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TGFB-INHB/activin signaling regulates age-dependent autophagy and cardiac health through inhibition of MTORC2
Kai Chang, Ping Kang, Ying Liu, Kerui Huang, Ting Miao, Antonia P. Sagona, Ioannis P. Nezis, Rolf Bodmer, Karen Ocorr, Hua Bai
Autophagy · 2019 · ▲ 85 citations
Deregulated nutrient-sensing
Mitochondrial dysfunction
Altered intercellular communication
Disabled macroautophagy
Rapamycin / mTOR inhibition
Drosophila
Abstract
Age-related impairment of macroautophagy/autophagy(definition) and loss of cardiac tissue homeostasis contribute significantly to cardiovascular diseases later in life. MTOR(definition) (mechanistic target of rapamycin(definition) 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 Drosophila 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 daw 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 daw knockdown flies. Lastly, either daw knockdown or rictor 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.Abbreviations: AI: arrhythmia index; BafA1: bafilomycin A1; 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
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- 10.1080/15548627.2019.1704117
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APA
Chang, K., Kang, P., Liu, Y., Huang, K., Miao, T., Sagona, A.P., Nezis, I.P., Bodmer, R., Ocorr, K., & Bai, H. (2019). TGFB-INHB/activin signaling regulates age-dependent autophagy and cardiac health through inhibition of MTORC2. <em>Autophagy</em>. https://doi.org/10.1080/15548627.2019.1704117
Vancouver
Chang K, Kang P, Liu Y, Huang K, Miao T, Sagona AP, et al. TGFB-INHB/activin signaling regulates age-dependent autophagy and cardiac health through inhibition of MTORC2. Autophagy. 2019. doi:10.1080/15548627.2019.1704117.
BibTeX
@article{kai2019TGFBIN,
title = {TGFB-INHB/activin signaling regulates age-dependent autophagy and cardiac health through inhibition of MTORC2},
author = {Kai Chang and Ping Kang and Ying Liu and Kerui Huang and Ting Miao and Antonia P. Sagona and Ioannis P. Nezis and Rolf Bodmer and Karen Ocorr and Hua Bai},
journal = {Autophagy},
year = {2019},
doi = {10.1080/15548627.2019.1704117},
}
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