Tanaka T, Yoshida N, Kishimoto T, Akira S
Department of Biochemistry, Hyogo College of Medicine, 1-1 Mukogawa-cho, Nishinomiya, Hyogo 663, Japan.
EMBO J. 1997 Dec 15;16(24):7432-43. doi: 10.1093/emboj/16.24.7432.
To investigate the role of C/EBP family members during adipocyte differentiation in vivo, we have generated mice lacking the C/EBPbeta and/or C/EBPdelta by gene targeting. Approximately 85% of C/EBPbeta(-/-).delta(-/-) mice died at the early neonatal stage. By 20 h after birth, brown adipose tissue of the interscapular region in wild-type mice contained many lipid droplets, whereas C/EBPbeta(-/-).delta(-/-) mice did not accumulate droplets. In addition, the epidydimal fat pad weight of surviving adult C/EBPbeta(-/-).delta(-/-) mice was significantly reduced compared with wild-type mice. However, these adipose tissues in C/EBPbeta(-/-).delta(-/-) mice exhibit normal expression of C/EBPalpha and PPARgamma, despite impaired adipogenesis. These results demonstrated that C/EBPbeta and C/EBPdelta have a synergistic role in terminal adipocyte differentiation in vivo. The induction of C/EBPalpha and PPARgamma does not always require C/EBPbeta and C/EBPdelta, but co-expression of C/EBPalpha and PPARgamma is not sufficient for complete adipocyte differentiation in the absence of C/EBPbeta and C/EBPdelta.
为了研究C/EBP家族成员在体内脂肪细胞分化过程中的作用,我们通过基因打靶技术培育出了缺乏C/EBPβ和/或C/EBPδ的小鼠。大约85%的C/EBPβ(-/-).δ(-/-)小鼠在新生儿早期死亡。出生后20小时,野生型小鼠肩胛间区域的棕色脂肪组织含有许多脂滴,而C/EBPβ(-/-).δ(-/-)小鼠没有积累脂滴。此外,存活的成年C/EBPβ(-/-).δ(-/-)小鼠的附睾脂肪垫重量与野生型小鼠相比显著降低。然而,尽管脂肪生成受损,但C/EBPβ(-/-).δ(-/-)小鼠的这些脂肪组织中C/EBPα和PPARγ的表达正常。这些结果表明,C/EBPβ和C/EBPδ在体内终末脂肪细胞分化中具有协同作用。C/EBPα和PPARγ的诱导并不总是需要C/EBPβ和C/EBPδ,但在没有C/EBPβ和C/EBPδ的情况下,C/EBPα和PPARγ的共表达不足以实现完全的脂肪细胞分化。