Differential Interference Contrast (DIC)
To minimize the effects of photobleaching, fluorescence microscopy can be combined with other techniques that are non-destructive to the fluorochrome, such as differential interference contrast (DIC), Hoffman modulation contrast (HMC), transmitted darkfield illumination, and phase contrast.
The idea is to locate a specific area of interest in a specimen using the non-destructive contrast enhancing technique then, without relocating the specimen, switch the microscope to fluorescence mode. The results of a typical experiment of this type are illustrated in Figure 1. Figure 1(a) illustrates a rat retina optic ganglion tissue thin section imaged using differential interference contrast. The photomicrograph in Figure 1(b) shows the same viewfield, but this time imaged using fluorescence illumination (a mercury vapor lamp and an Olympus WU filter cube) with cells stained by the fluorochrome fast blue, a diazonium salt that specifically stains phospholipids in the myelin sheath. Figure 1(c) illustrates the two techniques used in combination to produce a beautiful photomicrograph of fluorescent-stained optic ganglion lipid tissue superimposed on a differential interference contrast image of the retina. This image was recorded with a specialized fluorite objective designed to permit simultaneous observation of both fluorescence and differential interference contrast with the same objective.
The microscope configuration typically utilized to simultaneously image specimens using both differential interference contrast (DIC) and fluorescence illumination is illustrated in Figure 2. DIC is conducted using transmitted light provided by a tungsten-halogen lamp positioned in a lamphouse attached to the microscope base. Light passing through the field diaphragm is reflected by a mirror into the substage condenser and through a Wollaston prism located at the front focal plane of the condenser.
Light diffracted by the specimen is first passed through a second Wollaston prism positioned near the objective rear focal plane before interfering at the intermediate image plane with light passing through the specimen undiffracted. Simultaneously, ultraviolet light emitted by a mercury burner is passed through an exciter filter, then reflected by a dichroic mirror onto the specimen from above. Secondary fluorescence emitted by the chromophore attached to the stained specimen is captured by the objective and passed through the barrier filter and into the eyepieces and/or phototube. This configuration can be used to image specimens using the techniques (fluorescence and differential interference contrast) individually or in combination.
Mortimer Abramowitz - Olympus America, Inc., Two Corporate Center Drive., Melville, New York, 11747.
Michael W. Davidson - National High Magnetic Field Laboratory, 1800 East Paul Dirac Dr., The Florida State University, Tallahassee, Florida, 32310.
BACK TO FLUORESCENCE MICROSCOPY
Questions or comments? Send us an email.
© 1998-2019 by
Michael W. Davidson and The Florida State University.
All Rights Reserved. No images, graphics, scripts, or applets may be reproduced or used in any manner without permission from the copyright holders. Use of this website means you agree to all of the Legal Terms and Conditions set forth by the owners.
Last modification: Tuesday, Sep 11, 2018 at 09:57 AM
Access Count Since July 30, 1998: 64750
For more information on microscope manufacturers,
use the buttons below to navigate to their websites: