Ren Ping, Yang Chunyan, Lofchy Laren A, Wang Guankui, Chen Fangfang, Simberg Dmitri
Department of Thoracic Surgery, The First Hospital of Jilin University; The Skaggs School of Pharmacy and Pharmaceutical Sciences, Department of Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus; Key Laboratory of Zoonoses Research, Ministry of Education, Jilin University.
The Skaggs School of Pharmacy and Pharmaceutical Sciences, Department of Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus; Department of Cardiology, China-Japan Union Hospital of Jilin University.
J Vis Exp. 2020 Aug 13(162). doi: 10.3791/60847.
Ex vivo perfusion is an important physiological tool to study the function of isolated organs (e.g. liver, kidneys). At the same time, due to the small size of mouse organs, ex vivo perfusion of bone, bladder, skin, prostate, and reproductive organs is challenging or not feasible. Here, we report for the first time an in situ lower body perfusion circuit in mice that includes the above tissues, but bypasses the main clearance organs (kidney, liver, and spleen). The circuit is established by cannulating the abdominal aorta and inferior vena cava above the iliac artery and vein and cauterizing peripheral blood vessels. Perfusion is performed via a peristaltic pump with perfusate flow maintained for up to 2 h. In situ staining with fluorescent lectin and Hoechst solution confirmed that the microvasculature was successfully perfused. This mouse model can be a very useful tool for studying pathological processes as well as mechanisms of drug delivery, migration/metastasis of circulating tumor cells into/from the tumor, and interactions of immune system with perfused organs and tissues.
离体灌注是研究离体器官(如肝脏、肾脏)功能的重要生理学工具。同时,由于小鼠器官体积小,对骨骼、膀胱、皮肤、前列腺和生殖器官进行离体灌注具有挑战性或不可行。在此,我们首次报道了一种小鼠原位下体灌注回路,该回路包括上述组织,但绕过了主要的清除器官(肾脏、肝脏和脾脏)。该回路通过在髂动脉和静脉上方的腹主动脉和下腔静脉插管并烧灼外周血管来建立。通过蠕动泵进行灌注,灌注液流量维持长达2小时。用荧光凝集素和Hoechst溶液进行原位染色证实微血管已成功灌注。该小鼠模型可成为研究病理过程以及药物递送机制、循环肿瘤细胞进出肿瘤的迁移/转移以及免疫系统与灌注器官和组织相互作用的非常有用的工具。