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.

Geroscience
|June 19, 2025
PubMed

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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