Department of Emergency, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Department of Stomatology, The People's Hospital of Longhua, Shenzhen, China.
J Cell Physiol. 2019 Apr;234(4):4668-4680. doi: 10.1002/jcp.27267. Epub 2018 Sep 24.
Arecoline induces oral submucous fibrosis (OSF) via promoting the reactive oxygen species (ROS). Angiotensin (1-7) (Ang-(1-7)) protects against fibrosis by counteracting angiotensin II (Ang-II) via the Mas receptor. However, the effects of Ang-(1-7) on OSF remain unknown. NOD-like receptors (NLRs) family pyrin domain containing 3 (NLRP3) inflammasome is identified as the novel mechanism of fibrosis. Whereas the effects of arecoline on NLRP3 inflammasome remain unclear. We aimed to explore the effect of Ang-(1-7) on NLRP3 inflammasome in human oral myofibroblasts. In vivo, activation of NLRP3 inflammasomes with an increase of Ang-II type 1 receptor (AT1R) protein level and ROS production in human oral fibrosis tissues. Ang-(1-7) improved arecoline-induced rats OSF, reduced protein levels of NADPH oxidase 4 (NOX4) and the NLRP3 inflammasome. In vitro, arecoline increased ROS along with upregulation of the angiotensin-converting enzyme (ACE)/Ang-II/AT1R axis and NLRP3 inflammasome/interleukin-1β axis in human oral myofibroblasts, which were reduced by NOX4 inhibitor VAS2870, ROS scavenger N-acetylcysteine, and NOX4 small interfering RNA (siRNA). Furthermore, arecoline induced collagen synthesis or migration via the Smad or RhoA-ROCK pathway respectively, which could be inhibited by NLRP3 siRNA or caspase-1 blocker VX-765. Ang-(1-7) shifted the balance of RAS toward the ACE2/Ang-(1-7)/Mas axis, inhibited arecoline-induced ROS and NLRP3 inflammasome activation, leading to attenuation of migration or collagen synthesis. In summary, Ang-(1-7) attenuates arecoline-induced migration and collagen synthesis via inhibiting NLRP3 inflammasome in human oral myofibroblasts.
槟榔碱通过促进活性氧(ROS)诱导口腔黏膜下纤维化为(OSF)。血管紧张素(1-7)(Ang-(1-7))通过 Mas 受体拮抗血管紧张素 II(Ang-II)来保护组织免受纤维化。然而,Ang-(1-7)对 OSF 的影响尚不清楚。NOD 样受体(NLRs)家族包含pyrin 结构域的 3(NLRP3)炎性小体被确定为纤维化的新机制。然而,槟榔碱对 NLRP3 炎性小体的影响尚不清楚。我们旨在探讨 Ang-(1-7)对人口腔成纤维细胞中 NLRP3 炎性小体的作用。在体内,在人口腔纤维化组织中,NLRP3 炎性小体的激活伴随着 Ang-II 型 1 受体(AT1R)蛋白水平的增加和 ROS 的产生。Ang-(1-7)改善了槟榔碱诱导的大鼠 OSF,降低了 NADPH 氧化酶 4(NOX4)和 NLRP3 炎性小体的蛋白水平。在体外,槟榔碱增加了 ROS,同时上调了血管紧张素转换酶(ACE)/Ang-II/AT1R 轴和 NLRP3 炎性小体/白细胞介素-1β轴在人口腔成纤维细胞中,这被 NOX4 抑制剂 VAS2870、ROS 清除剂 N-乙酰半胱氨酸和 NOX4 小干扰 RNA(siRNA)降低。此外,槟榔碱通过 Smad 或 RhoA-ROCK 通路分别诱导胶原合成或迁移,这可以被 NLRP3 siRNA 或半胱氨酸蛋白酶-1 阻断剂 VX-765 抑制。Ang-(1-7)将 RAS 的平衡向 ACE2/Ang-(1-7)/Mas 轴倾斜,抑制槟榔碱诱导的 ROS 和 NLRP3 炎性小体激活,从而减弱迁移或胶原合成。总之,Ang-(1-7)通过抑制人口腔成纤维细胞中的 NLRP3 炎性小体来减轻槟榔碱诱导的迁移和胶原合成。