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Imaging Mitochondrial Organization in Living Primate Oocytes and Embryos using Multiphoton Microscopy

Published online by Cambridge University Press:  23 May 2003

J.M. Squirrell
Affiliation:
Animal Health and Biomedical Sciences, University of Wisconsin, Madison, WI 53706, USA
R.D. Schramm
Affiliation:
Wisconsin Regional Primate Research Center, University of Wisconsin, Madison, WI 53706, USA
A.M. Paprocki
Affiliation:
Wisconsin Regional Primate Research Center, University of Wisconsin, Madison, WI 53706, USA
D.L. Wokosin
Affiliation:
Laboratory for Optical and Computational Instrumentation, University of Wisconsin, Madison, WI 53706, USA
B.D. Bavister
Affiliation:
Animal Health and Biomedical Sciences, University of Wisconsin, Madison, WI 53706, USA
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Abstract

We employed multiphoton laser scanning microscopy (MPLSM) to image changes in mitochondrial distribution in living rhesus monkey embryos. This method of imaging does not impair development; thus, the same specimen can be visualized multiple times at various developmental stages. Not only does this increase the amount of information that can be gathered on a single specimen but it permits the correlation of early events with subsequent development in the same specimen. Here we demonstrate the utility of MPLSM for determining changes in mitochondrial organization at various developmental stages and show that rhesus zygotes possess a distinct accumulation of mitochondria between the pronuclei prior to syngamy. We present evidence that suggests that this pronuclear accumulation may be positively correlated with development to the blastocyst stage—in the same embryo—thereby illustrating how MPLSM can be used to correlate cellular dynamics of primate oocytes and early embryos with their developmental potential. Understanding the relationship between mitochondrial distribution and the subsequent development of mammalian embryos, particularly primates, will increase our ability to improve embryo culture technologies, including those used for human assisted reproduction.

Type
Research Article
Copyright
2003 Microscopy Society of America

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