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FKBP51通过Akt-p38信号通路相互调节GRα和PPARγ的激活。

FKBP51 reciprocally regulates GRα and PPARγ activation via the Akt-p38 pathway.

作者信息

Stechschulte Lance A, Hinds Terry D, Ghanem Simona S, Shou Weinian, Najjar Sonia M, Sanchez Edwin R

机构信息

Center for Diabetes and Endocrine Research (L.A.S., T.D.H., S.S.G., S.M.N., E.R.S.), Department of Physiology and Pharmacology, University of Toledo College of Medicine, Toledo, Ohio 43614; and Herman B. Wells Center for Pediatric Research (W.S.), Section of Pediatric Cardiology, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana 46202.

出版信息

Mol Endocrinol. 2014 Aug;28(8):1254-64. doi: 10.1210/me.2014-1023. Epub 2014 Jun 16.

Abstract

FK506-binding protein 51 (FKBP51) is a negative regulator of glucocorticoid receptor-α (GRα), although the mechanism is unknown. We show here that FKBP51 is also a chaperone to peroxisome proliferator-activated receptor-γ (PPARγ), which is essential for activity, and uncover the mechanism underlying this differential regulation. In COS-7 cells, FKBP51 overexpression reduced GRα activity at a glucocorticoid response element-luciferase reporter, while increasing PPARγ activity at a peroxisome proliferator response element reporter. Conversely, FKBP51-deficient (knockout) (51KO) mouse embryonic fibroblasts (MEFs) showed elevated GRα but reduced PPARγ activities compared with those in wild-type MEFs. Phosphorylation is known to exert a similar pattern of reciprocal modulation of GRα and PPARγ. Knockdown of FKBP51 in 3T3-L1 preadipocytes increased phosphorylation of PPARγ at serine 112, a phospho-residue that inhibits activity. In 51KO cells, elevated phosphorylation of GRα at serines 220 and 234, phospho-residues that promote activity, was observed. Because FKBP51 is an essential chaperone to the Akt-specific phosphatase PH domain leucine-rich repeat protein phosphatase, Akt signaling was investigated. Elevated Akt activation and increased activation of p38 kinase, a downstream target of Akt that phosphorylates GRα and PPARγ, were seen in 51KO MEFs, causing activation and inhibition, respectively. Inactivation of p38 with PD169316 reversed the effects of FKBP51 deficiency on GRα and PPARγ activities and reduced PPARγ phosphorylation. Last, loss of FKBP51 caused a shift of PPARγ from cytoplasm to nucleus, as previously shown for GRα. A model is proposed in which FKBP51 loss reciprocally regulates GRα and PPARγ via 2 complementary mechanisms: activation of Akt-p38-mediated phosphorylation and redistribution of the receptors to the nucleus for direct targeting by p38.

摘要

FK506结合蛋白51(FKBP51)是糖皮质激素受体α(GRα)的负调节因子,但其机制尚不清楚。我们在此表明,FKBP51也是过氧化物酶体增殖物激活受体γ(PPARγ)的伴侣蛋白,而PPARγ对活性至关重要,并揭示了这种差异调节的潜在机制。在COS-7细胞中,FKBP51过表达降低了糖皮质激素反应元件荧光素酶报告基因处的GRα活性,同时增加了过氧化物酶体增殖物反应元件报告基因处的PPARγ活性。相反,与野生型小鼠胚胎成纤维细胞(MEF)相比,FKBP51缺陷型(敲除)(51KO)小鼠胚胎成纤维细胞显示出GRα活性升高但PPARγ活性降低。已知磷酸化对GRα和PPARγ发挥类似的相互调节模式。在3T3-L1前脂肪细胞中敲低FKBP51会增加PPARγ丝氨酸-112位点的磷酸化,该磷酸化残基会抑制活性。在51KO细胞中,观察到GRα丝氨酸-220和-234位点的磷酸化升高,这些磷酸化残基会促进活性。由于FKBP51是Akt特异性磷酸酶富含亮氨酸重复序列蛋白磷酸酶的必需伴侣蛋白,因此对Akt信号通路进行了研究。在51KO MEF中观察到Akt激活升高以及p38激酶(Akt的下游靶点,可使GRα和PPARγ磷酸化)的激活增加,分别导致激活和抑制。用PD169316使p38失活可逆转FKBP51缺陷对GRα和PPARγ活性的影响,并减少PPARγ磷酸化。最后,FKBP51的缺失导致PPARγ从细胞质转移到细胞核,这与之前GRα的情况相同。我们提出了一个模型,其中FKBP51的缺失通过两种互补机制对GRα和PPARγ进行相互调节:激活Akt-p38介导的磷酸化以及将受体重新分布到细胞核以便由p38直接靶向。

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