Aging disrupts hepatocyte zonation homeostasis in mice and humans.
Abstract
Aging-induced degenerative changes in the liver are not inherently pathologic but pose an increased risk for liver diseases. However, the molecular mechanisms underlying aging-induced hepatic dyshomeostasis remain incompletely characterized. Here, we investigate how aging alters liver architecture, cellular communication, and hepatocyte zonation.
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Research summary
Aging disrupts hepatocyte zonation homeostasis in the liver. The paper addresses the molecular mechanisms of aging-related changes in liver architecture, which is crucial for understanding the root causes of aging and potential interventions.
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