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DeltaFosB转录因子的过表达可增加骨形成并抑制脂肪生成。

Overexpression of DeltaFosB transcription factor(s) increases bone formation and inhibits adipogenesis.

作者信息

Sabatakos G, Sims N A, Chen J, Aoki K, Kelz M B, Amling M, Bouali Y, Mukhopadhyay K, Ford K, Nestler E J, Baron R

机构信息

Departments of Cell Biology and Orthopaedics, Yale University School of Medicine SHM IE-55, 333 Cedar St, New Haven, Connecticut 06520-8044, USA.

出版信息

Nat Med. 2000 Sep;6(9):985-90. doi: 10.1038/79683.

Abstract

Members of the AP-1 family of transcription factors participate in the regulation of bone cell proliferation and differentiation. We report here a potent AP-1-related regulator of osteoblast function: DeltaFosB, a naturally occurring truncated form of FosB that arises from alternative splicing of the fosB transcript and is expressed in osteoblasts. Overexpression of DeltaFosB in transgenic mice leads to increased bone formation throughout the skeleton and a continuous post-developmental increase in bone mass, leading to osteosclerosis. In contrast, DeltaFosB inhibits adipogenesis both in vivo and in vitro, and downregulates the expression of early markers of adipocyte differentiation. Because osteoblasts and adipocytes are thought to share a common precursor, it is concluded that DeltaFosB transcriptionally regulates osteoblastogenesis, possibly at the expense of adipogenesis.

摘要

转录因子AP-1家族的成员参与骨细胞增殖和分化的调控。我们在此报告一种强大的与AP-1相关的成骨细胞功能调节因子:DeltaFosB,它是FosB的一种天然截短形式,由fosB转录本的可变剪接产生,并在成骨细胞中表达。在转基因小鼠中过表达DeltaFosB会导致全身骨骼的骨形成增加,以及发育后骨量持续增加,从而导致骨硬化。相反,DeltaFosB在体内和体外均抑制脂肪生成,并下调脂肪细胞分化早期标志物的表达。由于成骨细胞和脂肪细胞被认为有共同的前体,因此得出结论,DeltaFosB通过转录调控成骨细胞生成,可能是以牺牲脂肪生成为代价。

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