Friday, May 9, 2025
5/9/2025
PPARgamma Coregulators in Rosiglitazone-Induced Cardiovascular Disease - Summary Rosiglitazone (Rosi) treats type 2 diabetes (T2D) and effectively lowers blood glucose via the nuclear receptor PPARγ activation. Rosi has been reduced in use due to it inducing congestive heart failure (CHF). PPARγ is a ligand-activated transcription factor that is highly expressed in adipose tissues and, to a lesser extent, in cardiac tissue. It is regulated through various mechanisms, like coregulators that physically interact with PPARγ to activate or repress its transcriptional activity. Hence, the PPARγ-interactome regulates functions that drive it toward genes that control specific pathways. My goal for this project is to determine the global genome view of the heart and adipose tissue during Rosi activation of PPARγ that leads to the deleterious effects associated with the drug. We will investigate if the PPARγ interactome changes based on diet (high-fat versus chow diets) and whether this guides the transcription factor to specific PPAR-response elements (PPREs) in gene promoters inducing specific pathways. These concepts have led to the central hypothesis that chronic high-fat feeding in the obese causes a change in the PPARγ interactome and pathways controlled by the transcription factor that leads to cardiac dysfunction. We will measure these in the following aims: Aim 1: We hypothesize that high-fat (HFD) feeding alters PPARγ-directed pathways in the heart, causing a switch in gene regulatory actions and cardiac steatosis. Aim 2: We hypothesize that PPARγ activation in adipose tissue of chronically obese mice activates inflammatory hormones that cause cardiac dysfunction. To measure these, we will use our state-of- the-art PamGene PamStation to measure the PPARγ coregulator interactome, RNA-sequencing, and PPARγ chromatin immunoprecipitation (ChIP)-seq in adipose and heart tissues in the mice described above. We expect to find that chronic high-fat feeding changes the PPARγ coregulator interactome, driving it to pathways that lead to deleterious outcomes, such as our finding that Serpine1 mRNA (plasminogen activator inhibitor 1, PAI-1 protein) levels were increased in the HFD Rosi, but not in normal chow mice with Rosi treatments. PAI-1 is involved in cardiovascular disease, but nothing is known about its role in PPARγ-induced CHF. Our studies here will improve the understanding of PPARγ in cardiac function and possibly provide methods of treating persons who experience CHF.
HHS’ Tracking Accountability in Government Grants System (TAGGS) website provides access to detailed descriptions of grants, loans, aggregated direct payments and other types of financial assistance awarded by the HHS Operating Divisions (OPDIVs) and the Office of the Secretary Staff Divisions (STAFFDIVs).