Senescence-accelerated mice (SAMs) as a model for brain aging and immunosenescence

Atsuyoshi Shimada, Sanae Hasegawa-Ishii

Research output: Contribution to journalReview article

26 Citations (Scopus)

Abstract

The Senescence-Accelerated Mouse (SAM) represents a group of inbred mouse strains developed as a model for the study of human aging and age-related diseases. Senescence-prone (SAMP) strains exhibit an early onset of age-related decline in the peripheral immunity such as thymic involution, loss of CD4+ T cells, impaired helper T cell function, decreased antibody-forming capacity, dysfunction of antigen-presenting cells, decreased natural killer activity, increased auto-antibodies, and susceptibility to virus infection. Senescence-prone SAMP10 mice undergo age-related changes in the brain such as brain atrophy, shrinkage and loss of cortical neurons, retraction of cortical neuronal dendrites, loss of dendritic spines, loss of synapses, impaired learning and memory, depressive behavior, accumulation of neuronal DNA damage, neuronal ubiquitinated inclusions, reduced hippocampal cholinergic receptors, decreased neurotrophic factors, decreased hippocampal zinc and zinc transporters, increased sphyngomyelinase, and elevated oxidative-nitrative stress. Recent data indicating increased pro-inflammatory cytokines in the brain of SAMP10 mice are directing investigators toward an integration of immune and neural abnormalities to enhance understanding of the principles of brain aging. We highlight how mouse brain cells adopt cytokine-mediated responses and how SAMP10 mice are defective in these responses. SAMP10 model would be useful to study how age-related disturbances in peripheral immunity have an impact on dysregulation of brain tissue homeostasis, resulting in age-related neurodegeneration.

Original languageEnglish (US)
Pages (from-to)414-436
Number of pages23
JournalAging and Disease
Volume2
Issue number5
StatePublished - Jan 1 2011

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Brain
Immunity
Cytokines
Dendritic Spines
Inbred Strains Mice
Antibodies
Nerve Growth Factors
Cholinergic Receptors
Antigen-Presenting Cells
Virus Diseases
Dendrites
Helper-Inducer T-Lymphocytes
Age of Onset
Synapses
DNA Damage
Atrophy
Immunosenescence
Zinc
Oxidative Stress
Homeostasis

All Science Journal Classification (ASJC) codes

  • Pathology and Forensic Medicine
  • Geriatrics and Gerontology
  • Clinical Neurology
  • Cell Biology

Cite this

Shimada, Atsuyoshi ; Hasegawa-Ishii, Sanae. / Senescence-accelerated mice (SAMs) as a model for brain aging and immunosenescence. In: Aging and Disease. 2011 ; Vol. 2, No. 5. pp. 414-436.
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Shimada, A & Hasegawa-Ishii, S 2011, 'Senescence-accelerated mice (SAMs) as a model for brain aging and immunosenescence', Aging and Disease, vol. 2, no. 5, pp. 414-436.

Senescence-accelerated mice (SAMs) as a model for brain aging and immunosenescence. / Shimada, Atsuyoshi; Hasegawa-Ishii, Sanae.

In: Aging and Disease, Vol. 2, No. 5, 01.01.2011, p. 414-436.

Research output: Contribution to journalReview article

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