Novel light microscopy imaging techniques in nephrology
- 1 July 2003
- journal article
- Published by Wolters Kluwer Health in Current Opinion in Nephrology and Hypertension
- Vol. 12 (4) , 455-461
- https://doi.org/10.1097/00041552-200307000-00015
Abstract
Purpose of review As more genomes are sequenced, the difficult task of characterizing the gene products of these genomes becomes the compelling mission of biological sciences. The melding of whole organ physiology with transgenic animal models, gene transfer methods and RNA silencing promises to form the next wave of scientific inquiry. A host of new microscopy imaging technologies enables researchers to directly visualize gene products, probe alterations in cell function in transgenic animals and map tissue organization. This review will describe these microscopy imaging techniques, their advantages, imaging properties and limitations. Recent findings New optical methods such as two-photon confocal microscopy, fluorescence resonance energy transfer, and total internal fluorescence reflectance microscopy are increasingly being applied to extend our understanding of whole organ and renal epithelial function. Two-photon confocal microscopy has been used to image directly into the kidney of living animals. Fluorescence resonance energy transfer has been used to directly visualize transcription factor complexes within the nucleus while total internal fluorescence reflectance microscopy has permitted direct observation of protein delivery to the plasma membrane. Summary The application of these optical techniques along with the ability to label virtually any protein with a fluorescent tag will enable researchers to study cellular processes and whole organ function in vivo. Light microscopy methods will allow an advance from semi-quantitative to quantitative approaches to problems of relevance to physiologists studying issues related to renal function.Keywords
This publication has 30 references indexed in Scilit:
- Three‐dimensional imaging of human skin and mucosa by two‐photon laser scanning microscopyJournal of Cutaneous Pathology, 2002
- Functional studies of the kidney of living animals using multicolor two-photon microscopyAmerican Journal of Physiology-Cell Physiology, 2002
- Distal ureter morphogenesis depends on epithelial cell remodeling mediated by vitamin A and RetNature Genetics, 2002
- Directionally selective calcium signals in dendrites of starburst amacrine cellsNature, 2002
- Adaptive aberration correction in a confocal microscopeProceedings of the National Academy of Sciences, 2002
- A Miniature Head-Mounted Two-Photon MicroscopeNeuron, 2001
- Odour‐evoked [Ca2+] transients in mitral cell dendrites of frog olfactory glomeruliEuropean Journal of Neuroscience, 2001
- Three-Dimensional Imaging of Embryonic Mouse Kidney by Two-Photon MicroscopyThe American Journal of Pathology, 2001
- Two-Photon Laser Scanning Fluorescence MicroscopyScience, 1990
- Tandem-Scanning Reflected-Light Microscope*Journal of the Optical Society of America, 1968