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Early B-Cell Factor (O/E-1) Is a Promoter of Adipogenesis and Involved in Control of Genes Important for Terminal Adipocyte Differentiation

机译:早期B细胞因子(O / E-1)是脂肪形成的促进剂并参与对终末脂肪细胞分化重要基因的控制

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摘要

Olf-1/early B-cell factor (O/E-1) is a transcription factor important for B-lymphocyte and neuronal gene regulation. Here we report that all three known O/E genes (O/E-1, -2, and -3) are expressed in mouse adipose tissue and are upregulated during adipocyte differentiation. Forced expression of O/E-1 in either the preadipocyte cell line 3T3-L1 or mouse embryonic fibroblasts augmented adipogenesis, and constitutive expression of O/E-1 in uncommitted NIH 3T3 fibroblasts led to initiation of adipocyte differentiation. Furthermore, a dominant negative form of O/E-1 partially suppressed 3T3-L1 adipogenesis, indicating that expression from endogenous O/E target genes is required for 3T3-L1 terminal differentiation. Thus, our data point to the importance of O/E target genes for adipocyte differentiation and suggest a novel role for O/E-1 as an initiator and stimulator of adipogenesis.
机译:Olf-1 /早期B细胞因子(O / E-1)是对B淋巴细胞和神经元基因调控重要的转录因子。在这里我们报告所有三个已知的O / E基因(O / E-1,-2和-3)在小鼠脂肪组织中表达,并在脂肪细胞分化过程中被上调。 O / E-1在脂肪前细胞细胞系3T3-​​L1或小鼠胚胎成纤维细胞中的强迫表达增强了脂肪生成,而O / E-1在未定型的NIH 3T3成纤维细胞中的组成性表达导致脂肪细胞分化的开始。此外,O / E-1的显性负性形式部分抑制了3T3-L1的脂肪形成,表明3T3-L1末端分化需要来自内源性O / E靶基因的表达。因此,我们的数据指出O / E靶基因对于脂肪细胞分化的重要性,并暗示O / E-1作为脂肪形成的引发剂和刺激剂的新作用。

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