An Lemei, Chu Tianshu, Wang Liujun, An Songtao, Li Yalong, Hao Hongbo, Zhang Zhuoli, Yue Han
Department of Rheumatology and Clinical Immunology, Henan Provincial People's Hospital, People's Hospital of Zhengzhou University, Zhengzhou, Henan 450003, P.R. China.
Department of Cardiology, Henan Provincial People's Hospital, People's Hospital of Zhengzhou University, Zhengzhou, Henan 450003, P.R. China.
Exp Ther Med. 2021 Nov;22(5):1272. doi: 10.3892/etm.2021.10707. Epub 2021 Sep 7.
A single injection of low-dose human umbilical cord-derived mesenchymal stem cells (UC-MSCs) has been previously demonstrated to relieve synovitis and bone erosion in animal models of arthritis, but whether frequent injections of high-dose UC-MSCs relieve arthritis and inhibit loss of muscle mass has remained elusive. In the present study, DBA/1 mice were randomly divided into three groups: Normal (wild-type mice; n=11), collagen-induced arthritis (CIA; n=12) and CIA treated with UC-MSCs (n=11; 5x10 UC-MSCs per week for 3 weeks). Arthritis and skeletal muscle cachexia were evaluated until the end of the experiment on day 84. It was indicated that both the CIA and UC-MSC groups had lower body weights compared with the normal mice. Clinical arthritis scores, hind ankle diameters, synovitis and bone erosion progressively increased and were similar between the CIA and UC-MSC groups. Although there was no difference in food intake among the three groups, the normalized food intake of normal group was significantly higher than CIA group and UC-MSC group from day 42 onwards; there was no significance on day 77 but this could be neglected. Furthermore, gastrocnemius muscle weight in the UC-MSC group was significantly reduced compared with that in the CIA and normal groups. The UC-MSC group had higher levels of proinflammatory cytokines, such as TNF-α, IL-6 and IL-1β than those in the CIA group. However, the other cytokines assessed and the fibrosis indices in the CIA and UC-MSC groups were not different from those in the control group and there was no inflammatory cell infiltration. Thus, frequent injections of high-dose UC-MSCs slightly aggravated synovitis and muscle cachexia in the murine CIA model and should therefore be avoided in the treatment of arthritis.
先前已证明,单次注射低剂量人脐带间充质干细胞(UC-MSCs)可缓解关节炎动物模型中的滑膜炎和骨侵蚀,但频繁注射高剂量UC-MSCs是否能缓解关节炎并抑制肌肉量的减少仍不清楚。在本研究中,DBA/1小鼠被随机分为三组:正常组(野生型小鼠;n = 11)、胶原诱导性关节炎组(CIA;n = 12)和接受UC-MSCs治疗的CIA组(n = 11;每周注射5×10个UC-MSCs,共3周)。在实验第84天结束前评估关节炎和骨骼肌恶病质情况。结果表明,与正常小鼠相比,CIA组和UC-MSC组的体重均较低。临床关节炎评分、后踝直径、滑膜炎和骨侵蚀逐渐增加,且CIA组和UC-MSC组相似。虽然三组之间的食物摄入量没有差异,但从第42天起,正常组的标准化食物摄入量显著高于CIA组和UC-MSC组;第77天无显著差异,但可忽略不计。此外,与CIA组和正常组相比,UC-MSC组的腓肠肌重量显著降低。UC-MSC组的促炎细胞因子如TNF-α、IL-6和IL-1β水平高于CIA组。然而,CIA组和UC-MSC组中评估的其他细胞因子以及纤维化指标与对照组无异,且无炎性细胞浸润。因此,在小鼠CIA模型中,频繁注射高剂量UC-MSCs会轻微加重滑膜炎和肌肉恶病质,所以在关节炎治疗中应避免使用。