Gao Qiongqiong, Gao Zhentao, Su Minzhi, Huang Yong, Zhang Chi, Li Cuiping, Zhan Hailun, Liu Bolong, Zhou Xiangfu
Department of Urology, The Third Affiliated Hospital and Lingnan Hospital of the Sun Yat-Sen University, 2693 Kaichuang Road, Guangzhou 510700, China.
Department of Rehabilitation, The Third Affiliated Hospital and Lingnan Hospital of the Sun Yat-Sen University, 2693 Kaichuang Road, Guangzhou 510700, China.
Stem Cells Int. 2023 Nov 14;2023:8887091. doi: 10.1155/2023/8887091. eCollection 2023.
Interstitial cystitis/bladder pain syndrome (IC/BPS) seriously reduces the patient's quality of life, yet current therapies only provide partial relief. In the spinal dorsal horn (SDH), neuroinflammation plays a pivotal role in the development of IC. Injection of human umbilical cord mesenchymal stem cells (hUMSCs) to reduce inflammation is an effective strategy, and heme oxygenase-1 (HO-1) exhibits anti-nociceptive effect in neuroinflammatory pain. This study aimed to test the therapeutic effects of hUMSCs overexpressing HO-1 on cyclophosphamide-induced cystitis rat model. Cystitis rats were transplanted with altered cells and then assessed for 3 weeks. A series of behavioral measurements would be trial including suprapubic mechanical allodynia, depressive-like behaviors, micturition frequency, and short-term memory function. Additionally, western blot, immunofluorescence staining, and ELISA kit test for anti-inflammation effect. HUMSCs were capable of being transduced to overexpress HO-1. Injection of hUMSCs overexpressing HO-1 was more effective than hUMSCs alone in alleviating behavioral symptoms in rats. Furthermore, hUMSCs overexpressing HO-1 inhibited the activation of glial and TLR4/p65/NLRP3 pathway, decreased the levels of pro-inflammatory cytokines in the SDH region. Surprisingly, it markedly increased anti-inflammatory cytokine IL-10, reduced MDA content, and protected GSH concentrations in local environment. Our results suggest that injecting hUMSCs overexpressing HO-1 intrathecally can significantly promote functional outcomes in cystitis rats by reducing neuroinflammation, at least, partly through downregulating TLR4/p65/NLRP3 signaling pathway in the SDH region. This cell therapy affords a new strategy for IC/BPS treatment.
间质性膀胱炎/膀胱疼痛综合征(IC/BPS)严重降低患者生活质量,但目前的治疗方法只能提供部分缓解。在脊髓背角(SDH)中,神经炎症在IC的发生发展中起关键作用。注射人脐带间充质干细胞(hUMSCs)以减轻炎症是一种有效的策略,血红素加氧酶-1(HO-1)在神经炎性疼痛中具有抗伤害感受作用。本研究旨在测试过表达HO-1的hUMSCs对环磷酰胺诱导的膀胱炎大鼠模型的治疗效果。将改变的细胞移植到膀胱炎大鼠体内,然后进行3周的评估。一系列行为测量将包括耻骨上机械性异常性疼痛、抑郁样行为、排尿频率和短期记忆功能。此外,通过蛋白质免疫印迹法、免疫荧光染色和酶联免疫吸附测定试剂盒检测抗炎效果。hUMSCs能够被转导以过表达HO-1。注射过表达HO-1的hUMSCs在减轻大鼠行为症状方面比单独注射hUMSCs更有效。此外,过表达HO-1的hUMSCs抑制胶质细胞和TLR4/p65/NLRP3通路的激活,降低SDH区域促炎细胞因子的水平。令人惊讶的是,它显著增加抗炎细胞因子IL-10,降低丙二醛含量,并保护局部环境中的谷胱甘肽浓度。我们的结果表明,鞘内注射过表达HO-1的hUMSCs可通过减轻神经炎症,至少部分通过下调SDH区域的TLR4/p65/NLRP3信号通路,显著促进膀胱炎大鼠的功能恢复。这种细胞疗法为IC/BPS的治疗提供了一种新策略。