Literature DB >> 18754997

Motion-enhanced, differential interference contrast (MEDIC) microscopy of moving vesicles in live cells: VE-DIC updated.

D B Hill1, J C Macosko, G M Holzwarth.   

Abstract

Video-enhanced differential interference contrast microscopy with background subtraction has made visible many structures and processes in living cells. In video-enhanced differential interference contrast, the background image is stored manually by defocusing the microscope before images are acquired. We have updated and improved video-enhanced differential interference contrast by adding automatic generation of the background image as a rolling average of the incoming image stream. Subtraction of this continuously updated 12-bit background image from the incoming 12-bit image stream provides a flat background which allows the contrast of moving objects, such as vesicles, to be strongly enhanced while suppressing stationary features such as the overall cell shape. We call our method MEDIC, for motion-enhanced differential interference contrast. By carrying out background subtraction with 12-bit images, the number of grey levels in the moving vesicles can be maximized and a single look-up table can be applied to the entire image, enhancing the contrast of all vesicles simultaneously. Contrast is increased by as much as a factor of 13. The method is illustrated with raw, background and motion-enhanced differential interference contrast images of moving vesicles within a neurite of a live PC12 cell and a live chick motorneuron.

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Year:  2008        PMID: 18754997      PMCID: PMC2753545          DOI: 10.1111/j.1365-2818.2008.02054.x

Source DB:  PubMed          Journal:  J Microsc        ISSN: 0022-2720            Impact factor:   1.758


  6 in total

1.  Fast vesicle transport in PC12 neurites: velocities and forces.

Authors:  D B Hill; M J Plaza; K Bonin; G Holzwarth
Journal:  Eur Biophys J       Date:  2004-04-08       Impact factor: 1.733

2.  Speckled microtubules improve tracking in motor-protein gliding assays.

Authors:  Ernest N Chisena; R Andrew Wall; Jed C Macosko; George Holzwarth
Journal:  Phys Biol       Date:  2007-02-08       Impact factor: 2.583

3.  Fewer active motors per vesicle may explain slowed vesicle transport in chick motoneurons after three days in vitro.

Authors:  Jed C Macosko; Jason M Newbern; Jean Rockford; Ernest N Chisena; Charlotte M Brown; George M Holzwarth; Carol E Milligan
Journal:  Brain Res       Date:  2008-03-20       Impact factor: 3.252

4.  Video-enhanced microscopy with a computer frame memory.

Authors:  R D Allen; N S Allen
Journal:  J Microsc       Date:  1983-01       Impact factor: 1.758

5.  Video-enhanced contrast, differential interference contrast (AVEC-DIC) microscopy: a new method capable of analyzing microtubule-related motility in the reticulopodial network of Allogromia laticollaris.

Authors:  R D Allen; N S Allen; J L Travis
Journal:  Cell Motil       Date:  1981

6.  Video image processing greatly enhances contrast, quality, and speed in polarization-based microscopy.

Authors:  S Inoué
Journal:  J Cell Biol       Date:  1981-05       Impact factor: 10.539

  6 in total
  2 in total

1.  Intraneuronal vesicular organelle transport changes with cell population density in vitro.

Authors:  Clayton T Bauer; Yuri Shtridelman; Carla M Lema Tomé; Joel Q Grim; Christopher P Turner; Michael Tytell; Jed C Macosko
Journal:  Neurosci Lett       Date:  2008-06-13       Impact factor: 3.046

2.  Force-velocity curves of motor proteins cooperating in vivo.

Authors:  Yuri Shtridelman; Thomas Cahyuti; Brigitte Townsend; David DeWitt; Jed C Macosko
Journal:  Cell Biochem Biophys       Date:  2008       Impact factor: 2.194

  2 in total

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