Pyruvate kinase M2 (PKM2) is primarily a tetrameric enzyme that catalyzes the transfer of a phosphate from phosphoenolpyruvate to ADP, resulting in pyruvate and ATP. PKM2 is abundant during embryogenesis and in specific adult tissues such as adipose and pancreatic islets. New evidence suggests that PKM2 expression in these tissues may have a pivotal role in regulating glycolysis, cell death, and proliferation. However, the metabolic functions of PKM2 in these tissues remain largely unexplored. Our preliminary data shows that PKM2 deficiency improved differentiation of 3T3-L1 pre-adipocytes into mature adipocytes and enhanced mitochondrial respiratory capacity. Moreover, PKM2 deficiency in white adipocytes activated a brown fat-like gene program, which translated into increased mitochondria biogenesis and expression of UCP1, BMP7, and PRDM16. To further delineate PKM2 metabolic functions we will employ complementary approaches. First, we will use a cell platform to investigate the metabolic functions of adipose PKM2 ex-vivo and dissect the underlying mechanisms. Then, we will determine the metabolic role of adipose PKM2 in vivo using two approaches: (1) a genetic approach using mice with adipose-specific deletion by crossing adipose-specific Cre mice to PKM2fl/fl mice and (2) a pharmacological approach using currently available specific inhibitors for PKM2. It is envisioned that the successful completion of these studies will lead to a better understanding of the metabolic functions of PKM2 and may provide insights into therapeutic interventions for obesity and diabetes.

Public Health Relevance

The goal of this proposal is to investigate the metabolic functions of adipose pyruvate kinase M2. Pyruvate kinase, a rate- limiting enzyme during glycolysis, catalyzes the generation of pyruvate and ATP from phosphoenolpyruvate and ADP. My preliminary data shows that depletion of PKM2 in white pre-adipocytes promotes the development of a brown fat-like thermogenic program with an increase in UCP1 gene expression. The present proposal identifies PKM2 as a novel component of the molecular circuit that contributes to adipocyte plasticity and adaptive thermogenesis, which may have potential therapeutic implication.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Career Transition Award (K99)
Project #
1K99DK100736-01
Application #
8618816
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Program Officer
Haft, Carol R
Project Start
2013-09-13
Project End
2015-09-12
Budget Start
2013-09-13
Budget End
2014-09-12
Support Year
1
Fiscal Year
2013
Total Cost
$90,000
Indirect Cost
$6,667
Name
University of California Davis
Department
Nutrition
Type
Schools of Earth Sciences/Natur
DUNS #
047120084
City
Davis
State
CA
Country
United States
Zip Code
95618
Bettaieb, Ahmed; Vazquez Prieto, Marcela A; Rodriguez Lanzi, Cecilia et al. (2014) (-)-Epicatechin mitigates high-fructose-associated insulin resistance by modulating redox signaling and endoplasmic reticulum stress. Free Radic Biol Med 72:247-56