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Click here to see what’s new. We describe a new method for imaging leukocytes in vivo by exciting 199499 endogenous protein fluorescence in the ultraviolet UV spectral region where tryptophan is the major fluorophore.
Two-photon excitation near 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 key alleviates the need to introduce exogenous labels, it is potentially applicable for tracking leukocytes and monitoring inflammatory cellular reactions in humans.
Express 6 7 Express 3 9 Boppart, and Stephen A. Express 4 10 Vinokurov, and Pilhan Kim Opt. Express 22 10 Express 5 3 Lakowicz, Principles of Fluorescence Spectroscopy 3rd ed.
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,ey, Costas Pitsillides, Judith M. Lin, “Imaging leukocyte trafficking in vivo with two-photon-excited endogenous tryptophan fluorescence,” Opt. Express 18 October 21, Revised Manuscript: December 13, Manuscript Accepted: December 21, Published: Abstract Full Article Figures 7 Suppl.
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.
In vivo visualization of skin inflammation by optical coherence tomography and two-photon microscopy Bumju Kim, Seung Lsy Lee, Calvin J. In vivo imaging of immune cell dynamics in skin in response to zinc-oxide nanoparticle exposure Benedikt W.
Optics Express Andrew M.
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