Thurston Arthritis Research Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Department of Medicine, Division of Gastroenterology and Hepatology, and Microbiome Core Facility, Center for Gastrointestinal Biology and Disease, School of Medicine, University of North Carolina, Chapel Hill, NC, USA.
Osteoarthritis Cartilage. 2018 Aug;26(8):1098-1109. doi: 10.1016/j.joca.2018.05.016. Epub 2018 May 30.
To determine the contribution of the gut microbiota to the development of injury-induced osteoarthritis (OA).
OA was induced using the destabilized medial meniscus (DMM) model in 20 germ-free (GF) C57BL/6J male mice housed in a gnotobiotic facility and 23 strain-matched specific pathogen free (SPF) mice in 2 age groups -13.5 weeks avg age at DMM (17 SPF and 15 GF) and 43 weeks avg age at DMM (6 SPF and 5 GF). OA severity was measured using scores for articular cartilage structure (ACS), loss of safranin O (SafO) staining, osteophyte size, and synovial hyperplasia. Microbiome analysis by 16S rRNA amplicon sequencing was performed on stool samples and LPS and LPS binding protein (LBP) were measured in plasma.
Compared to the SPF DMM mice, the maximum (MAX) ACS score per joint was 28% lower (p = 0.036) in GF DMM mice while the SafO sum score of all sections evaluated per joint was decreased by 31% (p = 0.009). The differences between SPF and GF mice in these scores were greater when only the younger mice were included in the analysis. The younger GF DMM mice also had significant reductions in osteophyte size (36%, P = 0.0119) and LBP (27%, P = 0.007) but not synovial scores or LPS. Differences in relative abundance of a number of Operational Taxonomic Units (OTUs) were noted between SPF mice with high vs low maximum ACS scores.
These results suggest factors related to the gut microbiota promote the development of OA after joint injury.
确定肠道微生物群对损伤诱导性骨关节炎(OA)发展的贡献。
在无菌(GF)C57BL/6J 雄性小鼠饲养的无菌设施中,使用不稳定内侧半月板(DMM)模型诱导 OA,共 20 只,以及 23 只同基因无特定病原体(SPF)小鼠,分为 2 个年龄组 - DMM 时平均年龄 13.5 周(17 只 SPF 和 15 只 GF)和 DMM 时平均年龄 43 周(6 只 SPF 和 5 只 GF)。使用关节软骨结构(ACS)评分、番红 O(SafO)染色丢失、骨赘大小和滑膜增生来测量 OA 严重程度。通过 16S rRNA 扩增子测序对粪便样本进行微生物组分析,并测量血浆中的脂多糖(LPS)和 LPS 结合蛋白(LBP)。
与 SPF DMM 小鼠相比,GF DMM 小鼠每关节的最大(MAX)ACS 评分低 28%(p = 0.036),而每关节评估的所有切片的 SafO 总和评分降低 31%(p = 0.009)。当仅分析较年轻的小鼠时,SPF 和 GF 小鼠在这些评分中的差异更大。较年轻的 GF DMM 小鼠的骨赘大小(36%,P = 0.0119)和 LBP(27%,P = 0.007)也有显著降低,但滑膜评分或 LPS 没有降低。在 SPF 小鼠中,具有高 MAX ACS 评分与低 MAX ACS 评分的小鼠之间,注意到一些操作分类单元(OTUs)的相对丰度存在差异。
这些结果表明与肠道微生物群相关的因素促进了关节损伤后 OA 的发展。