| Literature DB >> 28060277 |
Chi Ching Goh1, Jackson LiangYao Li2, David Becker3, Wolfgang Weninger4, Veronique Angeli5, Lai Guan Ng6.
Abstract
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).Entities:
Mesh:
Year: 2016 PMID: 28060277 PMCID: PMC5226449 DOI: 10.3791/54956
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355