Aging-Associated Modulation in the Expression of Pax6 in Mouse Brain
Symptoms like mental retardation, depression, and anxiety have been observed during aging. Almost similar phenotypes have been evident in patients having haploinsufficiency or mutations in Pax6, a transcriptional regulator. Since Pax6 regulates axon guidance, differentiation of neurons from glia, an...
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Veröffentlicht in: | Cellular and molecular neurobiology 2012-03, Vol.32 (2), p.209-218 |
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description | Symptoms like mental retardation, depression, and anxiety have been observed during aging. Almost similar phenotypes have been evident in patients having haploinsufficiency or mutations in Pax6, a transcriptional regulator. Since Pax6 regulates axon guidance, differentiation of neurons from glia, and neuronal migration, it has been considered as a marker of newly generated neurons. The immunohistochemical analysis of Pax6 positive cells and expression pattern of Pax6 in olfactory lobe, hippocampus, and cerebellum of aging mouse brain have been investigated. The number of Pax6 positive cells and level of Pax6 were reduced progressively in olfactory lobe, cerebellum, and hippocampus from postnatal day-zero (P0) to old age mice. Pax6 positive cells were significantly lower in dentate gyrus, CA1, CA2, and CA3 regions of hippocampus, in mitral cell (MiCe), and internal plexiform (InPl) layers of olfactory lobe, and in granular cell (GrLa), and Purkinje’s cell (PuCe) layers of cerebellum from P0 to old age. Thus, modulation in the expression of Pax6 and reduction in Pax6 positive cells show direct association of Pax6 with aging-related neuronal dystrophy. |
doi_str_mv | 10.1007/s10571-011-9749-3 |
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Almost similar phenotypes have been evident in patients having haploinsufficiency or mutations in Pax6, a transcriptional regulator. Since Pax6 regulates axon guidance, differentiation of neurons from glia, and neuronal migration, it has been considered as a marker of newly generated neurons. The immunohistochemical analysis of Pax6 positive cells and expression pattern of Pax6 in olfactory lobe, hippocampus, and cerebellum of aging mouse brain have been investigated. The number of Pax6 positive cells and level of Pax6 were reduced progressively in olfactory lobe, cerebellum, and hippocampus from postnatal day-zero (P0) to old age mice. Pax6 positive cells were significantly lower in dentate gyrus, CA1, CA2, and CA3 regions of hippocampus, in mitral cell (MiCe), and internal plexiform (InPl) layers of olfactory lobe, and in granular cell (GrLa), and Purkinje’s cell (PuCe) layers of cerebellum from P0 to old age. Thus, modulation in the expression of Pax6 and reduction in Pax6 positive cells show direct association of Pax6 with aging-related neuronal dystrophy.</description><subject>Aging - metabolism</subject><subject>Aging - pathology</subject><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Blotting, Western</subject><subject>Brain - metabolism</subject><subject>Brain - pathology</subject><subject>Cell Biology</subject><subject>Cell Count</subject><subject>Eye Proteins - metabolism</subject><subject>Hippocampus - metabolism</subject><subject>Hippocampus - pathology</subject><subject>Homeodomain Proteins - metabolism</subject><subject>Immunohistochemistry</subject><subject>Mice</subject><subject>Neurobiology</subject><subject>Neurosciences</subject><subject>Organ Specificity</subject><subject>Original Research</subject><subject>Paired Box Transcription Factors - metabolism</subject><subject>PAX6 Transcription Factor</subject><subject>Repressor Proteins - metabolism</subject><issn>0272-4340</issn><issn>1573-6830</issn><issn>1573-6830</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kDtPwzAQxy0EouXxAVhQNibDXRwn8VhKeUitYIDZcpJzSZUmxU6k8u1JlMLIdNL9H7r7MXaFcIsAyZ1HkAlyQOQqiRQXR2yKMhE8TgUcsymEScgjEcGEnXm_AQAFIE_ZJEQFKBGm7GG2Lus1n3nf5KVpqQhWTdFVpi2bOijroP2kYLHfOfJ-2DQ2eDP7eFBWTecpuHemrC_YiTWVp8vDPGcfj4v3-TNfvj69zGdLnkegWp4lMrTKGpC5RIqNyClVlJFI4ziMIcPYqhRSI5WQFilNowiiiKzCoogzkuKc3Yy9O9d8deRbvS19TlVlauqv0SoMk75JYe_E0Zm7xntHVu9cuTXuWyPogZ0e2emenR7YadFnrg_tXbal4i_xC6s3hKPB91K9Jqc3Tefq_uN_Wn8AEaN4Eg</recordid><startdate>20120301</startdate><enddate>20120301</enddate><creator>Tripathi, Ratnakar</creator><creator>Mishra, Rajnikant</creator><general>Springer US</general><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>7X8</scope></search><sort><creationdate>20120301</creationdate><title>Aging-Associated Modulation in the Expression of Pax6 in Mouse Brain</title><author>Tripathi, Ratnakar ; Mishra, Rajnikant</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c409t-b752f9fa05c51e6a3ce89ebe3866260b16f9808a5935f1e8844044ef91dd6be53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Aging - metabolism</topic><topic>Aging - pathology</topic><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Blotting, Western</topic><topic>Brain - metabolism</topic><topic>Brain - pathology</topic><topic>Cell Biology</topic><topic>Cell Count</topic><topic>Eye Proteins - metabolism</topic><topic>Hippocampus - metabolism</topic><topic>Hippocampus - pathology</topic><topic>Homeodomain Proteins - metabolism</topic><topic>Immunohistochemistry</topic><topic>Mice</topic><topic>Neurobiology</topic><topic>Neurosciences</topic><topic>Organ Specificity</topic><topic>Original Research</topic><topic>Paired Box Transcription Factors - metabolism</topic><topic>PAX6 Transcription Factor</topic><topic>Repressor Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tripathi, Ratnakar</creatorcontrib><creatorcontrib>Mishra, Rajnikant</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cellular and molecular neurobiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tripathi, Ratnakar</au><au>Mishra, Rajnikant</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aging-Associated Modulation in the Expression of Pax6 in Mouse Brain</atitle><jtitle>Cellular and molecular neurobiology</jtitle><stitle>Cell Mol Neurobiol</stitle><addtitle>Cell Mol Neurobiol</addtitle><date>2012-03-01</date><risdate>2012</risdate><volume>32</volume><issue>2</issue><spage>209</spage><epage>218</epage><pages>209-218</pages><issn>0272-4340</issn><issn>1573-6830</issn><eissn>1573-6830</eissn><abstract>Symptoms like mental retardation, depression, and anxiety have been observed during aging. Almost similar phenotypes have been evident in patients having haploinsufficiency or mutations in Pax6, a transcriptional regulator. Since Pax6 regulates axon guidance, differentiation of neurons from glia, and neuronal migration, it has been considered as a marker of newly generated neurons. The immunohistochemical analysis of Pax6 positive cells and expression pattern of Pax6 in olfactory lobe, hippocampus, and cerebellum of aging mouse brain have been investigated. The number of Pax6 positive cells and level of Pax6 were reduced progressively in olfactory lobe, cerebellum, and hippocampus from postnatal day-zero (P0) to old age mice. Pax6 positive cells were significantly lower in dentate gyrus, CA1, CA2, and CA3 regions of hippocampus, in mitral cell (MiCe), and internal plexiform (InPl) layers of olfactory lobe, and in granular cell (GrLa), and Purkinje’s cell (PuCe) layers of cerebellum from P0 to old age. 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subjects | Aging - metabolism Aging - pathology Animals Biomedical and Life Sciences Biomedicine Blotting, Western Brain - metabolism Brain - pathology Cell Biology Cell Count Eye Proteins - metabolism Hippocampus - metabolism Hippocampus - pathology Homeodomain Proteins - metabolism Immunohistochemistry Mice Neurobiology Neurosciences Organ Specificity Original Research Paired Box Transcription Factors - metabolism PAX6 Transcription Factor Repressor Proteins - metabolism |
title | Aging-Associated Modulation in the Expression of Pax6 in Mouse Brain |
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