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Mitochondrial Fission and Liver Function

  • Yisang Yoon(PI)
    ,
  • Yisang Yoon(CoPI)
Grant:
Research project
Project status
Finished

About the Project

DESCRIPTION (provided by applicant): Mitochondrial dysfunction is a major cause of liver pathology by participating in oxidative stress and cell death. Mitochondria continually change their morphology and location inside the cell. Dynamic changes in mitochondrial morphology involve mainly fission and fusion of mitochondrial tubules. However, the functional significance of the dynamic behavior of mitochondria is not well understood. The mitochondrial electron transport chain (ETC) is the major source of reactive oxygen species (ROS) that contributes to oxidative stress conditions. Our studies have demonstrated that inhibiting mitochondrial fission decreases cellular ROS levels in ROS-overproducing conditions, which in turn reduces oxidative stress-induced cell death. Our long-term objectives are to elucidate molecular mechanisms of mitochondrial fission/fusion, and to define the physiological roles of mitochondrial dynamics. In this application, we will continue to study the molecular mechanisms of how mitochondrial fission and fusion proteins control mitochondrial morphology, and investigate the role of mitochondrial dynamics in mitochondrial activity and liver function. The central hypothesis of this proposal is that networks of molecular interactions involving fission and fusion proteins on the mitochondrial membrane regulate mitochondrial morphology and function, and play an integral role in health and pathology of the liver. In the first specific aim, we will study the molecular mechanisms that control the fission/fusion balance of mitochondria. In the second specific aim, we will investigate the involvement of the mitochondrial fission protein hFis1 in mitochondrial fission and apoptosis. The third specific aim is to understand the physiological significance of mitochondrial morphology by focusing on its relationship with the ETC activity and ROS generation in hepatocytes. We will also test whether mitochondrial fission can be a useful target to control liver injury using a cholestatic liver model how mitochondrial dynamics contribute to the regulation of mitochondrial function and cell physiology in health and diseases of the liver.

Project Information

Project Type

Research project

Project Managed By

Time Period

09/01/2003 – 01/31/2015

Status

Finished

Funding Details

Mitochondrial Fission and Liver FunctionAward
FunderAmount
National Institute of Diabetes and Digestive and Kidney Diseases
237882 USD
Mitochondrial Fission and Liver FunctionAward
FunderAmount
National Institute of Diabetes and Digestive and Kidney Diseases
166024 USD
Regulation of Mitochondrial Morphology in Liver CellsAward
FunderAmount
National Institute of Diabetes and Digestive and Kidney Diseases
230795 USD
Regulation of Mitochondrial Morphology in Liver CellsAward
FunderAmount
National Institute of Diabetes and Digestive and Kidney Diseases
236349 USD
Regulation of Mitochondrial Morphology in Liver CellsAward
FunderAmount
National Institute of Diabetes and Digestive and Kidney Diseases
267356 USD
Regulation of Mitochondrial Morphology in Liver CellsAward
FunderAmount
National Institute of Diabetes and Digestive and Kidney Diseases
224101 USD
Regulation of Mitochondrial Morphology in Liver CellsAward
FunderAmount
National Institute of Diabetes and Digestive and Kidney Diseases
236349 USD
Mitochondrial Fission and Liver FunctionAward
FunderAmount
National Institute of Diabetes and Digestive and Kidney Diseases
303790 USD
Mitochondrial Fission and Liver FunctionAward
FunderAmount
National Institute of Diabetes and Digestive and Kidney Diseases
82758 USD
Mitochondrial Fission and Liver FunctionAward
FunderAmount
National Institute of Diabetes and Digestive and Kidney Diseases
252673 USD