Goh Chi Ching, Li Jackson LiangYao, Becker David, Weninger Wolfgang, Angeli Veronique, Ng Lai Guan
Singapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), Biopolis; Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore.
Singapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), Biopolis.
J Vis Exp. 2016 Dec 22(118):54956. doi: 10.3791/54956.
Ischemia-reperfusion injury (IRI) occurs when there is transient hypoxia due to the obstruction of blood flow (ischemia) followed by a subsequent re-oxygenation of the tissues (reperfusion). In the skin, ischemia-reperfusion (IR) is the main contributing factor to the pathophysiology of pressure ulcers. While the cascade of events leading up to the inflammatory response has been well studied, the spatial and temporal responses of the different subsets of immune cells to an IR injury are not well understood. Existing models of IR using the clamping technique on the skin flank are highly invasive and unsuitable for studying immune responses to injury, while similar non-invasive magnet clamping studies in the skin flank are less-than-ideal for intravital imaging studies. In this protocol, we describe a robust model of non-invasive IR developed on mouse ear skin, where we aim to visualize in real-time the cellular response of immune cells after reperfusion via multiphoton intravital imaging (MP-IVM).
缺血再灌注损伤(IRI)发生于因血流阻塞导致短暂性缺氧(缺血),随后组织再充氧(再灌注)之时。在皮肤中,缺血再灌注(IR)是压疮病理生理学的主要促成因素。虽然导致炎症反应的一系列事件已得到充分研究,但不同免疫细胞亚群对IR损伤的时空反应尚不清楚。现有的在侧腹皮肤使用夹闭技术的IR模型具有高度侵入性,不适合研究对损伤的免疫反应,而在侧腹皮肤进行的类似非侵入性磁夹闭研究对于活体成像研究而言并不理想。在本方案中,我们描述了一种在小鼠耳部皮肤建立的非侵入性IR稳健模型,我们旨在通过多光子活体成像(MP-IVM)实时可视化再灌注后免疫细胞的细胞反应。