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Isolation of Intermediate Filament Proteins from Multiple Mouse Tissues to Study Aging-associated Post-translational Modifications
Published on: May 18, 2017
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Age-associated decrease of senescence marker protein-30/gluconolactonase in individual mouse liver cells:
Akihito Ishigami1, Hirofumi Masutomi1, Setsuko Handa1
1Molecular Regulation of Aging, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.
Geriatrics & Gerontology International
|October 15, 2014
Summary
Senescence marker protein-30 (SMP30)/gluconolactonase (GNL) protein decreases in mouse liver cells with aging. This age-associated protein, found in nuclei and cytoplasm, may regulate gene expression and the aging process.
Area of Science:
- Gerontology
- Cell Biology
- Hepatology
Background:
- Senescence marker protein-30 (SMP30)/gluconolactonase (GNL) is an age-associated protein that declines with aging.
- Investigating SMP30/GNL changes in liver cells provides insights into cellular aging mechanisms.
Purpose of the Study:
- To investigate age-related changes in SMP30/GNL expression within individual mouse liver cells.
- To determine the cellular localization and distribution of SMP30/GNL in aging mouse livers.
Main Methods:
- Immunohistochemical analysis of liver sections from mice aged 1 to 30 months.
- Immunofluorescent staining of primary cultured hepatocytes for SMP30/GNL and albumin.
Main Results:
- SMP30/GNL staining was observed in both the nuclei and cytoplasm of some parenchymal cells, primarily around central veins.
- The number of SMP30/GNL-positive cells increased from 1 to 12 months and then decreased from 12 to 24 months of age.
- No age-related changes were observed in albumin-positive cell counts.
Conclusions:
- SMP30/GNL-positive cells are concentrated around central veins and decrease in number with aging.
- Nuclear SMP30/GNL protein may play a role in regulating gene expression involved in transcription and aging.
- SMP30/GNL serves as a potential biomarker for cellular aging in the liver.

