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MRI analysis of cerebellar and vestibular developmental phenotypes in Gbx2 conditional knockout mice
Author(s) -
Szulc Kamila U.,
Nieman Brian J.,
Houston Edward J.,
Bartelle Benjamin B.,
Lerch Jason P.,
Joyner Alexandra L.,
Turnbull Daniel H.
Publication year - 2013
Publication title -
magnetic resonance in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.696
H-Index - 225
eISSN - 1522-2594
pISSN - 0740-3194
DOI - 10.1002/mrm.24597
Subject(s) - cerebellum , vestibular system , biology , magnetic resonance imaging , phenotype , anatomy , pathology , fixation (population genetics) , conditional gene knockout , neuroscience , medicine , genetics , radiology , gene
Purpose Our aim in this study was to apply three‐dimensional MRI methods to analyze early postnatal morphological phenotypes in a Gbx2 conditional knockout ( Gbx2‐ CKO ) mouse that has variable midline deletions in the central cerebellum, reminiscent of many human cerebellar hypoplasia syndromes. Methods In vivo three‐dimensional manganese‐enhanced MRI at 100‐µm isotropic resolution was used to visualize mouse brains between postnatal days 3 and 11, when cerebellum morphology undergoes dramatic changes. Deformation‐based morphometry and volumetric analysis of manganese‐enhanced MRI images were used to, respectively, detect and quantify morphological phenotypes in Gbx2 ‐CKO mice. Ex vivo micro‐ MRI was performed after perfusion‐fixation with supplemented gadolinium for higher resolution (50‐µm) analysis. Results In vivo manganese‐enhanced MRI and deformation‐based morphometry correctly identified known cerebellar defects in Gbx2‐ CKO mice, and novel phenotypes were discovered in the deep cerebellar nuclei and the vestibulo‐cerebellum, both validated using histology. Ex vivo micro‐MRI revealed subtle phenotypes in both the vestibulo‐cerebellum and the vestibulo‐cochlear organ, providing an interesting example of complementary phenotypes in a sensory organ and its associated brain region. Conclusion These results show the potential of three‐dimensional MRI for detecting and analyzing developmental defects in mouse models of neurodevelopmental diseases. Magn Reson Med 70:1707–1717, 2013. © 2013 Wiley Periodicals, Inc.