Ceramides are signals of fatty acid excess that accumulate when a cell's energetic needs have been met and its nutrient storage has reached capacity. As these sphingolipids accrue, they alter the metabolism and survival of cells throughout the body including in the heart, liver, blood vessels, skeletal muscle, brain, and kidney. These ceramide actions elicit the tissue dysfunction that underlies cardiometabolic diseases such as diabetes, coronary artery disease, metabolic-associated steatohepatitis, and heart failure. Here, we review the biosynthesis and degradation pathways which maintain ceramide levels in normal physiology and discuss how the loss of ceramide homeostasis drives cardiometabolic pathologies. We highlight signaling nodes that sense small changes in ceramides, and in turn reprogram cellular metabolism and stimulate apoptosis. Lastly, we evaluate the emerging therapeutic utility of these unique lipids as biomarkers that forecast disease risk and as targets of ceramide-lowering interventions that ameliorate disease.
Keyphrases
- heart failure
- coronary artery disease
- skeletal muscle
- fatty acid
- cell cycle arrest
- induced apoptosis
- type diabetes
- cardiovascular disease
- endoplasmic reticulum stress
- atrial fibrillation
- physical activity
- cardiovascular events
- stem cells
- cell death
- insulin resistance
- single cell
- sensitive detection
- coronary artery bypass grafting
- multiple sclerosis
- radiation therapy
- white matter
- percutaneous coronary intervention
- glycemic control
- left ventricular
- signaling pathway
- quantum dots
- blood brain barrier
- cell proliferation
- lymph node
- pi k akt
- single molecule
- brain injury
- rectal cancer