The age-dependent influence of the infrapatellar fat pad on chondrocyte extracellular matrix production.

Ella D'Amico,Tyler J McNeill,Adam M Khay,Gabrielle Gilmer,Kai Wang,Juliana Bergmann,Amrita Sahu,Hirotaka Iijima,Fabrisia Ambrosio
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Abstract

Despite the growing burden of knee osteoarthritis (KOA) on aging populations, our mechanistic understanding of this disease remains lacking. Though KOA is a whole joint disease, the impact of intra-articular structures, like the infrapatellar fat pad (IFP), on cartilage health is unclear. This study investigated the effect of age on paracrine communication between IFPs and chondrocytes. To isolate the effects of the IFP secretome on chondrocytes, aged chondrocytes from male and female mice were incubated with conditioned media from sex-matched young IFPs, aged IFPs, or control media. ECM protein expression increased in both male and female chondrocytes exposed to young, but not aged, conditioned media relative to control media. The effect of the young IFP was not concomitant with changes in ECM degradation proteins, ADAMTS4 or MMP13. To identify factors mediating the effects of the IFP on chondrocytes that are altered with aging, we performed mass spectrometry of young and aged conditioned media and transcriptomics of aged chondrocytes treated with this media. We then integrated the two datasets using network analyses. From the conditioned media, two secreted proteins, Mfge8 and Apoa4, were significantly changed with aging. In silico perturbation of the corresponding receptors of these IFP-secreted factors identified multiple enriched pathways, including negative regulation of nitric oxide synthase activity, in chondrocytes. Overall, the data suggest that young IFPs release paracrine factors that promote ECM production in chondrocytes, potentially via regulation of nitric oxide levels, but that this effect is diminished with aging.
髌下脂肪垫对软骨细胞细胞外基质生成的年龄依赖性影响。
尽管膝关节骨关节炎(KOA)对老年人的负担越来越重,但我们对这种疾病的机制理解仍然缺乏。虽然KOA是一种全关节疾病,但关节内结构,如髌下脂肪垫(IFP)对软骨健康的影响尚不清楚。本研究探讨了年龄对IFPs与软骨细胞间分泌旁通讯的影响。为了分离IFP分泌组对软骨细胞的影响,将雄性和雌性小鼠的衰老软骨细胞与性别匹配的年轻IFP、老年IFP或对照培养基孵育。与对照培养基相比,暴露于年轻而非衰老条件培养基中的男性和女性软骨细胞的ECM蛋白表达均有所增加。年轻IFP的作用不伴随ECM降解蛋白ADAMTS4或MMP13的变化。为了确定介导IFP对随年龄变化的软骨细胞的影响的因素,我们对年轻和老年条件培养基进行了质谱分析,并对用该培养基处理的老年软骨细胞进行了转录组学分析。然后,我们使用网络分析整合了两个数据集。在条件培养基中,两种分泌蛋白Mfge8和Apoa4随着年龄的增长而显著改变。通过对这些ifp分泌因子的相应受体的微扰,确定了软骨细胞中多种富集途径,包括一氧化氮合酶活性的负调控。总的来说,数据表明年轻的ifp释放副分泌因子,促进软骨细胞中ECM的产生,可能通过调节一氧化氮水平,但这种作用随着年龄的增长而减弱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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