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Geroscience. 2018 Jun;40(3):279-291. doi: 10.1007/s11357-018-0022-2. Epub 2018 May 26.

Calorie restriction induces reversible lymphopenia and lymphoid organ atrophy due to cell redistribution.

Author information

1
Department of Immunobiology, College of Medicine, The University of Arizona, Tucson, AZ, USA.
2
Division of Geriatrics and Nutritional Science, Washington University School of Medicine, St. Louis, MO, USA. lfontana@wustl.edu.
3
Department of Experimental and Clinical Sciences, Brescia University, Brescia, Italy. lfontana@wustl.edu.
4
Division of Geriatrics and Nutritional Science, Washington University School of Medicine, St. Louis, MO, USA.
5
Department of Immunobiology, College of Medicine, The University of Arizona, Tucson, AZ, USA. nikolich@email.arizona.edu.
6
Arizona Center on Aging, College of Medicine, The University of Arizona, Tucson, AZ, USA. nikolich@email.arizona.edu.

Abstract

Calorie restriction (CR) without malnutrition increases life span and health span in multiple model organisms. In non-human and human primates, CR causes changes that protect against several age-related pathologies, reduces inflammation, and preserves or improves cell-mediated immunity. However, CR has also been shown to exhibit adverse effects on certain organs and systems, including the immune system, and to impact genetically different organisms of the same species differentially. Alternately, short periods of fasting followed by refeeding may result in the proliferation of bone marrow stem cells, suggesting a potential rejuvenation effect that could impact the hematopoietic compartment. However, the global consequences of CR followed by refeeding on the immune system have not been carefully investigated. Here, we show that individuals practicing long-term CR with adequate nutrition have markedly lower circulating levels of total leukocytes, neutrophils, lymphocytes, and monocytes. In 10-month-old mice, short-term CR lowered lymphocyte cellularity in multiple lymphoid tissues, but not in bone marrow, which appears to be a site of influx, or a "safe haven" for B, NK, and T cells during CR. Cellular loss and redistribution was reversed within the first week of refeeding. Based on BrdU incorporation and Ki67 expression assays, repopulating T cells exhibited high proliferation in the refeeding group following CR. Finally, we demonstrated that the thymus was not essential for T cell repopulation following refeeding. These findings are of potential relevance to strategies to rejuvenate the immune system in mammals and warrant further investigation.

KEYWORDS:

Aging; Calorie restriction; Cellular immunology; Leukocytes; Lymphocytes; Rejuvenation

PMID:
29804201
PMCID:
PMC6060198
DOI:
10.1007/s11357-018-0022-2
[Indexed for MEDLINE]
Free PMC Article

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