Please use this identifier to cite or link to this item:
|Title:||Imaging leukocyte trafficking in vivo with two-photon-excited endogenous tryptophan fluorescence||Authors:||Li, Chunqiang
Pastila, Riikka K.
|Keywords:||Leucocytes;Fluorescence;Amino acids;Cells;Mice;Photons||Issue Date:||2010||Publisher:||The Optical Society||Source:||Optics express, 2010, Volume 18, Issue 2, Pages 988-999||Abstract:||We describe a new method for imaging leukocytes in vivo by exciting the endogenous protein fluorescence in the ultraviolet (UV) spectral region where tryptophan is the major fluorophore. Two-photon excitation near 590 nm allows noninvasive optical sectioning through the epidermal cell layers into the dermis of mouse skin, where leukocytes can be observed by video-rate microscopy to interact dynamically with the dermal vascular endothelium. Inflammation significantly enhances leukocyte rolling, adhesion, and tissue infiltration. After exiting the vasculature, leukocytes continue to move actively in tissue as observed by time-lapse microscopy, and are distinguishable from resident autofluorescent cells that are not motile. Because the new method alleviates the need to introduce exogenous labels, it is potentially applicable for tracking leukocytes and monitoring inflammatory cellular reactions in humans||URI:||http://ktisis.cut.ac.cy/handle/10488/7343||ISSN:||1094-4087||DOI:||10.1364/OE.18.000988||Rights:||© 2010 Optical Society of America||Type:||Article|
|Appears in Collections:||Άρθρα/Articles|
Show full item record
checked on Aug 19, 2019
WEB OF SCIENCETM
checked on Aug 14, 2019
checked on Aug 20, 2019
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.