Author
Listed:
- Jacob M. Stillman
(University of Massachusetts Chan Medical School
University of Massachusetts Chan Morningside Graduate School of Biomedical Sciences, Neuroscience Program)
- Francisco Mendes Lopes
(University of Massachusetts Chan Medical School)
- Jing-Ping Lin
(Translational Neuroradiology Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health)
- Kevin Hu
(Translational Neuroradiology Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health)
- Daniel S. Reich
(Translational Neuroradiology Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health)
- Dorothy P. Schafer
(University of Massachusetts Chan Medical School)
Abstract
Engulfment of cellular material and proteins is a key function for microglia, a resident macrophage of the central nervous system (CNS). Among the techniques used to measure microglial engulfment, confocal light microscopy has been used the most extensively. Here, we show that autofluorescence (AF) likely due to lipofuscin (lipo-AF) and typically associated with aging, can also be detected within microglial lysosomes in the young mouse brain by light microscopy. This lipo-AF signal accumulates first within microglia and it occurs earliest in white versus gray matter. Importantly, in gray matter, lipo-AF signal can confound the interpretation of antibody-labeled synaptic material within microglia in young adult mice. We further show that there is an age-dependent accumulation of lipo-AF inside and outside of microglia, which is not affected by amyloid plaques. We finally implement a robust and cost-effective strategy to quench AF in mouse, marmoset, and human brain tissue.
Suggested Citation
Jacob M. Stillman & Francisco Mendes Lopes & Jing-Ping Lin & Kevin Hu & Daniel S. Reich & Dorothy P. Schafer, 2023.
"Lipofuscin-like autofluorescence within microglia and its impact on studying microglial engulfment,"
Nature Communications, Nature, vol. 14(1), pages 1-11, December.
Handle:
RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42809-y
DOI: 10.1038/s41467-023-42809-y
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