Three-Dimensional in vivo Reflectance and Fluorescence Imaging by a Handheld Dual-Axes Confocal Microscope

2007 ◽  
Author(s):  
H. Ra ◽  
W. Piyawattanametha ◽  
M. J. Mandella ◽  
J. T. C. Liu ◽  
L. K. Wong ◽  
...  
Keyword(s):  
Fluorescence Imaging ◽  
Three Dimensional ◽  
Confocal Microscope

Three-dimensional imaging of the living eye

1991 ◽  
Vol 49 ◽  
pp. 170-171 ◽  
Author(s):  
Barry R. Masters
Keyword(s):  
Laser Scanning ◽  
Water Immersion ◽  
Physiological State ◽  
Three Dimensional ◽  
Confocal Microscope ◽  
Image Stack ◽  
Rabbit Eye ◽  
Reflected Light

The structure of the in situ rabbit cornea can be observed at high resolution and contrast with reflected light confocal microscopy. In vivo confocal images of the living cornea have been made at lower resolution and lower contrast using a SIT video camera together with a real-time Nipkow disk confocal microscope adapted for in vivo observations. This paper describes the three dimensional reconstruction of the in situ cornea from an enucleated rabbit eye with confocal reflected light microscopy and volume rendering computer techniques.A laser scanning confocal microscope (BioRad MRC 600) was used in the reflected light mode to obtain the two-dimensional image stack from the cornea of a freshly enucleated rabbit eye. The eye was maintained in a physiological state with aerated Ringer's solution. The light source was an argon ion laser with a 488 nm wavelength. The microscope objective was a Leitz X25, NA 0.6 water immersion lens. The 400 micron thick cornea was optically sectioned into 133, three micron sections. The optical sectioning was performed perpendicular to the optical axis of the eye globe.

scholarly journals Three-dimensional in vivo imaging by a handheld dual-axes confocal microscope

2008 ◽  
Vol 16 (10) ◽  
pp. 7224 ◽  
Author(s):  
Hyejun Ra ◽  
Wibool Piyawattanametha ◽  
Michael J. Mandella ◽  
Pei-Lin Hsiung ◽  
Jonathan Hardy ◽  
...  
Keyword(s):  
In Vivo Imaging ◽  
Three Dimensional ◽  
Confocal Microscope

Photoinhibitory printing on leaves, visualised by chlorophyll fluorescence imaging and confocal microscopy, is due to diminished fluorescence from grana

1999 ◽  
Vol 26 (7) ◽  
pp. 717 ◽  
Author(s):  
Barry Osmond ◽  
Owen Schwartz ◽  
Brian Gunning
Keyword(s):  
Chlorophyll Fluorescence ◽  
Fluorescence Imaging ◽  
Imaging System ◽  
Confocal Microscope ◽  
Chlorophyll Fluorescence Imaging ◽  
Grid Pattern ◽  
Chlorophyll Autofluorescence ◽  
The Stability ◽  
Living Tissues

By analogy with the starch printing technique, it was hypothesised that photoinhibition could be used to print images on leaves that would be invisible to the eye, but easily revealed by chlorophyll fluorescence imaging. We first illustrate the process of chlorophyll fluorescence printing on leaves of the shade plant, Cissus rhombifolia, using photographs of artefacts from starch printing experiments in the laboratory of Molisch. We then use portraits of current leaders in chlorophyll fluorescence research to demonstrate the stability of these images in living tissues. Text printing from microfilm of Ewart’s pioneering studies in photoinhibition shows the resolution of the method with the fixed-focus, portable, imaging system used here. The stability of images, as well as quenching analysis of images and of leaves, suggests that localised photoinactivation, rather than sustained photoprotection, is responsible for the detail displayed by fluorescence printing. Electron micrograph positives of stained thylakoids can be printed to create an illusion of what is imagined to be the source of chlorophyll fluorescence at the membrane level. Individual chloroplasts in adjacent cells under the grid pattern of granal stacks printed on leaves were also examined using a confocal microscope. Compared with chloroplasts in the shaded parts of the grid, those in the photoinactivated parts of the grid show greatly reduced chlorophyll autofluorescence. Moreover, these chloroplasts have lost the localised bright fluorescence from grana. Comparisons of fluorescence yields show that relative chlorophyll autofluorescence from grana observed in the confocal microscope parallels that determined in leaves. Our experiments provide direct visual evidence that fluorescence from grana is lost following photoinactivation of photosystem II in vivo.

Development of in vivo confocal microscope for reflection and fluorescence imaging simultaneously

2010 ◽  
Author(s):  
MyoungKi Ahn ◽  
ByungSeon Chun ◽  
Cheol Song ◽  
DaeGab Gweon
Keyword(s):  
Fluorescence Imaging ◽  
Confocal Microscope

In vitro and in vivo polysaccharides assembly: ultrastructural and cytochemical study of growing plant cell wall components.

1978 ◽  
Vol 36 (2) ◽  
pp. 434-435
Author(s):  
D. Reis ◽  
B. Vian ◽  
J. C. Roland
Keyword(s):  
Cell Wall ◽  
Self Assembly ◽  
Plant Cell Wall ◽  
Higher Plants ◽  
Three Dimensional ◽  
Cytochemical Study ◽  
Wall Components

Wall morphogenesis in higher plants is a problem still open to controversy. Until now the possibility of a transmembrane control and the involvement of microtubules were mostly envisaged. Self-assembly processes have been observed in the case of walls of Chlamydomonas and bacteria. Spontaneous gelling interactions between xanthan and galactomannan from Ceratonia have been analyzed very recently. The present work provides indications that some processes of spontaneous aggregation could occur in higher plants during the formation and expansion of cell wall.Observations were performed on hypocotyl of mung bean (Phaseolus aureus) for which growth characteristics and wall composition have been previously defined.In situ, the walls of actively growing cells (primary walls) show an ordered three-dimensional organization (fig. 1). The wall is typically polylamellate with multifibrillar layers alternately transverse and longitudinal. Between these layers intermediate strata exist in which the orientation of microfibrils progressively rotates. Thus a progressive change in the morphogenetic activity occurs.

Three-Dimensional Subcellular Organization of Hepatocytes in Intact Liver: Simultaneous Visualization of Cytoskeletal and Membrane Markers by Confocal Microscopy

1996 ◽  
Vol 54 ◽  
pp. 288-289
Author(s):  
Greg V. Martin ◽  
Ann L. Hubbard
Keyword(s):  
Three Dimensional ◽  
Integral Membrane Proteins ◽  
Polarized Secretion ◽  
Microscope Images ◽  
Computer Aided ◽  
Intracellular Organelles ◽  
Cytoskeletal Elements ◽  
Simultaneous Visualization

The microtubule (MT) cytoskeleton is necessary for many of the polarized functions of hepatocytes. Among the functions dependent on the MT-based cytoskeleton are polarized secretion of proteins, delivery of endocytosed material to lysosomes, and transcytosis of integral plasma membrane (PM) proteins. Although microtubules have been shown to be crucial to the establishment and maintenance of functional and structural polarization in the hepatocyte, little is known about the architecture of the hepatocyte MT cytoskeleton in vivo, particularly with regard to its relationship to PM domains and membranous organelles. Using an in situ extraction technique that preserves both microtubules and cellular membranes, we have developed a protocol for immunofluorescent co-localization of cytoskeletal elements and integral membrane proteins within 20 µm cryosections of fixed rat liver. Computer-aided 3D reconstruction of multi-spectral confocal microscope images was used to visualize the spatial relationships among the MT cytoskeleton, PM domains and intracellular organelles.

The influence of confocal microscope design on imaging performance

1993 ◽  
Vol 51 ◽  
pp. 144-145
Author(s):  
C J R Sheppard
Keyword(s):  
Image Quality ◽  
Fluorescence Imaging ◽  
Confocal Microscope ◽  
Industrial Applications ◽  
Three Dimensions ◽  
Design Parameters ◽  
Weak Signals ◽  
Size And Shape ◽  
Imaging Performance ◽  
Fundamental Limitation

The confocal microscope is now widely used in both biomedical and industrial applications for imaging, in three dimensions, objects with appreciable depth. There are now a range of different microscopes on the market, which have adopted a variety of different designs. The aim of this paper is to explore the effects on imaging performance of design parameters including the method of scanning, the type of detector, and the size and shape of the confocal aperture.It is becoming apparent that there is no such thing as an ideal confocal microscope: all systems have limitations and the best compromise depends on what the microscope is used for and how it is used. The most important compromise at present is between image quality and speed of scanning, which is particularly apparent when imaging with very weak signals. If great speed is not of importance, then the fundamental limitation for fluorescence imaging is the detection of sufficient numbers of photons before the fluorochrome bleaches.

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