Cerebellar Purkinje Cells are Reduced in a Subpopulation of Autistic Brains: A Stereological Experiment Using Calbindin-D28k
Although a decreased number of cerebellar Purkinje cells (PCs) in the autistic brain has been widely reported with a variety of qualitative and quantitative methods, the more accurate method of cell counting with modern stereology has not yet been employed. An additional possible problem with prior...
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description | Although a decreased number of cerebellar Purkinje cells (PCs) in the autistic brain has been widely reported with a variety of qualitative and quantitative methods, the more accurate method of cell counting with modern stereology has not yet been employed. An additional possible problem with prior reports is the use of Nissl staining to identify the PCs, as this can miss cells due to staining irregularities. In the present study, PCs were immunostained for calbindin-D28k (CB), as this has been shown to be a more reliable marker for PCs than the Nissl stain, with more than 99% of the PCs immunopositive (Whitney, Kemper, Rosene, Bauman, Blatt, J Neurosci Methods 168:42–47,
2008
). Using stereology and CB immunostaining, the density of PCs was determined in serial sections from a consistently defined area of the cerebellar hemisphere in four control and six autistic brains, with the density of PCs then correlated with the clinical severity of autism. Overall, there was no significant difference in the density of PCs between the autistic and control groups. However, three of six autistic brains had PC numbers that fell within the control range, whereas the remaining three autistic brains revealed a reduction compared with the control brains. These data demonstrate that a reduction in cerebellar PCs was not a consistent feature of these autistic brains and that it occurred without discernible correlation between their density and the clinical features or severity of autism. |
doi_str_mv | 10.1007/s12311-008-0043-y |
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2008
). Using stereology and CB immunostaining, the density of PCs was determined in serial sections from a consistently defined area of the cerebellar hemisphere in four control and six autistic brains, with the density of PCs then correlated with the clinical severity of autism. Overall, there was no significant difference in the density of PCs between the autistic and control groups. However, three of six autistic brains had PC numbers that fell within the control range, whereas the remaining three autistic brains revealed a reduction compared with the control brains. These data demonstrate that a reduction in cerebellar PCs was not a consistent feature of these autistic brains and that it occurred without discernible correlation between their density and the clinical features or severity of autism.</description><identifier>ISSN: 1473-4222</identifier><identifier>EISSN: 1473-4230</identifier><identifier>DOI: 10.1007/s12311-008-0043-y</identifier><identifier>PMID: 18587625</identifier><language>eng</language><publisher>New York: Springer-Verlag</publisher><subject>Adolescent ; Adult ; Autistic Disorder - genetics ; Biomarkers - metabolism ; Biomedical and Life Sciences ; Biomedicine ; Brain - pathology ; Calbindin 1 ; Calbindins ; Cerebellum - pathology ; Cerebellum - physiology ; Female ; Humans ; Male ; Middle Aged ; Neurobiology ; Neurology ; Neurosciences ; Purkinje Cells - pathology ; Purkinje Cells - physiology ; Reference Values ; S100 Calcium Binding Protein G - metabolism ; Severity of Illness Index ; Young Adult</subject><ispartof>Cerebellum (London, England), 2008-09, Vol.7 (3), p.406-416</ispartof><rights>Springer Science+Business Media, LLC 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12311-008-0043-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12311-008-0043-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18587625$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Whitney, Elizabeth R.</creatorcontrib><creatorcontrib>Kemper, Thomas L.</creatorcontrib><creatorcontrib>Bauman, Margaret L.</creatorcontrib><creatorcontrib>Rosene, Douglas L.</creatorcontrib><creatorcontrib>Blatt, Gene J.</creatorcontrib><title>Cerebellar Purkinje Cells are Reduced in a Subpopulation of Autistic Brains: A Stereological Experiment Using Calbindin-D28k</title><title>Cerebellum (London, England)</title><addtitle>Cerebellum</addtitle><addtitle>Cerebellum</addtitle><description>Although a decreased number of cerebellar Purkinje cells (PCs) in the autistic brain has been widely reported with a variety of qualitative and quantitative methods, the more accurate method of cell counting with modern stereology has not yet been employed. An additional possible problem with prior reports is the use of Nissl staining to identify the PCs, as this can miss cells due to staining irregularities. In the present study, PCs were immunostained for calbindin-D28k (CB), as this has been shown to be a more reliable marker for PCs than the Nissl stain, with more than 99% of the PCs immunopositive (Whitney, Kemper, Rosene, Bauman, Blatt, J Neurosci Methods 168:42–47,
2008
). Using stereology and CB immunostaining, the density of PCs was determined in serial sections from a consistently defined area of the cerebellar hemisphere in four control and six autistic brains, with the density of PCs then correlated with the clinical severity of autism. Overall, there was no significant difference in the density of PCs between the autistic and control groups. However, three of six autistic brains had PC numbers that fell within the control range, whereas the remaining three autistic brains revealed a reduction compared with the control brains. These data demonstrate that a reduction in cerebellar PCs was not a consistent feature of these autistic brains and that it occurred without discernible correlation between their density and the clinical features or severity of autism.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Autistic Disorder - genetics</subject><subject>Biomarkers - metabolism</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain - pathology</subject><subject>Calbindin 1</subject><subject>Calbindins</subject><subject>Cerebellum - pathology</subject><subject>Cerebellum - physiology</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neurobiology</subject><subject>Neurology</subject><subject>Neurosciences</subject><subject>Purkinje Cells - pathology</subject><subject>Purkinje Cells - physiology</subject><subject>Reference Values</subject><subject>S100 Calcium Binding Protein G - metabolism</subject><subject>Severity of Illness Index</subject><subject>Young Adult</subject><issn>1473-4222</issn><issn>1473-4230</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpNkdtKAzEQhoMoth4ewBsJeL2aw-5m17u61gMUFGuvQ7LJlrTb7JpswIIPb0pVvBhmhvn5ZpgfgAuMrjFC7MZjQjFOECpipDTZHoAxThlNUkLR4V9NyAiceL9CiBCUsmMwwkVWsJxkY_BVaaelblvh4Gtwa2NXGlax91A4Dd-0CrVW0Fgo4DzIvutDKwbTWdg1cBIG4wdTwzsnjPW3cALnQ-R1bbc0tWjh9LPXzmy0HeDCG7uElWilscrY5J4U6zNw1IjW6_OffAoWD9P36imZvTw-V5NZ0mNWDgktGMZMSiYUEyjFNG9EWZA8y3KEmwYLWmQEibJUIs-bulYybZhiUpRM0bLW9BRc7bm96z6C9gNfdcHZuJJjHH-YRz6KqssfVZAbrXgfLxduy3-fFQVkL_BxZJfa_cMgvnOE7x3h0RG-c4Rv6TfIrHxG</recordid><startdate>20080901</startdate><enddate>20080901</enddate><creator>Whitney, Elizabeth R.</creator><creator>Kemper, Thomas L.</creator><creator>Bauman, Margaret L.</creator><creator>Rosene, Douglas L.</creator><creator>Blatt, Gene J.</creator><general>Springer-Verlag</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope></search><sort><creationdate>20080901</creationdate><title>Cerebellar Purkinje Cells are Reduced in a Subpopulation of Autistic Brains: A Stereological Experiment Using Calbindin-D28k</title><author>Whitney, Elizabeth R. ; Kemper, Thomas L. ; Bauman, Margaret L. ; Rosene, Douglas L. ; Blatt, Gene J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p179t-387117bb7ad7a04136fa982655601ff1a38520a99da66fccdb4f7d7ba97d39ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Autistic Disorder - genetics</topic><topic>Biomarkers - metabolism</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brain - pathology</topic><topic>Calbindin 1</topic><topic>Calbindins</topic><topic>Cerebellum - pathology</topic><topic>Cerebellum - physiology</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neurobiology</topic><topic>Neurology</topic><topic>Neurosciences</topic><topic>Purkinje Cells - pathology</topic><topic>Purkinje Cells - physiology</topic><topic>Reference Values</topic><topic>S100 Calcium Binding Protein G - metabolism</topic><topic>Severity of Illness Index</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Whitney, Elizabeth R.</creatorcontrib><creatorcontrib>Kemper, Thomas L.</creatorcontrib><creatorcontrib>Bauman, Margaret L.</creatorcontrib><creatorcontrib>Rosene, Douglas L.</creatorcontrib><creatorcontrib>Blatt, Gene J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><jtitle>Cerebellum (London, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Whitney, Elizabeth R.</au><au>Kemper, Thomas L.</au><au>Bauman, Margaret L.</au><au>Rosene, Douglas L.</au><au>Blatt, Gene J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cerebellar Purkinje Cells are Reduced in a Subpopulation of Autistic Brains: A Stereological Experiment Using Calbindin-D28k</atitle><jtitle>Cerebellum (London, England)</jtitle><stitle>Cerebellum</stitle><addtitle>Cerebellum</addtitle><date>2008-09-01</date><risdate>2008</risdate><volume>7</volume><issue>3</issue><spage>406</spage><epage>416</epage><pages>406-416</pages><issn>1473-4222</issn><eissn>1473-4230</eissn><abstract>Although a decreased number of cerebellar Purkinje cells (PCs) in the autistic brain has been widely reported with a variety of qualitative and quantitative methods, the more accurate method of cell counting with modern stereology has not yet been employed. An additional possible problem with prior reports is the use of Nissl staining to identify the PCs, as this can miss cells due to staining irregularities. In the present study, PCs were immunostained for calbindin-D28k (CB), as this has been shown to be a more reliable marker for PCs than the Nissl stain, with more than 99% of the PCs immunopositive (Whitney, Kemper, Rosene, Bauman, Blatt, J Neurosci Methods 168:42–47,
2008
). Using stereology and CB immunostaining, the density of PCs was determined in serial sections from a consistently defined area of the cerebellar hemisphere in four control and six autistic brains, with the density of PCs then correlated with the clinical severity of autism. Overall, there was no significant difference in the density of PCs between the autistic and control groups. However, three of six autistic brains had PC numbers that fell within the control range, whereas the remaining three autistic brains revealed a reduction compared with the control brains. These data demonstrate that a reduction in cerebellar PCs was not a consistent feature of these autistic brains and that it occurred without discernible correlation between their density and the clinical features or severity of autism.</abstract><cop>New York</cop><pub>Springer-Verlag</pub><pmid>18587625</pmid><doi>10.1007/s12311-008-0043-y</doi><tpages>11</tpages></addata></record> |
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subjects | Adolescent Adult Autistic Disorder - genetics Biomarkers - metabolism Biomedical and Life Sciences Biomedicine Brain - pathology Calbindin 1 Calbindins Cerebellum - pathology Cerebellum - physiology Female Humans Male Middle Aged Neurobiology Neurology Neurosciences Purkinje Cells - pathology Purkinje Cells - physiology Reference Values S100 Calcium Binding Protein G - metabolism Severity of Illness Index Young Adult |
title | Cerebellar Purkinje Cells are Reduced in a Subpopulation of Autistic Brains: A Stereological Experiment Using Calbindin-D28k |
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