Lin Cheng-Han, Chen Yi-Ju, Lin Meng-Wei, Chang Ho-Ju, Yang Xin-Rui, Lin Chih-Sheng
Department of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
Center for Intelligent Drug Systems and Smart Bio-Devices (IDS2B), National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
Medicina (Kaunas). 2023 Aug 26;59(9):1554. doi: 10.3390/medicina59091554.
COVID-19 is a highly transmittable respiratory illness caused by SARS-CoV-2, and acute lung injury (ALI) is the major complication of COVID-19. The challenge in studying SARS-CoV-2 pathogenicity is the limited availability of animal models. Therefore, it is necessary to establish animal models that can reproduce multiple characteristics of ALI to study therapeutic applications. The present study established a mouse model that has features of ALI that are similar to COVID-19 syndrome to investigate the role of ACE2 and the administration of the Chinese herbal prescription NRICM101 in ALI. Mice with genetic modifications, including overexpression of human ACE2 (K18-hACE2 TG) and absence of ACE2 (mACE2 KO), were intratracheally instillated with hydrochloric acid. The acid intratracheal instillation induced severe immune cell infiltration, cytokine storms, and pulmonary disease in mice. Compared with K18-hACE2 TG mice, mACE2 KO mice exhibited dramatically increased levels of multiple inflammatory cytokines (IL-6 and TNF-α) in bronchoalveolar lavage fluid, histological evidence of lung injury, and dysregulation of MAPK and MMP activation. In mACE2 KO mice, NRICM101 could ameliorate the disease progression of acid-induced ALI. In conclusion, the established mouse model provided an effective platform for researchers to investigate pathological mechanisms and develop therapeutic strategies for ALI, including COVID-19-related ALI.
新型冠状病毒肺炎(COVID-19)是由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的一种高度传染性的呼吸道疾病,急性肺损伤(ALI)是COVID-19的主要并发症。研究SARS-CoV-2致病性面临的挑战是动物模型的可用性有限。因此,有必要建立能够重现ALI多种特征的动物模型来研究治疗应用。本研究建立了一种具有与COVID-19综合征相似的ALI特征的小鼠模型,以研究血管紧张素转换酶2(ACE2)的作用以及中药复方NRICM101在ALI中的应用。对经过基因改造的小鼠,包括人ACE2过表达(K18-hACE2转基因小鼠)和ACE2缺失(mACE2基因敲除小鼠),进行气管内滴注盐酸。气管内滴注盐酸可诱导小鼠出现严重的免疫细胞浸润、细胞因子风暴和肺部疾病。与K18-hACE2转基因小鼠相比,mACE2基因敲除小鼠支气管肺泡灌洗液中多种炎性细胞因子(白细胞介素-6和肿瘤坏死因子-α)水平显著升高,有肺损伤的组织学证据,且丝裂原活化蛋白激酶(MAPK)和基质金属蛋白酶(MMP)激活失调。在mACE2基因敲除小鼠中,NRICM101可改善酸诱导的ALI的疾病进展。总之,所建立小鼠模型为研究人员研究ALI(包括与COVID-19相关的ALI)的病理机制和制定治疗策略提供了一个有效的平台。