Department of Cancer Biology and Genetics, College of Medicine, The Ohio State University, Columbus, OH 43210, USA; The Ohio State University Comprehensive Cancer Center, Columbus, OH 43210, USA.
Department of Cancer Biology and Genetics, College of Medicine, The Ohio State University, Columbus, OH 43210, USA; The Ohio State University Comprehensive Cancer Center, Columbus, OH 43210, USA.
Mol Metab. 2019 Dec;30:48-60. doi: 10.1016/j.molmet.2019.09.008. Epub 2019 Sep 28.
Despite the large body of work describing the tumor suppressor functions of Phosphatase and tensin homologue deleted on chromosome ten (PTEN), its roles in adipose homeostasis of adult animals are not yet fully understood. Here, we sought to determine the role of PTEN in whole-body adipose homeostasis.
We genetically manipulated PTEN in specific fat depots through recombinant adeno-associated viral vector (rAAV)-based gene transfer of Cre recombinase to adult PTEN mice. Additionally, we used a denervation agent, 6OHDA, to assess the role of sympathetic signaling in PTEN-related adipose remodeling. Furthermore, we chemically manipulated AKT signaling via a pan-AKT inhibitor, MK-2206, to assess the role of AKT in PTEN-related adipose remodeling. Finally, to understand the role of leptin and central signaling on peripheral tissues, we knocked down hypothalamic leptin receptor with a microRNA delivered by a rAAV vector.
Knockdown PTEN in individual fat depot resulted in massive expansion of the affected fat depot through activation of AKT signaling associated with suppression of lipolysis and induction of leptin. This hypertrophic expansion of the affected fat depot led to upregulation of PTEN level, higher lipolysis, and induction of white fat browning in other fat depots, and the compensatory reduced fat mass to maintain a set point of whole-body adiposity. Administration of AKT inhibitor MK-2206 prevented the adipose PTEN knockdown-associated effects. 6OHDA-mediated denervation demonstrated that sympathetic innervation was required for the PTEN knockdown-induced adipose redistribution. Knockdown hypothalamic leptin receptor attenuated the adipose redistribution induced by PTEN deficiency in individual fat depot.
Our results demonstrate the essential role of PTEN in adipose homeostasis, including mass and distribution in adulthood, and reveal an "adipose PTEN-leptin-sympathetic nervous system" feedback loop to maintain a set point of adipose PTEN and whole-body adiposity.
尽管有大量研究描述了磷酸酶和张力蛋白同源物缺失的肿瘤抑制因子(PTEN)的肿瘤抑制功能,但它在成年动物脂肪稳态中的作用尚不完全清楚。在这里,我们试图确定 PTEN 在全身脂肪稳态中的作用。
我们通过重组腺相关病毒(rAAV)载体介导的 Cre 重组酶基因转移,在特定的脂肪组织中遗传操纵 PTEN。此外,我们使用去神经剂 6-羟基多巴胺(6OHDA)来评估交感神经信号在 PTEN 相关脂肪重塑中的作用。此外,我们通过泛 AKT 抑制剂 MK-2206 化学操纵 AKT 信号,以评估 AKT 在 PTEN 相关脂肪重塑中的作用。最后,为了了解瘦素和中枢信号对周围组织的作用,我们使用 rAAV 载体递送的 microRNA 敲低下丘脑瘦素受体。
在单个脂肪组织中敲低 PTEN 会通过激活 AKT 信号导致受影响的脂肪组织大量扩张,同时抑制脂肪分解并诱导瘦素产生。受影响的脂肪组织的这种肥大性扩张导致 PTEN 水平上调、脂肪分解增加和其他脂肪组织中白色脂肪棕色化诱导,以及全身脂肪量的补偿性减少,以维持全身脂肪的设定点。AKT 抑制剂 MK-2206 的给药可预防 AKT 抑制剂 MK-2206 预防脂肪组织 PTEN 敲低相关作用。6OHDA 介导的去神经支配表明,交感神经支配是 PTEN 敲低诱导的脂肪再分布所必需的。敲低下丘脑瘦素受体可减弱单个脂肪组织中 PTEN 缺陷引起的脂肪再分布。
我们的研究结果表明,PTEN 在脂肪稳态中起着至关重要的作用,包括成年时的质量和分布,并揭示了一个“脂肪组织 PTEN-瘦素-交感神经系统”反馈回路,以维持脂肪组织 PTEN 和全身脂肪的设定点。