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PMID: 19305125 Published · ppublish English Evaluation Study Journal Article Research Support, Non-U.S. Gov't

Long-term, six-dimensional live-cell imaging for the mouse preimplantation embryo that does not affect full-term development.

The Journal of reproduction and development ·Vol. 55 ·No. 3 ·2009-06-00 ·Pages 343-50

Yamagata K, Suetsugu R, Wakayama T

Abstract

Mammalian preimplantation embryonic development is achieved by tightly coordinated regulation of a great variety of temporal and spatial changes. Therefore, it would be valuable to analyze these events three-dimensionally and dynamically. We have previously developed a live-cell imaging method based on the expression of fluorescent proteins, using mRNA injection and time-lapse florescence microscopy. However, with conventional fluorescent microscopy, three-dimensional images could not be obtained due to the thickness of the embryos and the optical problem in which ;out-of focus blur' cannot be eliminated. Moreover, as the repeated exposure of intense excitation light to the cell yields phototoxicity, long-term observation was detrimental to embryonic development. Here, we improved our imaging system to enable six-dimensional live-cell imaging of mouse preimplantation embryos (x, y and z axes, time-lapse, multicolor and multisample). Importantly, by improving the imaging devices and optimizing the conditions for imaging, such as intensity of excitation and time intervals for image acquisition, the procedure itself was not detrimental to full-term development, although it is a prolonged imaging process. For example, live pups were obtained from embryos to which two different wavelengths of excitation (488 and 561 nm) were applied at 7.5-min intervals for about 70 h, and 51 images were acquired in the z axis at each time point; thus, a total of 56,814 fluorescent images were taken. All the pups were healthy, reproductively normal and not transgenic. Thus, this live-cell imaging technology is safe for full-term mouse development. This offers a novel approach for developmental and reproductive research in that it enables both retrospective and prospective analyses of development. It might also be applicable to assessment of embryo quality in fields such as human reproductive technology and production animal research.

MeSH Terms
Animals Blastocyst/cytology,drug effects,metabolism Cell Survival/physiology Diagnostic Imaging/methods Embryonic Development/physiology Female Gene Transfer Techniques Green Fluorescent Proteins/administration & dosage,genetics,metabolism Male Mice Mice, Inbred C57BL Mice, Inbred DBA Mice, Inbred ICR Mice, Transgenic Microinjections/methods Models, Biological Pregnancy RNA, Messenger/administration & dosage,pharmacology Term Birth Time Factors
Chemicals
RNA, Messenger enhanced green fluorescent protein Green Fluorescent Proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Yamagata Kazuo
Laboratory for Genomic Reprogramming, Center for Developmental Biology, RIKEN-Kobe. [email protected]
Suetsugu Rinako
Wakayama Teruhiko
Article Info
Journal
The Journal of reproduction and development
Abbr.
J Reprod Dev
ISSN
0916-8818
Published
2009-06-00
Epub
2009-00-19
Pages
343-50
Language
English
Region
Japan
NLM ID
9438792
Subset
IM
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