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低强度激光照射通过调节细胞内环腺苷酸水平和 NF-κB 活性抑制人脂肪来源干细胞的炎症反应。

Low-power laser irradiation suppresses inflammatory response of human adipose-derived stem cells by modulating intracellular cyclic AMP level and NF-κB activity.

机构信息

Institute of Biomedical Engineering, National Cheng Kung University, Tainan, Taiwan, Republic of China.

出版信息

PLoS One. 2013;8(1):e54067. doi: 10.1371/journal.pone.0054067. Epub 2013 Jan 16.

Abstract

Mesenchymal stem cell (MSC)-based tissue regeneration is a promising therapeutic strategy for treating damaged tissues. However, the inflammatory microenvironment that exists at a local injury site might restrict reconstruction. Low-power laser irradiation (LPLI) has been widely applied to retard the inflammatory reaction. The purpose of this study was to investigate the anti-inflammatory effect of LPLI on human adipose-derived stem cells (hADSCs) in an inflammatory environment. We showed that the hADSCs expressed Toll-like Receptors (TLR) 1, TLR2, TLR3, TLR4, and TLR6 and that lipopolysaccharide (LPS) significantly induced the production of pro-inflammatory cytokines (Cyclooxygenase-2 (Cox-2), Interleukin-1β (IL-1β), Interleukin-6 (IL-6), and Interleukin-8 (IL-8)). LPLI markedly inhibited LPS-induced, pro-inflammatory cytokine expression at an optimal dose of 8 J/cm². The inhibitory effect triggered by LPLI might occur through an increase in the intracellular level of cyclic AMP (cAMP), which acts to down-regulate nuclear factor kappa B (NF-κB) transcriptional activity. These data collectively provide insight for further investigations of the potential application of anti-inflammatory treatment followed by stem cell therapy.

摘要

基于间充质干细胞(MSC)的组织再生是治疗受损组织的一种很有前途的治疗策略。然而,局部损伤部位存在的炎症微环境可能会限制重建。低强度激光照射(LPLI)已被广泛应用于抑制炎症反应。本研究旨在探讨 LPLI 对炎症环境中脂肪来源间充质干细胞(hADSCs)的抗炎作用。我们发现 hADSCs 表达 Toll 样受体(TLR)1、TLR2、TLR3、TLR4 和 TLR6,脂多糖(LPS)显著诱导促炎细胞因子(环加氧酶-2(Cox-2)、白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)和白细胞介素-8(IL-8))的产生。LPLI 在最佳剂量 8 J/cm² 时显著抑制 LPS 诱导的促炎细胞因子表达。LPLI 触发的抑制作用可能通过增加细胞内环磷酸腺苷(cAMP)的水平而发生,从而下调核因子 kappa B(NF-κB)转录活性。这些数据共同为进一步研究抗炎治疗后干细胞治疗的潜在应用提供了依据。

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