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Here, we first compared layer thickness of the olfactory bulb between wild\u2010type (<jats:styled-content style=\"fixed-case\">WT<\/jats:styled-content>) and <jats:italic><jats:styled-content style=\"fixed-case\">CRMP<\/jats:styled-content>4<\/jats:italic>\u2010knockout (<jats:styled-content style=\"fixed-case\">KO<\/jats:styled-content>) mice. The mitral cell layer (<jats:styled-content style=\"fixed-case\">MCL<\/jats:styled-content>) was significantly thinner, whereas the external plexiform layer (<jats:styled-content style=\"fixed-case\">EPL<\/jats:styled-content>) was significantly thicker in <jats:italic><jats:styled-content style=\"fixed-case\">CRMP<\/jats:styled-content>4<\/jats:italic>\u2010<jats:styled-content style=\"fixed-case\">KO<\/jats:styled-content> mice at postnatal day 0 (<jats:styled-content style=\"fixed-case\">PD<\/jats:styled-content>0) compared with <jats:styled-content style=\"fixed-case\">WT<\/jats:styled-content>s. However, differences in layer thickness disappeared by <jats:styled-content style=\"fixed-case\">PD<\/jats:styled-content>14. No apoptotic cells were found in the <jats:styled-content style=\"fixed-case\">MCL<\/jats:styled-content>, and the number of mitral cells (<jats:styled-content style=\"fixed-case\">MC<\/jats:styled-content>s) identified with a specific marker (i.e. Tbx21 antibody) did not change in <jats:italic><jats:styled-content style=\"fixed-case\">CRMP<\/jats:styled-content>4<\/jats:italic>\u2010<jats:styled-content style=\"fixed-case\">KO<\/jats:styled-content> neonates. However, DiI\u2010tracing showed that the length of mitral cell apical dendrites was greater in <jats:italic><jats:styled-content style=\"fixed-case\">CRMP<\/jats:styled-content>4<\/jats:italic>\u2010<jats:styled-content style=\"fixed-case\">KO<\/jats:styled-content> neonates than in <jats:styled-content style=\"fixed-case\">WT<\/jats:styled-content>s. In addition, expression of <jats:styled-content style=\"fixed-case\">CRMP<\/jats:styled-content>4 <jats:styled-content style=\"fixed-case\">mRNA<\/jats:styled-content> in <jats:styled-content style=\"fixed-case\">WT<\/jats:styled-content> mice was most abundant in the <jats:styled-content style=\"fixed-case\">MCL<\/jats:styled-content> at <jats:styled-content style=\"fixed-case\">PD<\/jats:styled-content>0 and decreased afterward. These results suggest that <jats:styled-content style=\"fixed-case\">CRMP<\/jats:styled-content>4 contributes to dendritic elongation. Our <jats:italic>in\u00a0vitro<\/jats:italic> studies showed that deletion or knockdown of <jats:italic><jats:styled-content style=\"fixed-case\">CRMP<\/jats:styled-content>4<\/jats:italic> resulted in enhanced growth of <jats:styled-content style=\"fixed-case\">MAP<\/jats:styled-content>2\u2010positive neurites, whereas overexpression of <jats:italic><jats:styled-content style=\"fixed-case\">CRMP<\/jats:styled-content>4<\/jats:italic> reduced their growth, suggesting a new role for <jats:styled-content style=\"fixed-case\">CRMP<\/jats:styled-content>4 as a suppressor of dendritic elongation. Overall, our data suggest that disruption of <jats:styled-content style=\"fixed-case\">CRMP<\/jats:styled-content>4 produces a temporary alteration in <jats:styled-content style=\"fixed-case\">EPL<\/jats:styled-content> thickness, which is constituted mainly of mitral cell apical dendrites, through the enhanced growth of these dendrites.<\/jats:p>","DOI":"10.1111\/joa.12434","type":"journal-article","created":{"date-parts":[[2016,1,7]],"date-time":"2016-01-07T12:19:34Z","timestamp":1452169174000},"page":"792-804","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":13,"title":["Deletion of collapsin response mediator protein 4 results in abnormal layer thickness and elongation of mitral cell apical dendrites in the neonatal olfactory bulb"],"prefix":"10.1111","volume":"228","author":[{"given":"Atsuhiro","family":"Tsutiya","sequence":"first","affiliation":[{"name":"Graduate School of Life Sciences Toyo University Oura Gunma 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