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            <title xml:lang="en">Characterization of transgenic mouse lines for selectively targeting satellite glial cells and macrophages in dorsal root ganglia</title>
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                <forename type="first">Yasmine</forename>
                <surname>Rabah</surname>
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                <forename type="first">Bruna</forename>
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                <forename type="first">Elsie</forename>
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              <date type="whenModified">2024-04-22 10:26:04</date>
              <date type="whenReleased">2021-12-02 11:08:34</date>
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            <idno type="halRefHtml">&lt;i&gt;PLoS ONE&lt;/i&gt;, 2020, 15 (9), pp.e0229475. &lt;a target="_blank" href="https://dx.doi.org/10.1371/journal.pone.0229475"&gt;&amp;#x27E8;10.1371/journal.pone.0229475&amp;#x27E9;&lt;/a&gt;</idno>
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            <idno type="stamp" n="UNIV-PARIS">Université Paris Cité</idno>
            <idno type="stamp" n="UNIVERSITE-PARIS" corresp="UNIV-PARIS">Université Paris Cité</idno>
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                <title xml:lang="en">Characterization of transgenic mouse lines for selectively targeting satellite glial cells and macrophages in dorsal root ganglia</title>
                <author role="aut">
                  <persName>
                    <forename type="first">Yasmine</forename>
                    <surname>Rabah</surname>
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                <author role="aut">
                  <persName>
                    <forename type="first">Bruna</forename>
                    <surname>Rubino</surname>
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                  <persName>
                    <forename type="first">Elsie</forename>
                    <surname>Moukarzel</surname>
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                  <idno type="halauthorid">2106007-0</idno>
                  <affiliation ref="#struct-1004691"/>
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                <author role="aut">
                  <persName>
                    <forename type="first">Cendra</forename>
                    <surname>Agulhon</surname>
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                <title level="j">PLoS ONE</title>
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                  <publisher>Public Library of Science</publisher>
                  <biblScope unit="volume">15</biblScope>
                  <biblScope unit="issue">9</biblScope>
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                  <date type="datePub">2020</date>
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              <p>The importance of glial cells in the modulation of neuronal processes is now generally accepted. In particular, enormous progress in our understanding of astrocytes and microglia physiology in the central nervous system (CNS) has been made in recent years, due to the development of genetic and molecular toolkits. However, the roles of satellite glial cells (SGCs) and macrophages-the peripheral counterparts of astrocytes and microglia-remain poorly studied despite their involvement in debilitating conditions, such as pain. Here, we characterized in dorsal root ganglia (DRGs), different genetically-modified mouse lines previously used for studying astrocytes and microglia, with the goal to implement them for investigating DRG SGC and macrophage functions. Although SGCs and astrocytes share some molecular properties, most tested transgenic lines were found to not be suitable for studying selectively a large number of SGCs within DRGs. Nevertheless, we identified and validated two mouse lines: (i) a CreERT2 recombinase-based mouse line allowing transgene expression almost exclusively in SGCs and in the vast majority of SGCs, and (ii) a GFP-expressing line allowing the selective visualization of macrophages. In conclusion, among the tools available for exploring astrocyte functions, a few can be used for studying selectively a great proportion of SGCs. Thus, efforts remain to be made to characterize other available mouse lines as well as to develop, rigorously characterize and validate new molecular tools to investigate the roles of DRG SGCs, but also macrophages, in health and disease.</p>
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          <date type="start">2020-01-01</date>
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