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Kinase signaling cascades that modulate peroxisome proliferator-activated receptors

机译:调节过氧化物酶体增殖物激活受体的激酶信号转导级联

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摘要

Peroxisome proliferator-activated receptors (PPARs) are nuclear receptors involved in lipid and glucose homeostasis, inflammation and wound healing. In addition to ligand binding, phosphorylation can also regulate PPARs; the biological effects of phosphorylation depend on the stimulus, the kinase, the PPAR isotype, the residue modified, the cell type and the promoter investigated. The study of this dual regulation mode, which allows PPARs to integrate signals conveyed by lipophilic ligands with those coming from the plasma membrane, may ultimately offer new therapeutic strategies.
机译:过氧化物酶体增殖物激活受体(PPAR)是参与脂质和葡萄糖稳态,炎症和伤口愈合的核受体。除配体结合外,磷酸化还可以调节PPAR。磷酸化的生物学效应取决于所研究的刺激,激酶,PPAR同种型,修饰的残基,细胞类型和启动子。对这种双重调节模式的研究允许PPAR整合亲脂性配体所传递的信号与质膜所传递的信号,最终可能会提供新的治疗策略。

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