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Retinoic Acid Signaling Identifies a Distinct Precursor Population in the Developing and Adult Forebrain
We asked whether retinoic acid (RA), an established transcriptional regulator in regenerating and developing tissues, acts directly on distinct cell classes in the mature or embryonic forebrain. We identified a subset of slowly dividing precursors in the adult subventricular zone (SVZ) that is trans...
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Published in: | The Journal of neuroscience 2005-08, Vol.25 (33), p.7636-7647 |
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description | We asked whether retinoic acid (RA), an established transcriptional regulator in regenerating and developing tissues, acts directly on distinct cell classes in the mature or embryonic forebrain. We identified a subset of slowly dividing precursors in the adult subventricular zone (SVZ) that is transcriptionally activated by RA. Most of these cells express glial fibrillary acidic protein, a smaller subset expresses the epidermal growth factor receptor, a few are terminal deoxynucleotidyl transferase-mediated biotinylated UTP nick end labeling positive, and they can be mitotically labeled by sustained rather than acute bromodeoxyuridine exposure. RA activation in similar cells in SVZ-derived neurospheres depends on retinoid synthesis from the premetabolite retinol. The apparent influence of RA on precursors in vitro is consistent with key properties of RA activation in the SVZ; in neurospheres, altered retinoid signaling elicits neither cell death nor an acute increase in cell proliferation. There is apparent continuity of RA signaling in the forebrain throughout life. RA-activated, proliferative precursors with radial glial characteristics are found in the dorsal lateral ganglionic eminence and ventrolateral palliumembryonic rudiments of the SVZ. Thus, endogenous RA signaling distinguishes subsets of neural precursors with glial characteristics in a consistent region of the adult and developing forebrain. |
doi_str_mv | 10.1523/JNEUROSCI.0485-05.2005 |
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We identified a subset of slowly dividing precursors in the adult subventricular zone (SVZ) that is transcriptionally activated by RA. Most of these cells express glial fibrillary acidic protein, a smaller subset expresses the epidermal growth factor receptor, a few are terminal deoxynucleotidyl transferase-mediated biotinylated UTP nick end labeling positive, and they can be mitotically labeled by sustained rather than acute bromodeoxyuridine exposure. RA activation in similar cells in SVZ-derived neurospheres depends on retinoid synthesis from the premetabolite retinol. The apparent influence of RA on precursors in vitro is consistent with key properties of RA activation in the SVZ; in neurospheres, altered retinoid signaling elicits neither cell death nor an acute increase in cell proliferation. There is apparent continuity of RA signaling in the forebrain throughout life. RA-activated, proliferative precursors with radial glial characteristics are found in the dorsal lateral ganglionic eminence and ventrolateral palliumembryonic rudiments of the SVZ. 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We identified a subset of slowly dividing precursors in the adult subventricular zone (SVZ) that is transcriptionally activated by RA. Most of these cells express glial fibrillary acidic protein, a smaller subset expresses the epidermal growth factor receptor, a few are terminal deoxynucleotidyl transferase-mediated biotinylated UTP nick end labeling positive, and they can be mitotically labeled by sustained rather than acute bromodeoxyuridine exposure. RA activation in similar cells in SVZ-derived neurospheres depends on retinoid synthesis from the premetabolite retinol. The apparent influence of RA on precursors in vitro is consistent with key properties of RA activation in the SVZ; in neurospheres, altered retinoid signaling elicits neither cell death nor an acute increase in cell proliferation. There is apparent continuity of RA signaling in the forebrain throughout life. RA-activated, proliferative precursors with radial glial characteristics are found in the dorsal lateral ganglionic eminence and ventrolateral palliumembryonic rudiments of the SVZ. Thus, endogenous RA signaling distinguishes subsets of neural precursors with glial characteristics in a consistent region of the adult and developing forebrain.</description><subject>Aging - metabolism</subject><subject>Aging - physiology</subject><subject>Animals</subject><subject>Cell Differentiation - physiology</subject><subject>Cells, Cultured</subject><subject>Cellular/Molecular</subject><subject>Female</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>Mice, Transgenic</subject><subject>Pregnancy</subject><subject>Prosencephalon - cytology</subject><subject>Prosencephalon - embryology</subject><subject>Prosencephalon - growth & development</subject><subject>Prosencephalon - metabolism</subject><subject>Signal Transduction - physiology</subject><subject>Stem Cells - cytology</subject><subject>Stem Cells - metabolism</subject><subject>Tretinoin - physiology</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqFkcFu1DAQhi0EokvhFSqf4JRl7MR2ckFabVtYVNGqpWfLceyNkdde7KQr3p5Euypw4jSH-f5fM_oQuiCwJIyWH79-u3q8v31Yb5ZQ1awAtqQA7AVaTNumoBWQl2gBVEDBK1GdoTc5_wAAAUS8RmeEExCcwQL192ZwITqNV9p1-MFtg_IubPGmM2Fw1pmMFb50eaL0gO-S0WPKMeG7uB-9GlwM2AU89AZfmifj434Oq9DhVTf6AV_HZNqkXHiLXlnls3l3mufo8frq-_pLcXP7ebNe3RS6EmwoLG0JYZwYxlvbdYJZ1tKmYy3pQKhSV8o2lbWMqVLVNTEtaRWAhrbUgtpGlOfo07F3P7Y70-npi6S83Ce3U-mXjMrJfzfB9XIbnyQXlFWETgXvTwUp_hxNHuTOZW28V8HEMUteVw2h4v8gERWpGzqD_AjqFHNOxj5fQ0DONuWzTTnblMDkbHMKXvz9y5_YSd8EfDgCvdv2B5eMzDvl_YQTeTgcKJNlKQUvefkbtsKsQw</recordid><startdate>20050817</startdate><enddate>20050817</enddate><creator>Haskell, Gloria Thompson</creator><creator>LaMantia, Anthony-Samuel</creator><general>Soc Neuroscience</general><general>Society for Neuroscience</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>7TK</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20050817</creationdate><title>Retinoic Acid Signaling Identifies a Distinct Precursor Population in the Developing and Adult Forebrain</title><author>Haskell, Gloria Thompson ; LaMantia, Anthony-Samuel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-f2b11561e56bfdd75f5b29d5b1d07a3c4af94ff55a3a881eb1ba00c0b3c72f973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Aging - metabolism</topic><topic>Aging - physiology</topic><topic>Animals</topic><topic>Cell Differentiation - physiology</topic><topic>Cells, Cultured</topic><topic>Cellular/Molecular</topic><topic>Female</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred ICR</topic><topic>Mice, Transgenic</topic><topic>Pregnancy</topic><topic>Prosencephalon - cytology</topic><topic>Prosencephalon - embryology</topic><topic>Prosencephalon - growth & development</topic><topic>Prosencephalon - metabolism</topic><topic>Signal Transduction - physiology</topic><topic>Stem Cells - cytology</topic><topic>Stem Cells - metabolism</topic><topic>Tretinoin - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Haskell, Gloria Thompson</creatorcontrib><creatorcontrib>LaMantia, Anthony-Samuel</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Haskell, Gloria Thompson</au><au>LaMantia, Anthony-Samuel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Retinoic Acid Signaling Identifies a Distinct Precursor Population in the Developing and Adult Forebrain</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>2005-08-17</date><risdate>2005</risdate><volume>25</volume><issue>33</issue><spage>7636</spage><epage>7647</epage><pages>7636-7647</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>We asked whether retinoic acid (RA), an established transcriptional regulator in regenerating and developing tissues, acts directly on distinct cell classes in the mature or embryonic forebrain. We identified a subset of slowly dividing precursors in the adult subventricular zone (SVZ) that is transcriptionally activated by RA. Most of these cells express glial fibrillary acidic protein, a smaller subset expresses the epidermal growth factor receptor, a few are terminal deoxynucleotidyl transferase-mediated biotinylated UTP nick end labeling positive, and they can be mitotically labeled by sustained rather than acute bromodeoxyuridine exposure. RA activation in similar cells in SVZ-derived neurospheres depends on retinoid synthesis from the premetabolite retinol. The apparent influence of RA on precursors in vitro is consistent with key properties of RA activation in the SVZ; in neurospheres, altered retinoid signaling elicits neither cell death nor an acute increase in cell proliferation. There is apparent continuity of RA signaling in the forebrain throughout life. RA-activated, proliferative precursors with radial glial characteristics are found in the dorsal lateral ganglionic eminence and ventrolateral palliumembryonic rudiments of the SVZ. Thus, endogenous RA signaling distinguishes subsets of neural precursors with glial characteristics in a consistent region of the adult and developing forebrain.</abstract><cop>United States</cop><pub>Soc Neuroscience</pub><pmid>16107650</pmid><doi>10.1523/JNEUROSCI.0485-05.2005</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aging - metabolism Aging - physiology Animals Cell Differentiation - physiology Cells, Cultured Cellular/Molecular Female Male Mice Mice, Inbred ICR Mice, Transgenic Pregnancy Prosencephalon - cytology Prosencephalon - embryology Prosencephalon - growth & development Prosencephalon - metabolism Signal Transduction - physiology Stem Cells - cytology Stem Cells - metabolism Tretinoin - physiology |
title | Retinoic Acid Signaling Identifies a Distinct Precursor Population in the Developing and Adult Forebrain |
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