Department of Genetics, Development, and Cell Biology, Iowa State University , Ames, IA, USA.
School of Life Sciences, University of Warwick , Coventry, UK.
Autophagy. 2020 Oct;16(10):1807-1822. doi: 10.1080/15548627.2019.1704117. Epub 2019 Dec 29.
Age-related impairment of macroautophagy/autophagy and loss of cardiac tissue homeostasis contribute significantly to cardiovascular diseases later in life. MTOR (mechanistic target of rapamycin kinase) signaling is the most well-known regulator of autophagy, cellular homeostasis, and longevity. The MTOR signaling consists of two structurally and functionally distinct multiprotein complexes, MTORC1 and MTORC2. While MTORC1 is well characterized but the role of MTORC2 in aging and autophagy remains poorly understood. Here we identified TGFB-INHB/activin signaling as a novel upstream regulator of MTORC2 to control autophagy and cardiac health during aging. Using heart as a model system, we show that cardiac-specific knockdown of TGFB-INHB/activin-like protein daw induces autophagy and alleviates age-related heart dysfunction, including cardiac arrhythmias and bradycardia. Interestingly, the downregulation of activates TORC2 signaling to regulate cardiac autophagy. Activation of TORC2 alone through overexpressing its subunit protein rictor promotes autophagic flux and preserves cardiac function with aging. In contrast, activation of TORC1 does not block autophagy induction in knockdown flies. Lastly, either knockdown or overexpression in fly hearts prolongs lifespan, suggesting that manipulation of these pathways in the heart has systemic effects on longevity control. Thus, our studies discover the TGFB-INHB/activin-mediated inhibition of TORC2 as a novel mechanism for age-dependent decreases in autophagic activity and cardiac health. AI: arrhythmia index; BafA1: bafilomycin A; BMP: bone morphogenetic protein; CQ: chloroquine; CVD: cardiovascular diseases; DI: diastolic interval; ER: endoplasmic reticulum; HP: heart period; HR: heart rate; MTOR: mechanistic target of rapamycin kinase; NGS: normal goat serum; PBST: PBS with 0.1% Triton X-100; PDPK1: 3-phosphoinositide dependent protein kinase 1; RICTOR: RPTOR independent companion of MTOR complex 2; ROI: region of interest; ROUT: robust regression and outlier removal; ROS: reactive oxygen species; R-SMAD: receptor-activated SMAD; SI: systolic interval; SOHA: semi-automatic optical heartbeat analysis; TGFB: transformation growth factor beta; TSC1: TSC complex subunit 1.
年龄相关的巨自噬/自噬损伤和心脏组织内稳态的丧失,显著促进了生命后期心血管疾病的发生。雷帕霉素靶蛋白(mTOR)信号是自噬、细胞内稳态和长寿的最著名调节因子。mTOR 信号由两个结构和功能上不同的多蛋白复合物组成,mTORC1 和 mTORC2。尽管 mTORC1 已得到很好的描述,但 mTORC2 在衰老和自噬中的作用仍知之甚少。在这里,我们发现 TGFB-INHB/激活素信号是控制衰老过程中 mTORC2 自噬和心脏健康的新的上游调节剂。我们以心脏为模型系统,表明心脏特异性敲低 TGFB-INHB/激活素样蛋白 daw 可诱导自噬并减轻与年龄相关的心脏功能障碍,包括心律失常和心动过缓。有趣的是,下调 可激活 TORC2 信号来调节心脏自噬。通过过表达其亚基蛋白 rictor 单独激活 TORC2 会促进自噬通量并随着年龄的增长维持心脏功能。相比之下,在 daw 敲低的果蝇中,激活 TORC1 并不能阻止自噬的诱导。最后,果蝇心脏中 daw 的敲低或过表达均可延长寿命,表明心脏中这些途径的操作对长寿控制具有系统影响。因此,我们的研究发现 TGFB-INHB/激活素介导的 TORC2 抑制是与年龄相关的自噬活性和心脏健康下降的新机制。AI:心律失常指数;BafA1:巴弗霉素 A;BMP:骨形态发生蛋白;CQ:氯喹;CVD:心血管疾病;DI:舒张间隔;ER:内质网;HP:心动周期;HR:心率;MTOR:雷帕霉素靶蛋白激酶;NGS:正常山羊血清;PBST:含 0.1%Triton X-100 的 PBS;PDPK1:3-磷酸肌醇依赖的蛋白激酶 1;RICTOR:mTORC2 复合物的 RPTOR 独立伴侣;ROI:感兴趣区域;ROUT:稳健回归和异常值剔除;ROS:活性氧;R-SMAD:受体激活的 SMAD;SI:收缩间隔;SOHA:半自动光学心跳分析;TGFB:转化生长因子β;TSC1:TSC 复合物亚基 1。