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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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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3657598</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3128926231</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5807-20ea226ffdcd5ad2ad5dd10ca2eab4ea8f675a7f2eec2604b7fc4aee7d6d421e3</originalsourceid><addsrcrecordid>eNqNkc1u1DAUhS0EotPCghdAkdjQRVrbseNkg1RVMFR0yqgCdWk59g11J4mDnQydt8ch7QiQkFj577vH956D0CuCTwjG9LT17QllvBRP0IJwSlPKS_YULbBgOM1IyQ7QYQh3GOOyFOw5OqAZi3teLpBZXV8kqlPNLtiQuDrR4KGCplE-XptkC2Gw1TgdDWyhcX0L3aCapL-Fzg27HkJiu2RZ3dNEu87Ywbqolmw6pzduHJLWaniBntWqCfDyYT1CXz-8_3L-Mb38vLw4P7tMNS-wSCkGRWle10YbrgxVhhtDsFYUVMVAFXUuuBI1BdA0x6wStWYKQJjcMEogO0LvZt1-rFowOnbqVSN7b1vld9IpK_986eyt_Oa2Msu54GURBd4-CHj3fYyjy9YGPbnRgRuDJCwvMk4YLf8D5ZPZMZ6IvvkLvXOjjy7NFMk5K6a_j2dKexeCh3rfN8FyilnGmOWvmCP7-vdB9-RjrhE4nYEftoHdv5Xk6nr1KJnOFTYMcL-vUH4jc5EJLm-ulnK9vllf8U9E8uwn-6XD4w</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1459165488</pqid></control><display><type>article</type><title>MRI analysis of cerebellar and vestibular developmental phenotypes in Gbx2 conditional knockout mice</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Wiley Online Library Free Content</source><creator>Szulc, Kamila U. ; Nieman, Brian J. ; Houston, Edward J. ; Bartelle, Benjamin B. ; Lerch, Jason P. ; Joyner, Alexandra L. ; Turnbull, Daniel H.</creator><creatorcontrib>Szulc, Kamila U. ; Nieman, Brian J. ; Houston, Edward J. ; Bartelle, Benjamin B. ; Lerch, Jason P. ; Joyner, Alexandra L. ; Turnbull, Daniel H.</creatorcontrib><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.</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 & 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</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. Magn Reson Med 70:1707–1717, 2013. © 2013 Wiley Periodicals, Inc.</description><subject>Animal models</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>brain development</subject><subject>cerebellum</subject><subject>Cerebellum - abnormalities</subject><subject>Cerebellum - growth & development</subject><subject>Cerebellum - pathology</subject><subject>Cerebellum - physiopathology</subject><subject>Developmental Disabilities - genetics</subject><subject>Developmental Disabilities - pathology</subject><subject>Developmental Disabilities - physiopathology</subject><subject>gastrulation brain homeobox 2 gene (Gbx2)</subject><subject>Homeodomain Proteins - genetics</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>manganese-enhanced MRI (MEMRI)</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>mid-hindbrain</subject><subject>Nervous System Malformations - genetics</subject><subject>Nervous System Malformations - pathology</subject><subject>Nervous System Malformations - physiopathology</subject><subject>Phenotype</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><subject>Vestibule, Labyrinth - abnormalities</subject><subject>Vestibule, Labyrinth - growth & development</subject><subject>Vestibule, Labyrinth - pathology</subject><subject>vestibulo-cochlear organ</subject><issn>0740-3194</issn><issn>1522-2594</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAUhS0EotPCghdAkdjQRVrbseNkg1RVMFR0yqgCdWk59g11J4mDnQydt8ch7QiQkFj577vH956D0CuCTwjG9LT17QllvBRP0IJwSlPKS_YULbBgOM1IyQ7QYQh3GOOyFOw5OqAZi3teLpBZXV8kqlPNLtiQuDrR4KGCplE-XptkC2Gw1TgdDWyhcX0L3aCapL-Fzg27HkJiu2RZ3dNEu87Ywbqolmw6pzduHJLWaniBntWqCfDyYT1CXz-8_3L-Mb38vLw4P7tMNS-wSCkGRWle10YbrgxVhhtDsFYUVMVAFXUuuBI1BdA0x6wStWYKQJjcMEogO0LvZt1-rFowOnbqVSN7b1vld9IpK_986eyt_Oa2Msu54GURBd4-CHj3fYyjy9YGPbnRgRuDJCwvMk4YLf8D5ZPZMZ6IvvkLvXOjjy7NFMk5K6a_j2dKexeCh3rfN8FyilnGmOWvmCP7-vdB9-RjrhE4nYEftoHdv5Xk6nr1KJnOFTYMcL-vUH4jc5EJLm-ulnK9vllf8U9E8uwn-6XD4w</recordid><startdate>201312</startdate><enddate>201312</enddate><creator>Szulc, Kamila U.</creator><creator>Nieman, Brian J.</creator><creator>Houston, Edward J.</creator><creator>Bartelle, Benjamin B.</creator><creator>Lerch, Jason P.</creator><creator>Joyner, Alexandra L.</creator><creator>Turnbull, Daniel H.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope><scope>7QO</scope><scope>7TK</scope><scope>5PM</scope></search><sort><creationdate>201312</creationdate><title>MRI analysis of cerebellar and vestibular developmental phenotypes in Gbx2 conditional knockout mice</title><author>Szulc, Kamila U. ; Nieman, Brian J. ; Houston, Edward J. ; Bartelle, Benjamin B. ; Lerch, Jason P. ; Joyner, Alexandra L. ; Turnbull, Daniel H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5807-20ea226ffdcd5ad2ad5dd10ca2eab4ea8f675a7f2eec2604b7fc4aee7d6d421e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animal models</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>brain development</topic><topic>cerebellum</topic><topic>Cerebellum - abnormalities</topic><topic>Cerebellum - growth & development</topic><topic>Cerebellum - pathology</topic><topic>Cerebellum - physiopathology</topic><topic>Developmental Disabilities - genetics</topic><topic>Developmental Disabilities - pathology</topic><topic>Developmental Disabilities - physiopathology</topic><topic>gastrulation brain homeobox 2 gene (Gbx2)</topic><topic>Homeodomain Proteins - genetics</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>manganese-enhanced MRI (MEMRI)</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>mid-hindbrain</topic><topic>Nervous System Malformations - genetics</topic><topic>Nervous System Malformations - pathology</topic><topic>Nervous System Malformations - physiopathology</topic><topic>Phenotype</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><topic>Vestibule, Labyrinth - abnormalities</topic><topic>Vestibule, Labyrinth - growth & development</topic><topic>Vestibule, Labyrinth - pathology</topic><topic>vestibulo-cochlear organ</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Magnetic resonance in medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Szulc, Kamila U.</au><au>Nieman, Brian J.</au><au>Houston, Edward J.</au><au>Bartelle, Benjamin B.</au><au>Lerch, Jason P.</au><au>Joyner, Alexandra L.</au><au>Turnbull, Daniel H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MRI analysis of cerebellar and vestibular developmental phenotypes in Gbx2 conditional knockout mice</atitle><jtitle>Magnetic resonance in medicine</jtitle><addtitle>Magn. 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. Magn Reson Med 70:1707–1717, 2013. © 2013 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>23400959</pmid><doi>10.1002/mrm.24597</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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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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