Structural and immunohistological modifications in olfactory bulb of the staggerer mutant mouse
In the present study, we describe the structural and cytological changes observed in staggerer mutant olfactory bulbs, as compared to normal mice. On the basis of photonic and ultrastructural observations we tried to define the alterations induced by the mutation: ie a reduction of bulb size, a redu...
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Veröffentlicht in: | Biology of the cell 1999, Vol.91 (1), p.29-44 |
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creator | Monnier, Zoré Bahjaoui-Bouhaddi, Malika Bride, Jacqueline Bride, Michelle Math, François Propper, Alain |
description | In the present study, we describe the structural and cytological changes observed in
staggerer mutant olfactory bulbs, as compared to normal mice. On the basis of photonic and ultrastructural observations we tried to define the alterations induced by the mutation:
ie a reduction of bulb size, a reduction in the volume of three out of the six architectonic layers (glomerular, external and internal plexiform), a reduction of glomeruli size, a loss of half the mitral cells and a slight decrease in juxtaglomerular interneuron number. In
staggerer, an hypertrophy of glial ensheathing cell processes was especially evident at the level of each glomerulus, whereas the density of the astrocyte network was weaker in the granular layer and the nerve layer not apparently impaired. An immunofluorescent labelling study combined with confocal scanning microscopy was performed in order to identify the cellular type and the differentiation degree of the various elements. Antibodies anti-GFAP, a protein present in both ensheathing cells and astrocytes, and anti-OMP, the specific maturation protein of the nerve layer, were used for that purpose. Data confirmed the reality of the gliosis and the persistence of the sensory component in the mutant. All the structural alterations described in
staggerer olfactory bulb were in close agreement with the functional troubles previously recorded. Our results are discussed in connection with the present knowledge on embryonal origin, fetal development and adult cellular renewal of the olfactory bulb. |
doi_str_mv | 10.1016/S0248-4900(99)80028-8 |
format | Article |
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staggerer mutant olfactory bulbs, as compared to normal mice. On the basis of photonic and ultrastructural observations we tried to define the alterations induced by the mutation:
ie a reduction of bulb size, a reduction in the volume of three out of the six architectonic layers (glomerular, external and internal plexiform), a reduction of glomeruli size, a loss of half the mitral cells and a slight decrease in juxtaglomerular interneuron number. In
staggerer, an hypertrophy of glial ensheathing cell processes was especially evident at the level of each glomerulus, whereas the density of the astrocyte network was weaker in the granular layer and the nerve layer not apparently impaired. An immunofluorescent labelling study combined with confocal scanning microscopy was performed in order to identify the cellular type and the differentiation degree of the various elements. Antibodies anti-GFAP, a protein present in both ensheathing cells and astrocytes, and anti-OMP, the specific maturation protein of the nerve layer, were used for that purpose. Data confirmed the reality of the gliosis and the persistence of the sensory component in the mutant. All the structural alterations described in
staggerer olfactory bulb were in close agreement with the functional troubles previously recorded. Our results are discussed in connection with the present knowledge on embryonal origin, fetal development and adult cellular renewal of the olfactory bulb.</description><identifier>ISSN: 0248-4900</identifier><identifier>EISSN: 1768-322X</identifier><identifier>DOI: 10.1016/S0248-4900(99)80028-8</identifier><identifier>PMID: 10321020</identifier><language>eng</language><publisher>England: Elsevier SAS</publisher><subject>Animals ; Biomarkers ; Cell Count ; Cell Differentiation ; Cerebellar Diseases - genetics ; Cerebellar Diseases - pathology ; electron-confocal microscopy ; Gene Deletion ; GFAP ; Glial Fibrillary Acidic Protein - analysis ; immunolabelling ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Neurologic Mutants - anatomy & histology ; Microscopy, Confocal ; Microscopy, Electron ; Microscopy, Fluorescence ; Nerve Degeneration - genetics ; Nerve Degeneration - pathology ; Nerve Tissue Proteins - analysis ; Neuroglia - pathology ; Nuclear Receptor Subfamily 1, Group F, Member 1 ; olfactory bulb ; Olfactory Bulb - pathology ; Olfactory Marker Protein ; Olfactory Nerve - pathology ; OMP ; Receptors, Cytoplasmic and Nuclear - deficiency ; Receptors, Cytoplasmic and Nuclear - genetics ; Trans-Activators - deficiency ; Trans-Activators - genetics</subject><ispartof>Biology of the cell, 1999, Vol.91 (1), p.29-44</ispartof><rights>1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c315t-aa769cb5bf71c4599affe91298da9e30a28a8778c4e891baac74b832565382bb3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10321020$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Monnier, Zoré</creatorcontrib><creatorcontrib>Bahjaoui-Bouhaddi, Malika</creatorcontrib><creatorcontrib>Bride, Jacqueline</creatorcontrib><creatorcontrib>Bride, Michelle</creatorcontrib><creatorcontrib>Math, François</creatorcontrib><creatorcontrib>Propper, Alain</creatorcontrib><title>Structural and immunohistological modifications in olfactory bulb of the staggerer mutant mouse</title><title>Biology of the cell</title><addtitle>Biol Cell</addtitle><description>In the present study, we describe the structural and cytological changes observed in
staggerer mutant olfactory bulbs, as compared to normal mice. On the basis of photonic and ultrastructural observations we tried to define the alterations induced by the mutation:
ie a reduction of bulb size, a reduction in the volume of three out of the six architectonic layers (glomerular, external and internal plexiform), a reduction of glomeruli size, a loss of half the mitral cells and a slight decrease in juxtaglomerular interneuron number. In
staggerer, an hypertrophy of glial ensheathing cell processes was especially evident at the level of each glomerulus, whereas the density of the astrocyte network was weaker in the granular layer and the nerve layer not apparently impaired. An immunofluorescent labelling study combined with confocal scanning microscopy was performed in order to identify the cellular type and the differentiation degree of the various elements. Antibodies anti-GFAP, a protein present in both ensheathing cells and astrocytes, and anti-OMP, the specific maturation protein of the nerve layer, were used for that purpose. Data confirmed the reality of the gliosis and the persistence of the sensory component in the mutant. All the structural alterations described in
staggerer olfactory bulb were in close agreement with the functional troubles previously recorded. Our results are discussed in connection with the present knowledge on embryonal origin, fetal development and adult cellular renewal of the olfactory bulb.</description><subject>Animals</subject><subject>Biomarkers</subject><subject>Cell Count</subject><subject>Cell Differentiation</subject><subject>Cerebellar Diseases - genetics</subject><subject>Cerebellar Diseases - pathology</subject><subject>electron-confocal microscopy</subject><subject>Gene Deletion</subject><subject>GFAP</subject><subject>Glial Fibrillary Acidic Protein - analysis</subject><subject>immunolabelling</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Neurologic Mutants - anatomy & histology</subject><subject>Microscopy, Confocal</subject><subject>Microscopy, Electron</subject><subject>Microscopy, Fluorescence</subject><subject>Nerve Degeneration - genetics</subject><subject>Nerve Degeneration - pathology</subject><subject>Nerve Tissue Proteins - analysis</subject><subject>Neuroglia - pathology</subject><subject>Nuclear Receptor Subfamily 1, Group F, Member 1</subject><subject>olfactory bulb</subject><subject>Olfactory Bulb - pathology</subject><subject>Olfactory Marker Protein</subject><subject>Olfactory Nerve - pathology</subject><subject>OMP</subject><subject>Receptors, Cytoplasmic and Nuclear - deficiency</subject><subject>Receptors, Cytoplasmic and Nuclear - genetics</subject><subject>Trans-Activators - deficiency</subject><subject>Trans-Activators - genetics</subject><issn>0248-4900</issn><issn>1768-322X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kUtLAzEUhYMoWqs_QclKdDGaxzySlUjxBQUXVXAXksydNjIz0SQj9N87rdXVvVy-czmcg9AZJdeU0PJmQVguslwScinllSCEiUzsoQmtSpFxxt730eQfOULHMX4QQnIpikN0RAlnlDAyQWqRwmDTEHSLdV9j13VD71cuJt_6pbPjufO1a8YtOd9H7Hrs20bb5MMam6E12Dc4rQDHpJdLCBBwNyTdp1E3RDhBB41uI5zu5hS9Pdy_zp6y-cvj8-xunllOi5RpXZXSmsI0FbV5IaVuGpCUSVFrCZxoJrSoKmFzEJIarW2VG8FZURZcMGP4FF38_v0M_muAmFTnooW21T2MPlQpq7wUgo_g-Q4cTAe1-gyu02Gt_iIZgdtfAEa73w6CitZBb6F2AWxStXcjrDYlqG0JapOwklJtS1CC_wC9M3px</recordid><startdate>1999</startdate><enddate>1999</enddate><creator>Monnier, Zoré</creator><creator>Bahjaoui-Bouhaddi, Malika</creator><creator>Bride, Jacqueline</creator><creator>Bride, Michelle</creator><creator>Math, François</creator><creator>Propper, Alain</creator><general>Elsevier SAS</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>1999</creationdate><title>Structural and immunohistological modifications in olfactory bulb of the staggerer mutant mouse</title><author>Monnier, Zoré ; Bahjaoui-Bouhaddi, Malika ; Bride, Jacqueline ; Bride, Michelle ; Math, François ; Propper, Alain</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c315t-aa769cb5bf71c4599affe91298da9e30a28a8778c4e891baac74b832565382bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Biomarkers</topic><topic>Cell Count</topic><topic>Cell Differentiation</topic><topic>Cerebellar Diseases - genetics</topic><topic>Cerebellar Diseases - pathology</topic><topic>electron-confocal microscopy</topic><topic>Gene Deletion</topic><topic>GFAP</topic><topic>Glial Fibrillary Acidic Protein - analysis</topic><topic>immunolabelling</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Neurologic Mutants - anatomy & histology</topic><topic>Microscopy, Confocal</topic><topic>Microscopy, Electron</topic><topic>Microscopy, Fluorescence</topic><topic>Nerve Degeneration - genetics</topic><topic>Nerve Degeneration - pathology</topic><topic>Nerve Tissue Proteins - analysis</topic><topic>Neuroglia - pathology</topic><topic>Nuclear Receptor Subfamily 1, Group F, Member 1</topic><topic>olfactory bulb</topic><topic>Olfactory Bulb - pathology</topic><topic>Olfactory Marker Protein</topic><topic>Olfactory Nerve - pathology</topic><topic>OMP</topic><topic>Receptors, Cytoplasmic and Nuclear - deficiency</topic><topic>Receptors, Cytoplasmic and Nuclear - genetics</topic><topic>Trans-Activators - deficiency</topic><topic>Trans-Activators - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Monnier, Zoré</creatorcontrib><creatorcontrib>Bahjaoui-Bouhaddi, Malika</creatorcontrib><creatorcontrib>Bride, Jacqueline</creatorcontrib><creatorcontrib>Bride, Michelle</creatorcontrib><creatorcontrib>Math, François</creatorcontrib><creatorcontrib>Propper, Alain</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Biology of the cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Monnier, Zoré</au><au>Bahjaoui-Bouhaddi, Malika</au><au>Bride, Jacqueline</au><au>Bride, Michelle</au><au>Math, François</au><au>Propper, Alain</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural and immunohistological modifications in olfactory bulb of the staggerer mutant mouse</atitle><jtitle>Biology of the cell</jtitle><addtitle>Biol Cell</addtitle><date>1999</date><risdate>1999</risdate><volume>91</volume><issue>1</issue><spage>29</spage><epage>44</epage><pages>29-44</pages><issn>0248-4900</issn><eissn>1768-322X</eissn><abstract>In the present study, we describe the structural and cytological changes observed in
staggerer mutant olfactory bulbs, as compared to normal mice. On the basis of photonic and ultrastructural observations we tried to define the alterations induced by the mutation:
ie a reduction of bulb size, a reduction in the volume of three out of the six architectonic layers (glomerular, external and internal plexiform), a reduction of glomeruli size, a loss of half the mitral cells and a slight decrease in juxtaglomerular interneuron number. In
staggerer, an hypertrophy of glial ensheathing cell processes was especially evident at the level of each glomerulus, whereas the density of the astrocyte network was weaker in the granular layer and the nerve layer not apparently impaired. An immunofluorescent labelling study combined with confocal scanning microscopy was performed in order to identify the cellular type and the differentiation degree of the various elements. Antibodies anti-GFAP, a protein present in both ensheathing cells and astrocytes, and anti-OMP, the specific maturation protein of the nerve layer, were used for that purpose. Data confirmed the reality of the gliosis and the persistence of the sensory component in the mutant. All the structural alterations described in
staggerer olfactory bulb were in close agreement with the functional troubles previously recorded. Our results are discussed in connection with the present knowledge on embryonal origin, fetal development and adult cellular renewal of the olfactory bulb.</abstract><cop>England</cop><pub>Elsevier SAS</pub><pmid>10321020</pmid><doi>10.1016/S0248-4900(99)80028-8</doi><tpages>16</tpages></addata></record> |
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subjects | Animals Biomarkers Cell Count Cell Differentiation Cerebellar Diseases - genetics Cerebellar Diseases - pathology electron-confocal microscopy Gene Deletion GFAP Glial Fibrillary Acidic Protein - analysis immunolabelling Male Mice Mice, Inbred C57BL Mice, Neurologic Mutants - anatomy & histology Microscopy, Confocal Microscopy, Electron Microscopy, Fluorescence Nerve Degeneration - genetics Nerve Degeneration - pathology Nerve Tissue Proteins - analysis Neuroglia - pathology Nuclear Receptor Subfamily 1, Group F, Member 1 olfactory bulb Olfactory Bulb - pathology Olfactory Marker Protein Olfactory Nerve - pathology OMP Receptors, Cytoplasmic and Nuclear - deficiency Receptors, Cytoplasmic and Nuclear - genetics Trans-Activators - deficiency Trans-Activators - genetics |
title | Structural and immunohistological modifications in olfactory bulb of the staggerer mutant mouse |
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