Super-resolution techniques have addressed many biological questions, yet molecular quantification at rapid timescales in live tissues remains challenging. We developed a light microscopy system capable of sub-millisecond sampling to characterize molecular diffusion in heterogeneous aqueous environments comparable to interstitial regions between cells in tissues. We demonstrate our technique wi...

We present a holography-based in vivo optical phase conjugation experiment performed on a living rabbit ear. The motion of live tissues caused the phase conjugate signal to decay with a consistent decay time of less than two seconds. We monitor the signal decay time variation after the ear is excised to postulate different mechanisms that cause the signal decay. The experimental findings addres...

The intrinsic near-infrared photoluminescence (fluorescence) of single-walled carbon nanotubes exhibits unique photostability, narrow bandwidth, penetration through biological media, environmental sensitivity, and both chromatic variety and range. Biomedical applications exploiting this large family of fluorophores will require the spectral and spatial resolution of individual (n,m) nanotube sp...

Mesenchymal stromal cells have shown clinical promise; however, variations in treatment responses are an ongoing concern. We previously demonstrated that MSCs are functionally stunned after thawing. Here, we investigated whether this cryopreservation/thawing defect also impacts the postinfusion biodistribution properties of MSCs. Under both static and physiologic flow, compared with live MSCs i...

Calcification processes are largely unknown in scleractinian corals. In this study, live confocal imaging was used to elucidate the spatiotemporal dynamics of the calcification process in aposymbiotic primary polyps of the coral species Acropora digitifera. The fluorophore calcein was used as a calcium deposition marker and a visible indicator of extracellular fluid distribution at the tissue-s...

The development of new fluorescent probes and green fluorescent protein (GFP) reporter animal models, coupled with improved access to and convenience of imaging technologies, has generated a good deal of excitement in the field of live imaging. One of the challenges that would-be users face is the application of these technologies to live specimens that must remain viable in the imaging setup. ...

The first CT for animal science research was established at our University in 1981. Many years with CT-experiments in live pigs and in carcasses have been carried through over these years. The projects of the 1980s concentrated on testing the accuracies of CT in live pigs (Allen, P. and O. Vangen, several papers 1980s). It was shown that fat was estimated with 97-99 percent accuracy, while prot...

objectives: toxoplasma gondii is a coccidian protozoon which forms tissue cyst in different organs of infected intermediate host. the present study was conducted to demonstrate the active form of parasite in different tissues of rat, which was experimentally infected with rh strain of toxoplasma gondii using bioassay method inmice. materials & methods: in the experimental assay, 75 rats an...

Despite remarkable developments in diffraction unlimited super-resolution microscopy, in vivo nanoscopy of tissues and model organisms is still not satisfactorily established and rarely realized. RESOLFT nanoscopy is particularly suited for live cell imaging because it requires relatively low light levels to overcome the diffraction barrier. Previously, we introduced the reversibly switchable f...

Cells change extensively in their locations and property during embryogenesis. These changes are regulated by the interactions between the cells and their environment. Chimeric embryos, which are composed of cells of different genetic background, are great tools to study the cell-cell interactions mediated by genes of interest. The embryonic transparency of zebrafish at early developmental stag...