Disentangling the detrimental effects of local from systemic adipose tissue dysfunction on articular cartilage in the knee

IF 7.2 2区 医学 Q1 ORTHOPEDICS Osteoarthritis and Cartilage Pub Date : 2024-08-03 DOI:10.1016/j.joca.2024.07.006
Jessica J. McClure , George D. McIlroy , Rebecca A. Symons , Susan M. Clark , Iain Cunningham , Weiping Han , Karolina Kania , Fabio Colella , Justin J. Rochford , Cosimo De Bari , Anke J. Roelofs
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Abstract

Objective

Obesity increases osteoarthritis (OA) risk due to adipose tissue dysfunction with associated metabolic syndrome and excess weight. Lipodystrophy syndromes exhibit systemic metabolic and inflammatory abnormalities similar to obesity without biomechanical overloading. Here, we used lipodystrophy mouse models to investigate the effects of systemic versus intra-articular adipose tissue dysfunction on the knee.

Methods

Intra-articular adipose tissue development was studied using reporter mice. Mice with selective lipodystrophy of intra-articular adipose tissue were generated by conditional knockout (cKO) of Bscl2 in Gdf5-lineage cells, and compared with whole-body Bscl2 knockout (KO) mice with generalised lipodystrophy and associated systemic metabolic dysfunction. OA was induced by surgically destabilising the medial meniscus (DMM) and obesity by high-fat diet (HFD). Gene expression was analysed by quantitative RT-PCR and tissues were analysed histologically.

Results

The infrapatellar fat pad (IFP), in contrast to overlying subcutaneous adipose tissue, developed from a template established from the Gdf5-expressing joint interzone during late embryogenesis, and was populated shortly after birth by adipocytes stochastically arising from Pdgfrα-expressing Gdf5-lineage progenitors. While female Bscl2 KO mice with generalised lipodystrophy developed spontaneous knee cartilage damage, Bscl2 cKO mice with intra-articular lipodystrophy did not, despite the presence of synovial hyperplasia and inflammation of the residual IFP. Furthermore, male Bscl2 cKO mice showed no worse cartilage damage after DMM. However, female Bscl2 cKO mice showed increased susceptibility to the cartilage-damaging effects of HFD-induced obesity.

Conclusion

Our findings emphasise the prevalent role of systemic metabolic and inflammatory effects in impairing cartilage homeostasis, with a modulatory role for intra-articular adipose tissue.
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厘清局部和全身脂肪组织功能障碍对膝关节软骨的有害影响。
目的:肥胖会增加骨关节炎(OA)的风险,这是由于脂肪组织功能障碍以及相关的代谢综合征和超重造成的。脂肪营养不良综合征表现出与肥胖相似的全身代谢和炎症异常,但没有生物力学超负荷。在此,我们使用脂肪营养不良小鼠模型来研究全身与关节内脂肪组织功能障碍对膝关节的影响:方法:使用报告小鼠研究关节内脂肪组织的发育情况。通过条件性敲除(cKO)Gdf5系细胞中的Bscl2,产生了关节内脂肪组织选择性脂肪营养不良的小鼠,并与患有全身性脂肪营养不良和相关全身代谢功能障碍的先天性Bscl2 KO小鼠进行了比较。通过手术破坏内侧半月板(DMM)和高脂饮食(HFD)诱发肥胖。通过定量 RT-PCR 分析基因表达,并对组织进行组织学分析:结果:与上覆皮下脂肪组织不同,髌下脂肪垫(IFP)是在胚胎发育晚期从Gdf5表达的关节间区建立的模板上发育而成的,并在出生后不久由Pdgfrα+ Gdf5系祖细胞随机产生的脂肪细胞填充。患有全身性脂肪营养不良症的雌性 Bscl2 KO 小鼠会出现自发性膝关节软骨损伤,而患有关节内脂肪营养不良症的 Bscl2 cKO 小鼠尽管出现了滑膜增生和残余 IFP 的炎症,却没有出现膝关节软骨损伤。此外,雄性 Bscl2 cKO 小鼠在 DMM 后没有出现更严重的软骨损伤。然而,患有关节内脂肪营养不良症的雌性Bscl2 cKO小鼠对HFD诱导的肥胖造成的软骨损伤效应表现出更高的易感性:我们的研究结果强调了全身代谢和炎症效应在损害软骨稳态中的普遍作用,以及关节内脂肪组织的调节作用。
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来源期刊
Osteoarthritis and Cartilage
Osteoarthritis and Cartilage 医学-风湿病学
CiteScore
11.70
自引率
7.10%
发文量
802
审稿时长
52 days
期刊介绍: Osteoarthritis and Cartilage is the official journal of the Osteoarthritis Research Society International. It is an international, multidisciplinary journal that disseminates information for the many kinds of specialists and practitioners concerned with osteoarthritis.
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