נק' מוניטין:
58,701
Cell. 2015 Feb 26;160(5):842-55. doi: 10.1016/j.cell.2015.02.004.
Neuronal CRTC-1 Governs Systemic Mitochondrial Metabolism and Lifespan via a Catecholamine Signal
Kristopher Burkewitz1, Ianessa Morantte1, Heather J.M. Weir1, Robin Yeo1, Yue Zhang1, Frank K. Huynh2, Olga R. Ilkayeva2, Matthew D. Hirschey2, Ana R. Grant3, William B. Mair1, ,
Highlights
• CRTC-1 uncouples AMPK-mediated longevity from pleiotropic side effects
• AMPK promotes longevity via CRTC-1-dependent remodeling of mitochondrial metabolism
• Neuronal CRTC-1/CREB and NHR-49 antagonistically regulate longevity and metabolism
• Neuronal CRTC-1 regulates mitochondrial dynamics and lifespan via octopamine
Summary
Low energy states delay aging in multiple species, yet mechanisms coordinating energetics and longevity across tissues remain poorly defined. The conserved energy sensor AMP-activated protein kinase (AMPK) and its corresponding phosphatase calcineurin modulate longevity via the CREB regulated transcriptional coactivator (CRTC)-1 in C. elegans. We show that CRTC-1 specifically uncouples AMPK/calcineurin-mediated effects on lifespan from pleiotropic side effects by reprogramming mitochondrial and metabolic function. This pro-longevity metabolic state is regulated cell nonautonomously by CRTC-1 in the nervous system. Neuronal CRTC-1/CREB regulates peripheral metabolism antagonistically with the functional PPARα ortholog, NHR-49, drives mitochondrial fragmentation in distal tissues, and suppresses the effects of AMPK on systemic mitochondrial metabolism and longevity via a cell-nonautonomous catecholamine signal. These results demonstrate that while both local and distal mechanisms combine to modulate aging, distal regulation overrides local contribution. Targeting central perception of energetic state is therefore a potential strategy to promote healthy aging.
