MRI analysis of cerebellar and vestibular developmental phenotypes in Gbx2 conditional knockout mice

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. Metho...

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Veröffentlicht in:Magnetic resonance in medicine 2013-12, Vol.70 (6), p.1707-1717
Hauptverfasser: Szulc, Kamila U., Nieman, Brian J., Houston, Edward J., Bartelle, Benjamin B., Lerch, Jason P., Joyner, Alexandra L., Turnbull, Daniel H.
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container_end_page 1717
container_issue 6
container_start_page 1707
container_title Magnetic resonance in medicine
container_volume 70
creator Szulc, Kamila U.
Nieman, Brian J.
Houston, Edward J.
Bartelle, Benjamin B.
Lerch, Jason P.
Joyner, Alexandra L.
Turnbull, Daniel H.
description 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.
doi_str_mv 10.1002/mrm.24597
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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.</description><identifier>ISSN: 0740-3194</identifier><identifier>EISSN: 1522-2594</identifier><identifier>DOI: 10.1002/mrm.24597</identifier><identifier>PMID: 23400959</identifier><identifier>CODEN: MRMEEN</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Animal models ; Animals ; Animals, Newborn ; brain development ; cerebellum ; Cerebellum - abnormalities ; Cerebellum - growth &amp; development ; Cerebellum - pathology ; Cerebellum - physiopathology ; Developmental Disabilities - genetics ; Developmental Disabilities - pathology ; Developmental Disabilities - physiopathology ; gastrulation brain homeobox 2 gene (Gbx2) ; Homeodomain Proteins - genetics ; Magnetic Resonance Imaging - methods ; manganese-enhanced MRI (MEMRI) ; Mice ; Mice, Knockout ; mid-hindbrain ; Nervous System Malformations - genetics ; Nervous System Malformations - pathology ; Nervous System Malformations - physiopathology ; Phenotype ; Reproducibility of Results ; Sensitivity and Specificity ; Vestibule, Labyrinth - abnormalities ; Vestibule, Labyrinth - growth &amp; development ; Vestibule, Labyrinth - pathology ; vestibulo-cochlear organ</subject><ispartof>Magnetic resonance in medicine, 2013-12, Vol.70 (6), p.1707-1717</ispartof><rights>Copyright © 2013 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5807-20ea226ffdcd5ad2ad5dd10ca2eab4ea8f675a7f2eec2604b7fc4aee7d6d421e3</citedby><cites>FETCH-LOGICAL-c5807-20ea226ffdcd5ad2ad5dd10ca2eab4ea8f675a7f2eec2604b7fc4aee7d6d421e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmrm.24597$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmrm.24597$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23400959$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Szulc, Kamila U.</creatorcontrib><creatorcontrib>Nieman, Brian J.</creatorcontrib><creatorcontrib>Houston, Edward J.</creatorcontrib><creatorcontrib>Bartelle, Benjamin B.</creatorcontrib><creatorcontrib>Lerch, Jason P.</creatorcontrib><creatorcontrib>Joyner, Alexandra L.</creatorcontrib><creatorcontrib>Turnbull, Daniel H.</creatorcontrib><title>MRI analysis of cerebellar and vestibular developmental phenotypes in Gbx2 conditional knockout mice</title><title>Magnetic resonance in medicine</title><addtitle>Magn. Reson. Med</addtitle><description>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. 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Reson. Med</addtitle><date>2013-12</date><risdate>2013</risdate><volume>70</volume><issue>6</issue><spage>1707</spage><epage>1717</epage><pages>1707-1717</pages><issn>0740-3194</issn><eissn>1522-2594</eissn><coden>MRMEEN</coden><abstract>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. 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subjects Animal models
Animals
Animals, Newborn
brain development
cerebellum
Cerebellum - abnormalities
Cerebellum - growth & development
Cerebellum - pathology
Cerebellum - physiopathology
Developmental Disabilities - genetics
Developmental Disabilities - pathology
Developmental Disabilities - physiopathology
gastrulation brain homeobox 2 gene (Gbx2)
Homeodomain Proteins - genetics
Magnetic Resonance Imaging - methods
manganese-enhanced MRI (MEMRI)
Mice
Mice, Knockout
mid-hindbrain
Nervous System Malformations - genetics
Nervous System Malformations - pathology
Nervous System Malformations - physiopathology
Phenotype
Reproducibility of Results
Sensitivity and Specificity
Vestibule, Labyrinth - abnormalities
Vestibule, Labyrinth - growth & development
Vestibule, Labyrinth - pathology
vestibulo-cochlear organ
title MRI analysis of cerebellar and vestibular developmental phenotypes in Gbx2 conditional knockout mice
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