• Open Access

Age-associated increase in heterochromatic marks in murine and primate tissues

Authors


John M. Sedivy, Department of Molecular Biology, Cell Biology and Biochemistry, Laboratories for Molecular Medicine, 70 Ship Street, Providence, RI 02903, USA. Tel.: +401 863 7631; fax: +401 863 9653; e-mail: john_sedivy@brown.edu
or

Jill A. Kreiling, Department of Molecular Biology, Cell Biology and Biochemistry, Laboratories for Molecular Medicine, 70 Ship Street, Providence, RI 02903, USA. Tel.: +401 863-7674; fax: +401 863 9653; e-mail: jill_kreiling@brown.edu

Summary

Chromatin is highly dynamic and subject to extensive remodeling under many physiologic conditions. Changes in chromatin that occur during the aging process are poorly documented and understood in higher organisms, such as mammals. We developed an immunofluorescence assay to quantitatively detect, at the single cell level, changes in the nuclear content of chromatin-associated proteins. We found increased levels of the heterochromatin-associated proteins histone macro H2A (mH2A) and heterochromatin protein 1 beta (HP1β) in human fibroblasts during replicative senescence in culture, and for the first time, an age-associated increase in these heterochromatin marks in several tissues of mice and primates. Mouse lung was characterized by monophasic mH2A expression histograms at both ages, and an increase in mean staining intensity at old age. In the mouse liver, we observed increased age-associated localization of mH2A to regions of pericentromeric heterochromatin. In the skeletal muscle, we found two populations of cells with either low or high mH2A levels. This pattern of expression was similar in mouse and baboon, and showed a clear increase in the proportion of nuclei with high mH2A levels in older animals. The frequencies of cells displaying evidence of increased heterochromatinization are too high to be readily accounted for by replicative or oncogene-induced cellular senescence, and are prominently found in terminally differentiated, postmitotic tissues that are not conventionally thought to be susceptible to senescence. Our findings distinguish specific chromatin states in individual cells of mammalian tissues, and provide a foundation to investigate further the progressive epigenetic changes that occur during aging.

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