Yin Kan, Zhu Rongjia, Wang Shihua, Zhao Robert Chunhua
Centre of Excellence in Tissue Engineering, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
PLoS One. 2017 Jun 8;12(6):e0179175. doi: 10.1371/journal.pone.0179175. eCollection 2017.
Considering promising results in animal models and patients, therapeutic use of MSCs for immune disease is likely to undergo continued evaluation. Low-lever laser (LLL) has been widely applied to retard the inflammatory reaction. LLL treatment can potentially be applied in anti-inflammatory therapy followed by stem cell therapy.
The purpose of this study was to investigate the effect of LLL (660 nm) on the inflammatory reaction induced by LPS in human adipose derived mesenchymal stem cells (hADSCs) and pertinent mechanism.
Anti-inflammatory activity of LLL was investigated by LPS-induced mesenchymal stem cells. The production and expression of pro-inflammatory cytokines were evaluated by ELISA kits and RT-qPCR. Nuclear translocation of NF-κB was indicated by immunofluorescent staining. Phosphorylation status of NF-κB p65 and IκBα were illustrated by western blot assay. ROS generation was measured with CM-H2DCFDA, and NO secretion was determined by DAF-FM. We studied surface expression of lymphocyte activation markers when Purified peripheral blood mononuclear cell (PBMC) were activated by phytohaemagglutinin (PHA) in the presence of 3 types of treated MSCs.
LLL reduced the secretion of IL-1β, IL-6, IL8, ROS and NO in LPS treated MSCs. Immunofluorescent assay demonstrated the nuclear translocation decrease of NF-κB in LLL treated LPS induced MSCs. Western blot analysis also suggested that LLL suppressed NF-κB activation via regulating the phosphorylation of p65 and IκBα. MSC significantly reduced the expression of activation markers CD25 and CD69 on PHA-stimulated lymphocytes.
The results indicate that LLL suppressed the activation of NF-κB signaling pathway in LPS treated MSCs through inhibiting phosphorylation of p65 and IκBα, which results in good anti-inflammatory effect. In addition, LLL attenuated activation-associated markers CD25 and CD69 in co-cultures of PBMC and 3 types of treated MSCs.
鉴于在动物模型和患者中取得的有前景的结果,间充质干细胞(MSCs)在免疫疾病治疗中的应用可能会持续得到评估。低强度激光(LLL)已被广泛应用于抑制炎症反应。LLL治疗有可能应用于抗炎治疗,随后进行干细胞治疗。
本研究旨在探讨LLL(660nm)对脂多糖(LPS)诱导的人脂肪来源间充质干细胞(hADSCs)炎症反应的影响及相关机制。
通过LPS诱导的间充质干细胞研究LLL的抗炎活性。采用酶联免疫吸附测定试剂盒(ELISA kits)和逆转录定量聚合酶链反应(RT-qPCR)评估促炎细胞因子(pro-inflammatory cytokines)的产生和表达。通过免疫荧光染色显示核因子κB(NF-κB)的核转位。通过蛋白质免疫印迹法(western blot assay)说明NF-κB p65和IκBα的磷酸化状态。用CM-H2DCFDA测量活性氧(ROS)的产生,用DAF-FM测定一氧化氮(NO)的分泌。当纯化的外周血单个核细胞(PBMC)在3种经处理的MSCs存在的情况下被植物血凝素(PHA)激活时,我们研究了淋巴细胞活化标志物的表面表达。
LLL减少了LPS处理的MSCs中白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、白细胞介素-8(IL-8)、ROS和NO的分泌。免疫荧光分析表明,在LLL处理的LPS诱导的MSCs中,NF-κB的核转位减少。蛋白质免疫印迹分析还表明,LLL通过调节p65和IκBα的磷酸化来抑制NF-κB的激活。MSCs显著降低了PHA刺激的淋巴细胞上活化标志物CD25和CD69的表达。
结果表明,LLL通过抑制p65和IκBα的磷酸化来抑制LPS处理的MSCs中NF-κB信号通路的激活,从而产生良好的抗炎效果。此外,LLL减弱了PBMC与3种经处理的MSCs共培养中活化相关标志物CD25和CD69的表达。