Corum Daniel G, Jenkins Dorea P, Heslop James A, Tallent Lacey M, Beeson Gyda C, Barth Jeremy L, Schnellmann Rick G, Muise-Helmericks Robin C
Department of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, South Carolina.
Department of Pathology, Medical University of South Carolina, Charleston, South Carolina.
J Biol Chem. 2020 Dec 25;295(52):18091-18104. doi: 10.1074/jbc.RA120.013716. Epub 2020 Oct 21.
Akt3 regulates mitochondrial content in endothelial cells through the inhibition of PGC-1α nuclear localization and is also required for angiogenesis. However, whether there is a direct link between mitochondrial function and angiogenesis is unknown. Here we show that Akt3 depletion in primary endothelial cells results in decreased uncoupled oxygen consumption, increased fission, decreased membrane potential, and increased expression of the mitochondria-specific protein chaperones, HSP60 and HSP10, suggesting that Akt3 is required for mitochondrial homeostasis. Direct inhibition of mitochondrial homeostasis by the model oxidant paraquat results in decreased angiogenesis, showing a direct link between angiogenesis and mitochondrial function. Next, in exploring functional links to PGC-1α, the master regulator of mitochondrial biogenesis, we searched for compounds that induce this process. We found that, sildenafil, a phosphodiesterase 5 inhibitor, induced mitochondrial biogenesis as measured by increased uncoupled oxygen consumption, mitochondrial DNA content, and voltage-dependent anion channel protein expression. Sildenafil rescued the effects on mitochondria by Akt3 depletion or pharmacological inhibition and promoted angiogenesis, further supporting that mitochondrial homeostasis is required for angiogenesis. Sildenafil also induces the expression of PGC-1 family member PRC and can compensate for PGC-1α activity during mitochondrial stress by an Akt3-independent mechanism. The induction of PRC by sildenafil depends upon cAMP and the transcription factor CREB. Thus, PRC can functionally substitute during Akt3 depletion for absent PGC-1α activity to restore mitochondrial homeostasis and promote angiogenesis. These findings show that mitochondrial homeostasis as controlled by the PGC family of transcriptional activators is required for angiogenic responses.
Akt3通过抑制PGC-1α的核定位来调节内皮细胞中的线粒体含量,并且血管生成也需要Akt3。然而,线粒体功能与血管生成之间是否存在直接联系尚不清楚。在这里,我们表明,原代内皮细胞中Akt3的缺失会导致解偶联氧消耗减少、裂变增加、膜电位降低以及线粒体特异性蛋白伴侣HSP60和HSP10的表达增加,这表明Akt3是线粒体稳态所必需的。模型氧化剂百草枯对线粒体稳态的直接抑制导致血管生成减少,这表明血管生成与线粒体功能之间存在直接联系。接下来,在探索与线粒体生物发生的主要调节因子PGC-1α的功能联系时,我们寻找诱导这一过程的化合物。我们发现,磷酸二酯酶5抑制剂西地那非通过增加解偶联氧消耗、线粒体DNA含量和电压依赖性阴离子通道蛋白表达来诱导线粒体生物发生。西地那非通过Akt3缺失或药理学抑制挽救了对线粒体的影响,并促进了血管生成,进一步支持了血管生成需要线粒体稳态。西地那非还诱导PGC-1家族成员PRC的表达,并可通过一种不依赖Akt3的机制在应激期间补偿PGC-1α的活性。西地那非对PRC的诱导依赖于cAMP和转录因子CREB。因此,在Akt3缺失期间,PRC可以在功能上替代缺失的PGC-1α活性,以恢复线粒体稳态并促进血管生成。这些发现表明,由转录激活因子PGC家族控制的线粒体稳态是血管生成反应所必需的。