Metabolic signaling and energetic environment in the nucleus is critical for cell division and initiation of tissue regeneration after injury. However energy supply routes to nuclear ATP-dependent processes and metabolic signaling circuits that govern cardiomyocyte cell cycle are unknown. Our studies demonstrate that adenylate kinase (AK)-phosphotransfer (2ADP<->ATP+AMP) plays a major role in metabolic signaling and transmission of high-energy phosphoryls from mitochondria to the nucleus to support nuclear transport. Preliminary studies using genetic and siRNA approaches indicate that the AK isoform network is critical for metabolic reprogram- ming facilitating stem cell cardiac differentiation. W have discovered that during cell cycle cytosolic AK1 trans- locates to the nucleus and associates with mitotic spindles to provide energy for cell division. However, AK1 translocation to the nucleus doesn't occur in mitotically arrested adult cardiomyocytes. Furthermore, we have discovered that deficiency of the AK2 isoform, which is localized in mitochondria, arrests stem cell develop- mental programming and is embryonically lethal. Using 18O-labeling technology we demonstrate that heart re-generative capacity depends on AK2 expression and dynamics of AMP-signaling through AK-AMP-AMPK axis which is a part of p53/p21/cyclin metabolic checkpoint regulating G1/S cell cycle transition. This highlights the significance of AK isoform and AMP-signaling network in regulating nuclear energetics and cell cycle. However molecular mechanisms of AK translocation to the nucleus and association with mitotic spindle and cytokinesis apparatus and the significance of AK and AMP-signaling in energy support of cell cycle, cardiomyocyte renewal and heart regeneration are unknown. Objective/Hypothesis: Based on new discoveries we will test hypothesis that nuclear translocation of AK isoforms and AMP-signaling is critical for the energetics of the cardiomyocyte cell cycle, and that AK-AMP-AMPK signaling axis is a key part of G1/S metabolic checkpoint licensing cardiomyocyte renewal and heart regeneration.
The Specific Aims will determine:
Aim #1 The significance of the AK isoforms in cardiomyocyte nuclear energetics and energy support of cell cycle machinery and AMP-signaling dependent metabolic checkpoint regulating heart regenerative potential.
Aim #2 Molecular mechanisms of cell cycle dependent translocation of AK isoforms to the cell nucleus and association with mitotic spindles and cytokinesis machinery and the role in integration of mitochondrial and nuclear energetic processes.
Aim #3 Mechanisms regulating AK isoform expression, cytosolic-nuclear distribution and AMP signaling by metabolic and growth factors in order to promote nuclear energetics and metabolic checkpoint facilitating stem cell cardiac differentiation and adult cardiomyocyte cell cycle required for heart regeneration. The expected outcome and the novelty of this application will be in defining for the first time molecular mechanisms governing nuclear energetics and AMP-signaling circuits during cell cycle and cell differentiation critical for cardiogenesis, heart renewal and regeneration. Public Health Relevance: Heart regeneration after injury is an emerging critical area in cardiovascular biology and medicine. Successful repair of injured heart requires stimulation of cardiomyocyte regeneration which is one of the most urgent problems in cardiovascular biology and medicine. This innovative study will discover molecular mechanisms and establish rationale and foundation for the development methods for targeted regulation of nuclear energetic and AMP-metabolic signaling circuits to facilitate cardiac differentiation and heart regeneration which would have critical impact for regenerative medicine. Specifically, we will develop approaches for targeting AK isoforms to the nucleus and for regulation of AK expression and AMP-signaling by metabolic and growth factors to promote energetics and re-entry of adult cardiomyocytes into cell cycle.

Public Health Relevance

Heart regeneration after injury is an emerging critical area in cardiovascular biology and medicine. Successful repair of injured heart requires stimulation of cardiomyocyte regeneration which is one of the most urgent problems in cardiovascular biology and medicine. This innovative study will discover molecular mechanisms and establish rationale and foundation for the development methods for targeted regulation of nuclear energetic and AMP-metabolic signaling circuits to facilitate cardiac differentiation and heart regeneration which would have critical impact for regenerative medicine. Specifically, we will develop approaches for targeting AK isoforms to the nucleus and for regulation of AK expression and AMP-signaling by metabolic and growth factors to promote energetics and re-entry of adult cardiomyocytes into cell cycle. PUBLIC HEALTH RELEVANCE: Heart regeneration after injury is an emerging critical area in cardiovascular biology and medicine. This application will define for the first time molecular mechanisms governing energetics and metabolic signaling circuits in cell nucleus during cell division cycle critical in stem cell cardiogenesis, heart renewal and regeneration. This innovative study will discover molecular mechanisms and establish approaches for targeting adenylate kinase(AK) isoforms to the cell nucleus and for regulation of AK expression and AMP-signaling by metabolic and growth factors to promote energetics and re-entry of adult cardiomyocytes into cell cycle. This project is a part of Mayo Clinic Regenerative Medicine program where we apply our developed system bioenergetics approach and advance imaging and stable isotope based phosphometabolomic technologies to determine the significance of phosphotransfer and metabolic signaling circuits and energy transfer pathways to the cell nucleus to activate cardiomyocyte cell cycle and facilitate heart regeneration.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
2R01HL085744-06A1
Application #
8578192
Study Section
Myocardial Ischemia and Metabolism Study Section (MIM)
Program Officer
Adhikari, Bishow B
Project Start
2006-07-01
Project End
2017-06-30
Budget Start
2013-09-01
Budget End
2014-06-30
Support Year
6
Fiscal Year
2013
Total Cost
$378,420
Indirect Cost
$140,420
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
006471700
City
Rochester
State
MN
Country
United States
Zip Code
55905
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