Cellular accumulation of lipofuscin in the heart: implications in health and disease

Lipofuscin is a subcellular pigmented granule that has long been considered a sign of wear-and-tear and aging. This granule cannot be degraded but may be diluted by cell division. In the heart, lipofuscin can be easily identified in cardiomyocytes where proliferative capacity is limited, and to a lesser extent in other cardiac cell types, by their characteristic morphological features. They appear as yellow-brown granules in histopathology sections reflecting their lipid origins, and as heterogenous membrane-bound bodies containing a mix of lipid and electron-lucent content in transmission electron microscopy. Lipofuscin was originally considered a mere byproduct of age-related cell senescence but studies over the past three decades have indicated that its role and mechanism of formation may be far more complex. In this review, we examine how lipofuscin is formed and its implications in aging and diseases of the heart. While the focus of this review is on lipofuscin in the two most predominate cell types of the heart, cardiomyocytes and fibroblasts, we also touch on the presence of lipofuscin in the vasculature in certain disease phenotypes that are directly relevant to cardiovascular health.

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Publication Details

Journal
Histochemistry and Cell Biology
Published
2026-06-25
DOI
https://doi.org/10.1007/s00418-026-02501-w
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
0.00

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article

Cellular accumulation of lipofuscin in the heart: implications in health and disease

Filip Braet, Kenneth S. Campbell, Amy Li, Sean Lal et al.
Histochemistry and Cell Biology
Mitochondrial Function and Pathology
article

Cellular accumulation of lipofuscin in the heart: implications in health and disease

Filip Braet, Kenneth S. Campbell, Amy Li, Sean Lal, Gerald J. Shami, Eddie Wisse
article en

Abstract

Lipofuscin is a subcellular pigmented granule that has long been considered a sign of wear-and-tear and aging. This granule cannot be degraded but may be diluted by cell division. In the heart, lipofuscin can be easily identified in cardiomyocytes where proliferative capacity is limited, and to a lesser extent in other cardiac cell types, by their characteristic morphological features. They appear as yellow-brown granules in histopathology sections reflecting their lipid origins, and as heterogenous membrane-bound bodies containing a mix of lipid and electron-lucent content in transmission electron microscopy. Lipofuscin was originally considered a mere byproduct of age-related cell senescence but studies over the past three decades have indicated that its role and mechanism of formation may be far more complex. In this review, we examine how lipofuscin is formed and its implications in aging and diseases of the heart. While the focus of this review is on lipofuscin in the two most predominate cell types of the heart, cardiomyocytes and fibroblasts, we also touch on the presence of lipofuscin in the vasculature in certain disease phenotypes that are directly relevant to cardiovascular health.

Histochemistry and Cell BiologyVol. 164(1)
The University of Sydney (AU), University of Kentucky (US), La Trobe University (AU), Maastricht University (NL), Torrens University Australia (AU)
American Heart Association, University of Sydney, National Institutes of Health, Larner College of Medicine, University of Vermont
Good health and well-being
Openalex Percentile: Top 11%
Mitochondrial Function and Pathology
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