In mammals, two tissues are primarily responsible for adaptive thermogenesis: brown fat and beige fat. Although brown fat has long been known as a specialized thermogenic tissue, beige adipocytes, a morphologically distinct type of fat cells that develop within white fat depots upon exposure to cold or high-fat diet, have been discovered only recently. Similar to brown adipocytes, beige adipocytes contain abundant mitochondria and seem to express mitochondrial uncoupling protein 1 (UCP1), which promotes mitochondrial production of heat by increasing the passive proton (H+) leak of the inner mitochondrial membrane. However, the mechanisms of mitochondrial uncoupling and thermogenesis in various beige fat depots as well as the relative contribution of UCP1 remain unclear. Moreover, brown and beige adipocytes retain partial thermogenic capacity even in UCP1-deficient mice. Therefore, this proposal is focused on the identification and characterization of UCP1-dependent and UCP1-independent mechanisms of thermogenesis in brown and beige fat. To this end, we developed a technique for direct patch-clamp recording from vesicles of the whole intact inner mitochondrial membrane (mitoplasts), which for the first time allowed high-resolution functional analysis of mitochondrial ion channels and transporters in their native membrane environment. Using this method, we have succeeded in recording thermogenic UCP1-dependent H+ leak currents across the inner mitochondrial membrane of brown and beige fat. Interestingly, not all beige fat depots possess this UCP1- dependent mitochondrial H+ leak, and using UCP1-deficient mice we also have discovered a novel UCP1- independent mechanism of mitochondrial uncoupling and thermogenesis in both brown and beige adipocytes. This proposal has a single specific aim: to characterize the mechanisms of mitochondrial uncoupling and thermogenesis in adipose tissues. Because adaptive thermogenesis in brown and beige fat consumes large amounts of energy from fat depots and reduces body adiposity and weight, this project will aid the development of therapeutic interventions to control obesity and diabetes.

Public Health Relevance

This project will characterize the molecular mechanisms responsible for heat production in two specialized thermogenic tissues: brown fat and beige fat. The identification of these mechanisms will not only provide an improved understanding of the basic principles of physiological temperature control but also suggest new strategies for pharmacological interventions in obesity and aging.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM107710-02
Application #
9139961
Study Section
Neurotransporters, Receptors, and Calcium Signaling Study Section (NTRC)
Program Officer
Anderson, Vernon
Project Start
2015-09-08
Project End
2019-06-30
Budget Start
2016-07-01
Budget End
2017-06-30
Support Year
2
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Physiology
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94118
Bertholet, Ambre M; Kirichok, Yuriy (2017) UCP1: A transporter for H+and fatty acid anions. Biochimie 134:28-34
Bertholet, Ambre M; Kazak, Lawrence; Chouchani, Edward T et al. (2017) Mitochondrial Patch Clamp of Beige Adipocytes Reveals UCP1-Positive and UCP1-Negative Cells Both Exhibiting Futile Creatine Cycling. Cell Metab 25:811-822.e4
Odegaard, Justin I; Lee, Min-Woo; Sogawa, Yoshitaka et al. (2016) Perinatal Licensing of Thermogenesis by IL-33 and ST2. Cell 166:841-854