Literature DB >> 7803845

Time-lapse total internal reflection fluorescence video of acetylcholine receptor cluster formation on myotubes.

M D Wang1, D Axelrod.   

Abstract

To study when and where acetylcholine receptor (AChR) clusters appear on developing rat myotubes in primary culture, we have made time-lapse movies of total internal reflection fluorescence (TIRF) overlaid with schlieren transmitted light images. The receptors, including the ones newly incorporated into the membrane, were labeled with rhodamine alpha-bungarotoxin (R-BT) continuously present in the medium. Since TIRF illuminates only cell-substrate contact regions where almost all of the AChR clusters are located, background fluorescence from fluorophores either in the bulk solution or inside the cells can be suppressed. Also, because TIRF minimizes the exposure of the cell interior to light, the healthy survival of the culture during imaging procedures is much enhanced relative to standard epi- (or trans-) illumination. During the experiment, cells were kept alive on the microscope stage at 37 degrees C in an atmosphere of 10% CO2. Two digital images were recorded by a CCD camera every 20 min: the schlieren image of the cells and the TIRF image of the clusters. After background subtraction, the cluster image was displayed in pseudocolors, overlaid onto the cell images, and recorded as 3 frames on a videotape. The final movies are thus able to summarize a week-long experiment in less than a minute. These movies and images show that clusters form often shortly after the myoblast fusion but sometimes much later, and the formation takes place very rapidly (a few hours). The clusters have an average lifetime of around a day, much shorter than the lifetime of a typical myotube. The brightest and largest clusters tend to be the longest-lived. The cluster formation seems to be associated with the contacts of myotubes at the glass substrate, but not with cell-cell contacts or myoblast fusion into myotubes. New AChR continuously appear in preexisting clusters: after photobleaching, the fluorescence of some clusters recovers within an hour.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7803845     DOI: 10.1002/aja.1002010104

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  4 in total

1.  A two-compartment microfluidic device for long-term live cell detection based on surface plasmon resonance.

Authors:  Shijie Deng; Xinglong Yu; Ran Liu; Weixing Chen; Peng Wang
Journal:  Biomicrofluidics       Date:  2016-08-03       Impact factor: 2.800

2.  Fluorescently-Labeled Estradiol Internalization and Membrane Trafficking in Live N-38 Neuronal Cells Visualized with Total Internal Reflection Fluorescence Microscopy.

Authors:  Kassandra Kisler; Robert H Chow; Reymundo Dominguez
Journal:  J Steroids Horm Sci       Date:  2013-04-20

Review 3.  Total Internal Reflection Fluorescence (TIRF) Microscopy.

Authors:  Kenneth N Fish
Journal:  Curr Protoc       Date:  2022-08

4.  Improved surface-patterned platinum microelectrodes for the study of exocytotic events.

Authors:  Khajak Berberian; Kassandra Kisler; Qinghua Fang; Manfred Lindau
Journal:  Anal Chem       Date:  2009-11-01       Impact factor: 6.986

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.