Published December 2021 | Version v1
Journal article

Aging-associated stem/progenitor cell dysfunction in the salivary glands of mice

  • 1. Division of Pathology, Department of Oral Diagnostic Sciences, School of Dentistry, Showa University, Tokyo (Japan)
  • 2. Department of Oral and Maxillofacial Surgery, School of Dentistry, Showa University, Tokyo (Japan)
  • 3. Department of Systems Aging Science and Medicine, Tokyo Metropolitan Institute of Gerontology, Tokyo (Japan)
  • 4. Department of Dentistry, Jikei University School of Medicine, Tokyo (Japan)
  • 5. Department of Oral Medicine, Tokushima University Graduate School of Biomedical Sciences, Tokushima (Japan)
  • 6. Division of Gene Regulation and Signal Transduction, Research Center of Genomic Medicine, Saitama Medical University, Saitama (Japan)

Description

Highlights: • The function of CD133-positive cells changes with age and is expected to be one of the causative factors associated with salivary gland aging. Although stem cell aging leads to a decline in tissue homeostasis and regenerative capacity, it remains unclear whether salivary gland stem cell function changes during this process. However, the salivary glands are gradually replaced by connective tissue during aging. Here, we show a decline in the stem cell ability of CD133-positive stem/progenitor cells in the salivary glands of aged mice. The CD133-positive cells were isolated from young, adult, and aged mice. The number of CD133-positive cells was significantly decreased in aged mice. They also showed a lower sphere formation capacity compared to young and adult mice. RNA sequencing revealed that CD133-positive cells in aged mice exhibited lower gene expression of several aging-related genes, including FoxO3a, than those in young and adult mice. Salivary gland cells infected with a recombinant lentivirus encoding the FoxO3a gene showed a reduction in oxidative stress induced by hydrogen peroxide compared with those infected with a control virus. Thus, FoxO3a may inhibit stem cell aging via oxidative stress.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.yexcr.2021.112889

Additional details

Identifiers

DOI
10.1016/j.yexcr.2021.112889;
PII
S0014482721004432;

Publishing Information

Journal Title
Experimental Cell Research
Journal Volume
409
Journal Issue
1
Journal Page Range
vp.
ISSN
0014-4827
CODEN
ECREAL

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
53119056
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
CONNECTIVE TISSUE; HOMEOSTASIS; HYDROGEN PEROXIDE; MICE; OXIDATION; RNA; SALIVARY GLANDS; STEM CELLS; VIRUSES
Descriptors DEC
ANIMAL CELLS; ANIMAL TISSUES; ANIMALS; BODY; CHEMICAL REACTIONS; GLANDS; HYDROGEN COMPOUNDS; MAMMALS; MICROORGANISMS; NUCLEIC ACIDS; ORGANIC COMPOUNDS; ORGANS; OXYGEN COMPOUNDS; PARASITES; PEROXIDES; RODENTS; SOMATIC CELLS; VERTEBRATES

Optional Information

Copyright
Copyright (c) 2021 Elsevier Inc. All rights reserved.