<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sharifi KA</submitter><funding>NCI NIH HHS</funding><funding>NINDS NIH HHS</funding><pagination>1353142</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10915230</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18</volume><pubmed_abstract>The Wnt pathway plays critical roles in neurogenesis. The expression of &lt;i>Axin2&lt;/i> is induced by Wnt/β-catenin signaling, making this gene a reliable indicator of canonical Wnt activity. We employed pulse-chase genetic lineage tracing with the &lt;i>Axin2-CreERT2&lt;/i> allele to follow the fate of &lt;i>Axin2&lt;/i>+ lineage in the adult hippocampal formation. We found &lt;i>Axin2&lt;/i> expressed in astrocytes, neurons and endothelial cells, as well as in the choroid plexus epithelia. Simultaneously with the induction of &lt;i>Axin2&lt;/i> fate mapping by tamoxifen, we marked the dividing cells with 5-ethynyl-2'-deoxyuridine (EdU). Tamoxifen induction led to a significant increase in labeled dentate gyrus granule cells three months later. However, none of these neurons showed any EdU signal. Conversely, six months after the pulse-chase labeling with tamoxifen/EdU, we identified granule neurons that were positive for both EdU and tdTomato lineage tracer in each animal. Our data indicates that &lt;i>Axin2&lt;/i> is expressed at multiple stages of adult granule neuron differentiation. Furthermore, these findings suggest that the integration process of adult-born neurons from specific cell lineages may require more time than previously thought.</pubmed_abstract><journal>Frontiers in neuroscience</journal><pubmed_title>Exploring the dynamics of adult &lt;i>Axin2&lt;/i> cell lineage integration into dentate gyrus granule neurons.</pubmed_title><pmcid>PMC10915230</pmcid><funding_grant_id>R01 CA279134</funding_grant_id><funding_grant_id>R21 NS116431</funding_grant_id><pubmed_authors>Soldozy S</pubmed_authors><pubmed_authors>DeWitt MR</pubmed_authors><pubmed_authors>Farzad F</pubmed_authors><pubmed_authors>Kalani MYS</pubmed_authors><pubmed_authors>Sheehan J</pubmed_authors><pubmed_authors>Tvrdik P</pubmed_authors><pubmed_authors>Price RJ</pubmed_authors><pubmed_authors>Sharifi KA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Exploring the dynamics of adult &lt;i>Axin2&lt;/i> cell lineage integration into dentate gyrus granule neurons.</name><description>The Wnt pathway plays critical roles in neurogenesis. The expression of &lt;i>Axin2&lt;/i> is induced by Wnt/β-catenin signaling, making this gene a reliable indicator of canonical Wnt activity. We employed pulse-chase genetic lineage tracing with the &lt;i>Axin2-CreERT2&lt;/i> allele to follow the fate of &lt;i>Axin2&lt;/i>+ lineage in the adult hippocampal formation. We found &lt;i>Axin2&lt;/i> expressed in astrocytes, neurons and endothelial cells, as well as in the choroid plexus epithelia. Simultaneously with the induction of &lt;i>Axin2&lt;/i> fate mapping by tamoxifen, we marked the dividing cells with 5-ethynyl-2'-deoxyuridine (EdU). Tamoxifen induction led to a significant increase in labeled dentate gyrus granule cells three months later. However, none of these neurons showed any EdU signal. Conversely, six months after the pulse-chase labeling with tamoxifen/EdU, we identified granule neurons that were positive for both EdU and tdTomato lineage tracer in each animal. Our data indicates that &lt;i>Axin2&lt;/i> is expressed at multiple stages of adult granule neuron differentiation. Furthermore, these findings suggest that the integration process of adult-born neurons from specific cell lineages may require more time than previously thought.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2025-04-19T09:59:50.837Z</modification><creation>2025-04-19T09:59:50.837Z</creation></dates><accession>S-EPMC10915230</accession><cross_references><pubmed>38449734</pubmed><doi>10.3389/fnins.2024.1353142</doi></cross_references></HashMap>