Abbreviated Journal Title
CYCLIC RGD PEPTIDES; TISSUE; ALPHA(V)BETA(3); RECOGNITION; INTEGRINS; Multidisciplinary Sciences
Deep imaging within tissue (over 300 mu m) at micrometer resolution has become possible with the advent of two-photon fluorescence microscopy (2PFM). The advantages of 2PFM have been used to interrogate endogenous and exogenous fluorophores in the skin. Herein, we employed the integrin (cell-adhesion proteins expressed by invading angiogenic blood vessels) targeting characteristics of a two-photon absorbing fluorescent probe to image new vasculature and fibroblasts up to approximate to 1600 mu m within wound (neodermis)/granulation tissue in lesions made on the skin of mice. Reconstruction revealed three dimensional (3D) architecture of the vascular plexus forming at the regenerating wound tissue and the presence of a fibroblast bed surrounding the capillaries. Biologically crucial events, such as angiogenesis for wound healing, may be illustrated and analyzed in 3D on the whole organ level, providing novel tools for biomedical applications.
Yanez, Ciceron O.; Morales, Alma R.; Yue, Xiling; Urakami, Takeo; Komatsu, Masanobu; Jarvinen, Tero A. H.; and Belfield, Kevin D., "Deep Vascular Imaging in Wounds by Two-Photon Fluorescence Microscopy" (2013). Faculty Bibliography 2010s. 4887.