Grant: Discovery Grants Program - Individual

Heme is an essential component for oxygen dependent life. I am fascinated by the diverse needs for heme for different cellular mechanisms. My research program is focused on understanding how heme-associated mechanisms are coordinated. Cells either make heme or extract it from the environment. Heme is a substrate, ligand, and essential iron store. Heme is essential to cellular respiration and the formation of cytochromes, globins and nuclear hormone receptors. Heme-proteins are important for many cell functions including metabolism, and communication inside and between cells (from hormones to gases). Heme is an important molecule. Yet, we still do not fully grasp how heme synthesis, storage, degradation or transport is balanced with the biological demands of cells, especially the unique demands in muscle cells (myocytes). The purpose of my research is to understand how heme metabolism is coordinated with the complex biological needs of myocytes. The synthesis of heme is dependent on the mitochondria-that vary in size, shape, content and turnover in different cells and organisms. In myocytes, balancing mitochondrial respiration (for energy) with calcium regulation (for contraction) is very complex and essential for sustaining life. Calcium release inside cells causes myocyte contraction. Energy is consumed for calcium-induced contractions and calcium regulation is also energy dependent. Myocytes have an abundance of mitochondria and significant heme-protein requirements to help transport oxygen to mitochondria and supply energy. In myocytes, the mitochondria are uniquely co-localized with the endoplasmic reticulum, where calcium stores are regulated. My research program seeks to understand: 1) how mitochondrial function affects the production of heme, 2) how heme, or the need for heme, affects contractility and vice versa, 3) the key mechanisms and proteins that regulate a myocyte's complex demands for heme, energy, and tightly regulated calcium stores. Using chemical and genetic methods, we will manipulate the amount of heme formed in myocytes under different biological states including: sympathetic drive, stretch and hypoxia. We will determine how heme synthesis impacts calcium stores in the mitochondria and endoplasmic reticulum. Then we will seek out the molecular mechanisms, such as DNA binding transcription factors that regulate heme homeostasis in myocytes. The research we will conduct will help train new HQP in many techniques like: cell culture, protein chemistry, muscle physiology and genetics, flow cytometry, whole muscle function analysis, calcium measurements and intracellular organelle labeling. These studies will be important for understanding how heme metabolism and biological demands are coordinated. These findings would provide important new information for textbooks and have a significant impact in our understanding basic cell functions.