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Published on: February 25, 2014
Proteoglycan-4 (PRG4) serum concentration is lower in aged mice, and genetic deficiency impacts survival probability,
Adam P Tanguay1, Nikhil G Menon1, Emma Slavin1
1Biomedical Engineering Department, UConn Health, Farmington, CT, USA.
Abstract:
Proteoglycan 4 (PRG4) is a mucin-like glycoprotein best known as a boundary lubricant of articular cartilage; however, it also has anti-inflammatory, anti-fibrotic, and immunomodulatory properties. Loss-of-function mutations in the PRG4 gene in humans result in Camptodactyly-Arthropathy-Coxa vara-Pericarditis (CACP), a rare disease in which patients often require joint replacements at young ages. However, it remains unknown how circulating PRG4 levels change with age or how PRG4 deficiency affects aging. Therefore, the first objective of this study was to measure serum PRG4 levels in young and aged wild type (WT) mice. We found that serum PRG4 concentration was lower in aged than young WT mice. Next, we assessed the impact of PRG4 deficiency on survival and determined that Prg4 gene trap (GT, PRG4 deficient) mice had lower survival probability than WT mice. Finally, we examined how PRG4 deficiency impacts blood gases, complete blood counts, and bone in middle-aged Prg4 GT mice. Various blood parameters were altered in Prg4 GT mice versus WT and exhibited sexual dimorphism. PRG4 deficiency diminished trabecular and cortical properties of bone in middle-aged mice sex-dependently, and aging and genotype exhibited an interaction effect consistent with accelerated skeletal aging in males. Overall, this study provides an initial examination into changes in serum PRG4 levels with age in WT mice as well as the effect of PRG4 deficiency in aging. These findings pave the way for future studies to expand on this work mechanistically and assess clinical relevance in CACP and in aging populations.
Insights
Serum proteoglycan 4 (PRG4) levels decrease with age. PRG4 deficiency accelerates aging, impacting survival, blood parameters, and bone health, particularly in male mice.
Area of Science:
- Biochemistry
- Gerontology
- Rheumatology
Background:
- Proteoglycan 4 (PRG4) is a key lubricant in joints with known anti-inflammatory and immunomodulatory roles.
- PRG4 gene mutations cause Camptodactyly-Arthropathy-Coxa vara-Pericarditis (CACP), leading to early joint replacement.
- The impact of aging on PRG4 levels and the consequences of PRG4 deficiency in aging remain largely unexplored.
Purpose of the Study:
- To investigate age-related changes in serum PRG4 levels in wild-type (WT) mice.
- To evaluate the effect of PRG4 deficiency on survival and aging phenotypes in mice.
- To analyze how PRG4 deficiency impacts blood parameters and bone structure in aging mice.
Main Methods:
- Serum PRG4 concentrations were measured in young and aged WT mice.
- Survival rates of Prg4 gene trap (GT) mice and WT mice were compared.
- Blood gases, complete blood counts, and bone properties (trabecular and cortical) were assessed in middle-aged Prg4 GT mice and WT controls.
Main Results:
- Serum PRG4 levels were significantly lower in aged WT mice compared to young WT mice.
- Prg4 GT mice exhibited reduced survival probability compared to WT mice.
- PRG4 deficiency altered blood parameters with sexual dimorphism and diminished bone properties, indicating accelerated skeletal aging in male Prg4 GT mice.
Conclusions:
- Aging is associated with decreased serum PRG4 levels.
- PRG4 deficiency negatively impacts survival and accelerates aging phenotypes, including skeletal deterioration, with sex-specific effects.
- These findings highlight PRG4's role in aging and suggest potential therapeutic targets for CACP and age-related conditions.
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