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        <title>Microglia and CD206+ border-associated mouse macrophages maintain their embryonic origin during Alzheimer&rsquo;s disease</title>
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        <h1>Microglia and CD206+ border-associated mouse macrophages maintain their embryonic origin during Alzheimer&rsquo;s disease&nbsp;(doi:10.21979/N9/9RCHLK)</h1>
        <table border="0" cellpadding="5" cellspacing="0">
            <tr>
                <td valign="top">
                    <p>
                        <b>View:</b>
                    </p>
                </td><td>
                    <p>
                        <a href="#1.0">Part 1: Document Description</a>
                        <br>
                        <a href="#2.0">Part 2: Study Description</a>
                        <br>
                        <a href="#5.0">Part 5: Other
                                        Study-Related Materials</a>
                        <br>
                        <a href="">Entire Codebook</a>
                    </p>
                </td>
            </tr>
        </table>
        <table border="0" cellpadding="5" cellspacing="5">
            <tr class="h1">
                <th align="left" colspan="2">
                    <p>
                        <a name="1.0" id="1.0">Document Description</a>
                    </p>
                </th>
            </tr>
            <tr class="h2">
                <th colspan="2">
                    <p>Citation</p>
                </th>
            </tr>
            <tr>
                <td class="h3">
                    <p>Title:</p>
                </td><td>
                    <p>Microglia and CD206+ border-associated mouse macrophages maintain their embryonic origin during Alzheimer&rsquo;s disease</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Identification Number:</p>
                </td><td>
                    <p>doi:10.21979/N9/9RCHLK</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Distributor:</p>
                </td><td>
                    <p>DR-NTU (Data)</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Date of Distribution:</p>
                </td><td>
                    <p>2021-10-06</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Version:</p>
                </td><td>
                    <p>1</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Bibliographic Citation:</p>
                </td><td>
                    <p>Wu, Xiaoting; Saito, Takashi; Saido, Takaomi C.; Barron, Anna M; Ruedl, Christiane, 2021, "Microglia and CD206+ border-associated mouse macrophages maintain their embryonic origin during Alzheimer&rsquo;s disease", https://doi.org/10.21979/N9/9RCHLK, DR-NTU (Data), V1</p>
                </td>
            </tr>
            <tr class="h1">
                <th colspan="2">
                    <p>
                        <a name="2.0">Study Description</a>
                    </p>
                </th>
            </tr>
            <tr class="h2">
                <th colspan="2">
                    <p>Citation</p>
                </th>
            </tr>
            <tr>
                <td class="h3">
                    <p>Title:</p>
                </td><td>
                    <p>Microglia and CD206+ border-associated mouse macrophages maintain their embryonic origin during Alzheimer&rsquo;s disease</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Identification Number:</p>
                </td><td>
                    <p>doi:10.21979/N9/9RCHLK</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Authoring Entity:</p>
                </td><td>
                    <p>Wu, Xiaoting (Nanyang Technological University)</p>
                </td>
            </tr>
            <tr>
                <td class="h3"></td><td>
                    <p>Saito, Takashi (Laboratory for Proteolytic Neuroscience, Riken Center for Brain Science, Wako, Japan)</p>
                </td>
            </tr>
            <tr>
                <td class="h3"></td><td>
                    <p>Saido, Takaomi C. (Laboratory for Proteolytic Neuroscience, Riken Center for Brain Science, Wako, Japan)</p>
                </td>
            </tr>
            <tr>
                <td class="h3"></td><td>
                    <p>Barron, Anna M (Nanyang Technological University)</p>
                </td>
            </tr>
            <tr>
                <td class="h3"></td><td>
                    <p>Ruedl, Christiane (Nanyang Technological University)</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Software used in Production:</p>
                </td><td>
                    <p>Flowjo</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Grant Number:</p>
                </td><td>
                    <p>MOE AcRF Tier 1</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Distributor:</p>
                </td><td>
                    <p>DR-NTU (Data)</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Access Authority:</p>
                </td><td>
                    <p>Ruedl, Christiane</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Depositor:</p>
                </td><td>
                    <p>Ruedl, Christiane</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Date of Deposit:</p>
                </td><td>
                    <p>2021-07-26</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Holdings Information:</p>
                </td><td>
                    <p>https://doi.org/10.21979/N9/9RCHLK</p>
                </td>
            </tr>
            <tr class="h2">
                <th colspan="2">
                    <p>Study Scope</p>
                </th>
            </tr>
            <tr>
                <td class="h3">
                    <p>Keywords:</p>
                </td><td>
                    <p>Medicine, Health and Life Sciences, Medicine, Health and Life Sciences, Inducible fate-mapping analysis demonstrates that neither microglia, disease-associated microglia nor border-associated macrophages are replenished by bone marrow-derived cells in Alzheimer&rsquo;s disease.</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Abstract:</p>
                </td><td>
                    <p>Brain microglia and border-associated macrophages (BAMs) display distinct spatial, developmental, and phenotypic features. Although at steady-state, the origins of distinct brain macrophages are well-documented, the dynamics of their replenishment in neurodegenerative disorders remain elusive, particularly for activated CD11c+ microglia and BAMs. In this study, we conducted a comprehensive fate-mapping analysis of murine microglia and BAMs and their turnover kinetics during Alzheimer&rsquo;s disease (AD) progression. We used a novel inducible AD mouse model to investigate the contribution of bone marrow cells to the pool of foetal-derived brain macrophages during the development of AD. We demonstrated that microglia remain a remarkably stable embryonic-derived population even during the progression of AD pathology, indicating that neither parenchymal macrophage subpopulation originates from, nor are replenished by, bone marrow (BM)-derived cells. At the border-associated brain regions, bona fide CD206+ BAMs are minimally replaced by BM-derived cells, and their turnover rates are not accelerated by AD. In contrast, all other myeloid cells are swiftly replenished by BM progenitors. This information further elucidates the turnover kinetics of these cells not only at steady-state, but also in neurodegenerative diseases, which is crucial for identifying potential novel therapeutic targets.</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Kind of Data:</p>
                </td><td>
                    <p>Experimental raw data</p>
                </td>
            </tr>
            <tr class="h2">
                <th colspan="2">
                    <p>Methodology and Processing</p>
                </th>
            </tr>
            <tr>
                <th colspan="2">
                    <p>Sources Statement</p>
                </th>
            </tr>
            <tr class="h2">
                <th colspan="2">
                    <p>Data Access</p>
                </th>
            </tr>
            <tr class="h2">
                <th colspan="2">
                    <p>Other Study Description Materials</p>
                </th>
            </tr>
            <tr>
                <th colspan="2">
                    <p>Related Publications</p>
                </th>
            </tr>
            <tr class="h2">
                <th colspan="2">
                    <p>Citation</p>
                </th>
            </tr>
            <tr>
                <td class="h3">
                    <p>Identification Number:</p>
                </td><td>
                    <p>10.7554/eLife.71879</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Bibliographic Citation:</p>
                </td><td>
                    <p>Wu, X., Saito, T., Saido, T. C., Barron, A. M., &amp; Ruedl, C. (2021). Microglia and CD206+ border-associated mouse macrophages maintain their embryonic origin during Alzheimer's disease. eLife, 10, e71879.</p>
                </td>
            </tr>
            (<a href="https://elifesciences.org/articles/71879">external link</a>)


            <tr class="h2">
                <th colspan="2">
                    <p>Citation</p>
                </th>
            </tr>
            <tr>
                <td class="h3">
                    <p>Identification Number:</p>
                </td><td>
                    <p>10356/159385</p>
                </td>
            </tr>
            <tr>
                <td class="h3">
                    <p>Bibliographic Citation:</p>
                </td><td>
                    <p>Wu, X., Saito, T., Saido, T. C., Barron, A. M. &amp; Ruedl, C. (2021). Microglia and CD206⁺ border-associated mouse macrophages maintain their embryonic origin during Alzheimer's disease. ELife, 10, e71879-.</p>
                </td>
            </tr>
            (<a href="https://hdl.handle.net/10356/159385">external link</a>)


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                        <a name="f75028"></a><a name="5.0">Other Study-Related Materials</a>
                    </p>
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                <td align="right" valign="top">
                    <p>Label:</p>
                </td><td>
                    <p>Fig.1_figure supplement 1.zip</p>
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                <td class="h3">
                    <p>Notes:</p>
                </td><td>
                    <p>application/zip</p>
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                    <p>Fig.1_figure supplement 2.zip</p>
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                    <p>application/zip</p>
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                    <p>Fig.1.zip</p>
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                    <p>Fig.2 _figure supplement 1.zip</p>
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                    <p>application/zip</p>
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                        <a name="f75024"></a><a name="5.0">Other Study-Related Materials</a>
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                    <p>Fig.2.zip</p>
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                </td><td>
                    <p>application/zip</p>
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                    <p>
                        <a name="f75031"></a><a name="5.0">Other Study-Related Materials</a>
                    </p>
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                    <p>Fig.3.zip</p>
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                </td><td>
                    <p>application/zip</p>
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                    <p>
                        <a name="f75029"></a><a name="5.0">Other Study-Related Materials</a>
                    </p>
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                    <p>Label:</p>
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                    <p>Fig.4_figure supplement 2.zip</p>
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                    <p>application/zip</p>
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                        <a name="f75026"></a><a name="5.0">Other Study-Related Materials</a>
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                    <p>Fig.4.zip</p>
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