Mesenchymal Stem Cells Reduce Inflammation in a Mouse Model of Lyme Arthritis.

IF 3.3 3区 医学 Q2 CELL & TISSUE ENGINEERING
Stem Cells International Pub Date : 2025-07-28 eCollection Date: 2025-01-01 DOI:10.1155/sci/4363386
Weijiang Ma, Jing Kong, Mengqin Zhang, Hanxin Wu, Shanshan Wan, Xin Liu, Bingxue Li, Yan Dong, Lei Zhong, Weijie Ma, Li Gao, Xinya Wu, Li Peng, Suyi Luo, Zhenhua Ji, Yuxin Fan, Jingjing Chen, Meixiao Liu, Liangyu Zhu, Xun Huang, Rui Yang, Jieqin Song, Fukai Bao, Aihua Liu
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引用次数: 0

Abstract

Lyme disease (LD), a zoonotic infectious disease caused by Borrelia burgdorferi (B. burgdorferi), can affect various organs, including the skin, heart, nervous system, and joints. Lyme arthritis (LA) is the most common and severe late-stage presentation of LD, often presenting with intermittent joint swelling and pain. Although antibiotics are effective in most patients with LA, some patients may continue to experience arthritis symptoms for months or years after standard treatment, which poses a serious threat to their quality of life. Therefore, more effective treatments are urgently needed. The purpose of this study was to evaluate the therapeutic effects of human umbilical cord mesenchymal stem cells (hUC-MSCs) on LD in Kunming (KM) mice. A bilateral hind limb LA model was established by infecting KM mice with B. burgdorferi. Low and high doses of hUC-MSCs (1 × 106 and 2 × 106 cells, respectively) were injected (one time every 2 days) into the right tibiotalar joints of the mice, whereas the left tibiotalar joints were pricked without injecting cells (sham operation). The therapeutic effects of the hUC-MSCs were evaluated through morphological examination, measurement of hind limb diameter, imaging assessment (X-ray), and measurement of inflammatory factor levels. Spirochete burden was assessed by quantitative real-time polymerase chain reaction (qPCR). Morphological, hind limb diameter, and imaging analyses showed that the low and high hUC-MSC doses significantly reduced bilateral hind limb swelling in the LA mice. Histological (hematoxylin and eosin staining) examination of tibiotalar joint sections showed that when compared with the control group, inflammatory cell infiltration, and bilateral hind limb tissue damage were reduced in the two treatment groups. Enzyme-linked immunosorbent assays revealed that the levels of IL-6 and TNF-α in lysates from the bilateral tibiotarsal joints were significantly lower in the two treatment groups than in the control group. QPCR results showed that hUC-MSCs treatment had no significant effect on the spirochete load in the tibiotarsal joint. Our findings indicate that hUC-MSCs can alleviate inflammation in the KM mouse model of LA without increasing B. burgdorferi burden., which is expected to be a new potential method for the treatment of LA.

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间充质干细胞减少莱姆病小鼠模型的炎症。
莱姆病(LD)是一种由伯氏疏螺旋体(伯氏疏螺旋体)引起的人畜共患传染病,可影响各种器官,包括皮肤、心脏、神经系统和关节。莱姆病关节炎(LA)是LD最常见和最严重的晚期表现,通常表现为间歇性关节肿胀和疼痛。虽然抗生素对大多数LA患者有效,但一些患者在标准治疗后可能会持续数月或数年的关节炎症状,这对他们的生活质量构成严重威胁。因此,迫切需要更有效的治疗方法。本研究旨在评价人脐带间充质干细胞(hUC-MSCs)对昆明(KM)小鼠LD的治疗作用。采用伯氏疏螺旋体感染KM小鼠,建立双侧后肢LA模型。将低剂量和高剂量hUC-MSCs(分别为1 × 106和2 × 106细胞)注射到小鼠的右侧胫骨关节(每2天1次),而在左侧胫骨关节穿刺不注射细胞(假手术)。通过形态学检查、后肢直径测量、影像学评估(x线)和炎症因子水平测量来评价hUC-MSCs的治疗效果。采用实时定量聚合酶链反应(qPCR)评估螺旋体负荷。形态学、后肢直径和影像学分析显示,低剂量和高剂量的hUC-MSC显著降低了LA小鼠双侧后肢肿胀。胫骨关节切片组织学(苏木精和伊红染色)检查显示,与对照组相比,两组患者的炎症细胞浸润和双侧后肢组织损伤均减轻。酶联免疫吸附试验显示,两组大鼠双侧胫跖关节裂解物中IL-6和TNF-α水平均显著低于对照组。QPCR结果显示,hUC-MSCs处理对胫跖关节内螺旋体负荷无显著影响。我们的研究结果表明,hUC-MSCs可以减轻LA KM小鼠模型的炎症,而不会增加伯氏疏螺旋体负担。,有望成为治疗LA的一种有潜力的新方法。
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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来源期刊
Stem Cells International
Stem Cells International CELL & TISSUE ENGINEERING-
CiteScore
8.10
自引率
2.30%
发文量
188
审稿时长
18 weeks
期刊介绍: Stem Cells International is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies in all areas of stem cell biology and applications. The journal will consider basic, translational, and clinical research, including animal models and clinical trials. Topics covered include, but are not limited to: embryonic stem cells; induced pluripotent stem cells; tissue-specific stem cells; stem cell differentiation; genetics and epigenetics; cancer stem cells; stem cell technologies; ethical, legal, and social issues.
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