(r)的IGFBP。抗血清对IGFBP-1、-2、-4、-5或-6均不能识别这种IGFBP。在3T3-L1细胞分化过程中,CM中也存在一种约34,000 M(r)形式的IGFBP-2。总之,在IGF-I刺激脂肪生成过程中,小鼠前脂肪细胞和3T3-L1细胞的原代培养物表达相似的IGFBPs。以分化依赖方式存在的较大异构体IGFBP-2以及对IGF-I产生反应的潜在新型IGFBP表明,这些IGFBPs可能在调节脂肪生成中IGF-I的作用方面很重要。