Full developmental potential of mammalian preimplantation embryos is maintained after imaging using a spinning-disk confocal microscope.

Abstract:

:Fluorescent live imaging of cells and embryos at subcellular resolution poses significant challenges for biologists due to morbidity and mortality ensuing from phototoxicity. Here we report the use of a spinning-disk confocal microscope to image mouse and bovine preimplantation embryos without impairing their developmental potential. We also present data indicating that this imaging technique does not affect the functionality of subcellular components as assessed by reactive oxygen species (ROS) production, caspase activity, and DNA integrity. Spinning-disk confocal microscopy was also useful in determining cell number and allocation in transgenic bovine blastocysts. We conclude that this imaging method is suitable for monitoring preimplantation embryos.

journal_name

Biotechniques

journal_title

BioTechniques

authors

Ross PJ,Perez GI,Ko T,Yoo MS,Cibelli JB

doi

10.2144/000112310

subject

Has Abstract

pub_date

2006-12-01 00:00:00

pages

741-50

issue

6

eissn

0736-6205

issn

1940-9818

pii

000112310

journal_volume

41

pub_type

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