Single-cell profiling of immune system alterations in lymphoid, barrier and solid tissues in aged mice

Inflammation Mammals Aging 0303 health sciences Neuroscience (miscellaneous) 610 Medicine & health 2717 Geriatrics and Gerontology 10263 Institute of Experimental Immunology Flow Cytometry 3. Good health Killer Cells, Natural Mice 03 medical and health sciences 1302 Aging Phenotype 2801 Neuroscience (miscellaneous) Phagocytosis 570 Life sciences; biology Animals Geriatrics and Gerontology
DOI: 10.1038/s43587-021-00148-x Publication Date: 2021-12-16T17:05:43Z
ABSTRACT
Aging exerts profound and paradoxical effects on the immune system, at once impairing proliferation, cytotoxicity and phagocytosis, and inducing chronic inflammation. Previous studies have focused on individual tissues or cell types, while a comprehensive multisystem study of tissue-resident and circulating immune populations during aging is lacking. Here we reveal an atlas of age-related changes in the abundance and phenotype of immune cell populations across 12 mouse tissues. Using cytometry-based high parametric analysis of 37 mass-cytometry and 55 spectral flow-cytometry parameters, mapping samples from young and aged animals revealed conserved and tissue-type-specific patterns of both immune atrophy and expansion. We uncovered clear phenotypic changes in both lymphoid and myeloid lineages in aged mice, and in particular a contraction in natural killer cells and plasmacytoid dendritic cells. These changes correlated with a skewing towards myelopoiesis at the expense of early lymphocyte genesis in aged mice. Taken together, this atlas represents a comprehensive, systematic and thorough resource of the age-dependent alterations of the mammalian immune system in lymphoid, barrier and solid tissues.
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