Project Title: The coordination of lipid synthesis and degradation in metabolism and aging ABSTRACT/SUMMARY Lipid imbalances are characteristic of obesity and a feature of many age-related ailments and reproductive pathologies in humans. Yet, the relationship between lipid metabolism, aging and reproduction remains poorly studied. We propose to use the nematode C. elegans to characterize this relationship. In particular, we propose to investigate how the balance between lipid synthesis and breakdown influences an organism's rate of aging and health. In C. elegans, eliminating the germline extends lifespan. Besides fertility loss, germline removal is a major challenge to lipid metabolism because the animal needs to stop fat deposition into eggs and reorganize its lipid profile. Thus, germline-less worms provide a unique platform to understand how lipid balance is established in the cells and tissues of complex multicellular animals that are facing major physiological changes. We have discovered that fat production and degradation appear to be increased simultaneously in response to germline loss in worms. We recently demonstrated that in germline-less adults a conserved transcription factor, NHR-49, upregulate fatty-acid ?-oxidation and desaturation- processes that contribute to lipid breakdown and build-up, respectively. Independently, we have also discovered that these two, and many other processes involved in lipid synthesis and degradation, are elevated in response to germline removal by the conserved transcription factors, DAF-16 and TCER-1. These data have led us to hypothesize that the coordinated enhancement of lipid synthesis and breakdown facilitates the adaptation to germline loss by ensuring lipid homeostasis. We propose to test this hypothesis by using molecular genetics, microscopy and biochemical approaches. The knowledge obtained from these studies is likely to reveal fundamental insights into the relationship of lipid metabolism, reproduction and aging. These studies are of relevance to human health and disease because they address major public health issues such as aging and obesity. The discoveries made through these experiments can lead to the discovery of therapeutic interventions targeting age-related ailments and metabolic diseases.

Public Health Relevance

While cold-shock response (CSR) and adaptation mechanisms are well characterized in unicellular organisms, their metazoan equivalents remain poorly understood. In particular, how poikilothermic animals adapt to acute and long-term cold exposure is not well studied. Studies undertaken as part of our R01 (R01AG051659) have provided us a molecular handle to investigate CSR in C. elegans. We propose to do so through this supplement. Upon successful completion, these studies can reveal fundamental knowledge about the molecular mechanisms by which animals respond to short-term and long-term exposure to extreme cold.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
3R01AG051659-03S1
Application #
9869984
Study Section
Program Officer
Fridell, Yih-Woei
Project Start
2016-08-01
Project End
2020-04-30
Budget Start
2019-04-15
Budget End
2019-04-30
Support Year
3
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Pittsburgh
Department
Pediatrics
Type
Schools of Medicine
DUNS #
004514360
City
Pittsburgh
State
PA
Country
United States
Zip Code
15260