Tanguay Adam P, Menon Nikhil G, Slavin Emma, Moody Mikayla, McEwen Erin, Jay Gregory D, Lorenzo Joseph, Bartley Jenna M, Scanlon Vanessa M, Deymier Alix C, Schmidt Tannin A
Biomedical Engineering Department, UConn Health, Farmington, CT, USA.
Center for Regenerative Medicine and Skeletal Development, UConn Health, Farmington, CT, USA.
Geroscience. 2025 Jun 19. doi: 10.1007/s11357-025-01747-x.
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.
蛋白聚糖4(PRG4)是一种黏蛋白样糖蛋白,最为人所知的是它作为关节软骨的边界润滑剂;然而,它也具有抗炎、抗纤维化和免疫调节特性。人类PRG4基因的功能丧失突变会导致先天性屈曲指-关节病-髋内翻-心包炎(CACP),这是一种罕见疾病,患者通常在年轻时就需要进行关节置换。然而,目前尚不清楚循环PRG4水平如何随年龄变化,以及PRG4缺乏如何影响衰老。因此,本研究的首要目标是测量年轻和老年野生型(WT)小鼠的血清PRG4水平。我们发现老年WT小鼠的血清PRG4浓度低于年轻小鼠。接下来,我们评估了PRG4缺乏对生存的影响,确定Prg4基因陷阱(GT,PRG4缺乏)小鼠的生存概率低于WT小鼠。最后,我们研究了PRG4缺乏如何影响中年Prg4 GT小鼠的血气、全血细胞计数和骨骼。与WT小鼠相比,Prg4 GT小鼠的各种血液参数发生了改变,并表现出性别差异。PRG4缺乏在性别上依赖地降低了中年小鼠骨骼的小梁和皮质特性,衰老和基因型表现出与雄性骨骼加速衰老一致的相互作用效应。总体而言,本研究初步探讨了WT小鼠血清PRG4水平随年龄的变化以及PRG4缺乏在衰老过程中的影响。这些发现为未来的研究奠定了基础,以便从机制上扩展这项工作,并评估其在CACP和老年人群中的临床相关性。