Abstract

In C. elegans, intestinal autofluorescence (sometimes referred to as lipofuscin or “age pigment”) accumulates with age and is often used as a marker of health or the rate of aging. We show that this autofluorescent material is spectrally heterogeneous, and that materials that fluoresce under different excitation wavelengths have distinct biological properties. Red autofluorescence (visible with a TRITC filterset) correlates well with an individual's remaining days of life, and is therefore a candidate marker of health. In contrast, blue autofluorescence (via a DAPI filterset) is chiefly an indicator of an individual's incipient or recent demise. Thus, population averages of blue fluorescence essentially measure the fraction of dead or near-dead individuals. This is related to but distinct from the health of the living population. Green autofluorescence (via a FITC or GFP filterset) combines both properties, and is therefore ill suited as a marker of either death or health. Moreover, our results show that care must be taken to distinguish GFP expression near the time of death from full-body green autofluorescence. Finally, none of this autofluorescence increases after oxidative stress, suggesting that the material, or its biology in C. elegans, is distinct from lipofuscin as reported in the mammalian literature.

Highlights

  • Autofluorescent material builds up over time in cells and tissues with low turnover, and is often used as a marker of cellular and even organismal aging [1]

  • In C. elegans, as in mammalian cells, much of the autofluorescence is confined to intracellular granules of lysosomal origin, which, in C. elegans, are generally found within intestinal cells [15]

  • We find that autofluorescent material in C. elegans is spectrally and biologically more complex than previously understood

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Summary

Introduction

Autofluorescent material builds up over time in cells and tissues with low turnover, and is often used as a marker of cellular and even organismal aging [1]. This material, first described almost 175 years ago [2], is generically described as “age pigment” or lipofuscin, and has been characterized extensively in many different organisms [3,4,5,6,7,8,9]. The precise relationship between autofluorescence, aging, and lifespan in C. elegans has remained somewhat ill defined, . Different groups have come to different conclusions regarding whether autofluorescence in particular wavelengths does [16] or does not [17] increase with age as a reflection of the overall health of a population of animals, and whether autofluorescence in a particular www.impactaging.com

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