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High‐resolution MRI of early‐stage mouse embryos
Author(s) -
Parasoglou Prodromos,
BerriosOtero Cesar A.,
Nieman Brian J.,
Turnbull Daniel H.
Publication year - 2013
Publication title -
nmr in biomedicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.278
H-Index - 114
eISSN - 1099-1492
pISSN - 0952-3480
DOI - 10.1002/nbm.2843
Subject(s) - embryo , organogenesis , biology , phenotype , in utero , magnetic resonance imaging , ex vivo , computational biology , embryogenesis , neuroscience , bioinformatics , in vivo , microbiology and biotechnology , genetics , gene , medicine , fetus , pregnancy , radiology
Both the availability of methods to manipulate genes and the completion of the mouse genome sequence have led to the generation of thousands of genetically modified mouse lines that provide a new platform for the study of mammalian development and developmental diseases. Phenotyping of mouse embryos has traditionally been performed on fixed embryos by the use of ex vivo histological, optical and high‐resolution MRI techniques. Although potentially powerful, longitudinal imaging of individual animals is difficult or impossible with conventional optical methods because of the inaccessibility of mouse embryos inside the maternal uterus. To address this problem, we present a method of imaging the mouse embryo from stages as early as embryonic day (E)10.5, close to the onset of organogenesis in most physiological systems. This method uses a self‐gated MRI protocol, combined with image registration, to obtain whole‐embryo high‐resolution (100 µm isotropic) three‐dimensional images. Using this approach, we demonstrate high contrast in the cerebral vasculature, limbs, spine and central nervous system without the use of contrast agents. These results indicate the potential of MRI for the longitudinal imaging of developing mouse embryos in utero and for future applications in analyzing mutant mouse phenotypes. Copyright © 2012 John Wiley & Sons, Ltd.