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The <jats:styled-content style=\"fixed-case\">PDL<\/jats:styled-content> is unique as it is the only ligament with both innervation and vascularization. Maxillary molars in 6\u2010week\u2010old male C57<jats:styled-content style=\"fixed-case\">BL<\/jats:styled-content>\/6 mice (N\u00a0=\u00a05) were experimentally translated for 2\u00a0weeks using an elastic spacer. Contralateral teeth were used as controls. Mechanical testing of the periodontal complex of a mouse in situ and imaging using X\u2010ray micro\u2010computed tomography (micro\u2010<jats:styled-content style=\"fixed-case\">XCT<\/jats:styled-content>) illustrated deformations within blood vessels (<jats:styled-content style=\"fixed-case\">BV<\/jats:styled-content>) of the <jats:styled-content style=\"fixed-case\">PDL<\/jats:styled-content>. <jats:styled-content style=\"fixed-case\">PDL<\/jats:styled-content>\u2010bone and <jats:styled-content style=\"fixed-case\">PDL<\/jats:styled-content>\u2010cementum entheses at the widened and narrowed <jats:styled-content style=\"fixed-case\">PDL<\/jats:styled-content>\u2010spaces following experimental tooth movement (<jats:styled-content style=\"fixed-case\">ETM<\/jats:styled-content>) illustrated osterix (<jats:styled-content style=\"fixed-case\">OSX<\/jats:styled-content>), bone sialoprotein (<jats:styled-content style=\"fixed-case\">BSP<\/jats:styled-content>), cluster of differentiation 146 (<jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>146), and protein gene product 9.5 (<jats:styled-content style=\"fixed-case\">PGP<\/jats:styled-content>9.5), indicating active remodeling at these sites. <jats:styled-content style=\"fixed-case\">PGP<\/jats:styled-content>9.5 positive nerve bundles (<jats:styled-content style=\"fixed-case\">NB<\/jats:styled-content>s) were co\u2010localized with multinucleated cells (<jats:styled-content style=\"fixed-case\">MC<\/jats:styled-content>s), Howship's resorption lacunae, and <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>146 positive <jats:styled-content style=\"fixed-case\">BV<\/jats:styled-content>s. Association between nerves and <jats:styled-content style=\"fixed-case\">MC<\/jats:styled-content> was complemented by visualizing the proximity of osmium tetroxide stained <jats:styled-content style=\"fixed-case\">NB<\/jats:styled-content>s with the ultrastructure of <jats:styled-content style=\"fixed-case\">MC<\/jats:styled-content>s by performing scanning transmission electron microscopy. Spatial association of <jats:styled-content style=\"fixed-case\">NB<\/jats:styled-content> with <jats:styled-content style=\"fixed-case\">BV<\/jats:styled-content>, and <jats:styled-content style=\"fixed-case\">NB<\/jats:styled-content> with <jats:styled-content style=\"fixed-case\">MC<\/jats:styled-content>, provided insights into the plausible co\u2010activation of <jats:styled-content style=\"fixed-case\">NB<\/jats:styled-content>s to initiate osteoclastic activity. Resorption of mineral occurred as an attempt to restore <jats:styled-content style=\"fixed-case\">PDL<\/jats:styled-content>\u2010space of the load\u2010bearing complex, specifically at the <jats:styled-content style=\"fixed-case\">PDL<\/jats:styled-content>\u2010entheses. Mapping of anatomy\u2010specific structural elements and their association with regenerative molecules by correlating light and electron micrographs provided insights into the use of these extracellular matrix molecules as plausible targets for pharmacological interventions related to tooth movement. Within the realm of tissue regeneration, modulation of load can reverse naturally occurring mineral formation to experimentally induced resorption, and naturally occurring mineral resorption to experimentally induced formation at the enthesial sites to permit tooth translation.<\/jats:p>","DOI":"10.1111\/jre.12625","type":"journal-article","created":{"date-parts":[[2018,11,28]],"date-time":"2018-11-28T19:03:30Z","timestamp":1543431810000},"page":"251-258","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":13,"title":["Microanatomical changes and biomolecular expression at the <scp>PDL<\/scp>\u2010entheses during experimental tooth movement"],"prefix":"10.1111","volume":"54","author":[{"given":"Lynn","family":"Yang","sequence":"first","affiliation":[{"name":"Division of Biomaterials and Bioengineering Department of Preventive and Restorative Dental Sciences University of California  San Francisco 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