Acridine orange leukocyte fluorography in mice


Autoria(s): Cahoon, Judd M; Olson, Paul R; Nielson, Spencer; Miya, Tadashi R; Bankhead, Peter; McGeown, J. Graham; Curtis, Timothy M; Ambati, Balamurali K
Data(s)

01/03/2014

Resumo

Simultaneous non-invasive visualization of blood vessels and nerves in patients can be obtained in the eye. The retinal vasculature is a target of many retinopathies. Inflammation, readily manifest by leukocyte adhesion to the endothelial lining, is a key pathophysiological mechanism of many retinopathies, making it a valuable and ubiquitous target for disease research. Leukocyte fluorography has been extensively used in the past twenty years; however, fluorescent markers, visualization techniques, and recording methods have differed between studies. The lack of detailed protocol papers regarding leukocyte fluorography, coupled with lack of uniformity between studies, has led to a paucity of standards for leukocyte transit (velocity, adherence, extravasation) in the retina. Here, we give a detailed description of a convenient method using acridine orange (AO) and a commercially available scanning laser ophthalmoscope (SLO, HRA-OCT Spectralis) to view leukocyte behavior in the mouse retina. Normal mice are compared to mice with acute and chronic inflammation. This method can be readily adopted in many research labs.

Identificador

http://pure.qub.ac.uk/portal/en/publications/acridine-orange-leukocyte-fluorography-in-mice(0977bf59-727d-405f-8bce-29f81fa3ee2a).html

http://dx.doi.org/10.1016/j.exer.2013.12.002

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Cahoon , J M , Olson , P R , Nielson , S , Miya , T R , Bankhead , P , McGeown , J G , Curtis , T M & Ambati , B K 2014 , ' Acridine orange leukocyte fluorography in mice ' Experimental Eye Research , vol 120 , pp. 15-19 . DOI: 10.1016/j.exer.2013.12.002

Palavras-Chave #/dk/atira/pure/subjectarea/asjc/2700/2731 #Ophthalmology #/dk/atira/pure/subjectarea/asjc/2800/2809 #Sensory Systems #/dk/atira/pure/subjectarea/asjc/2800/2804 #Cellular and Molecular Neuroscience
Tipo

article