<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Latzko L</submitter><funding>Tiroler Wissenschaftsförderung</funding><pagination>134-143</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12779247</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(1)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>The NLRP3 inflammasome is a damage sensor driving pyroptotic cell death during orthodontic tooth movement (OTM). Recent studies have revealed impaired one-week OTM in mice lacking NLRP3. However, the relevance of NLRP3 during long-term OTM remains unknown.&lt;h4>Materials and methods&lt;/h4>OTM was analysed after 7, 14 and 21 days of force application in mice lacking NLRP3 (NLRP3&lt;sup>-/-&lt;/sup>), wild-type (WT) male and female littermates. Micro-computed tomography (μCT) was used to assess molar movement and bone quality. Tartrate-resistant acid phosphatase (TRAP) staining was used to visualise osteoclastic activity.&lt;h4>Results&lt;/h4>We show here that after 2 weeks of force application, OTM was delayed in mice lacking NLRP3 compared to WT mice. Interestingly, OTM regained speed in</pubmed_abstract><journal>Orthodontics &amp; craniofacial research</journal><pubmed_title>The NLRP3 Inflammasome Regulates Orthodontic Tooth Movement.</pubmed_title><pmcid>PMC12779247</pmcid><funding_grant_id>F.45069/8-2022</funding_grant_id><funding_grant_id>F.45069/8‐2022</funding_grant_id><pubmed_authors>Gruber R</pubmed_authors><pubmed_authors>Hayback J</pubmed_authors><pubmed_authors>Manzl C</pubmed_authors><pubmed_authors>Latzko L</pubmed_authors><pubmed_authors>Degenhart G</pubmed_authors><pubmed_authors>Crismani AG</pubmed_authors><pubmed_authors>Blumer MJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>The NLRP3 Inflammasome Regulates Orthodontic Tooth Movement.</name><description>&lt;h4>Objective&lt;/h4>The NLRP3 inflammasome is a damage sensor driving pyroptotic cell death during orthodontic tooth movement (OTM). Recent studies have revealed impaired one-week OTM in mice lacking NLRP3. However, the relevance of NLRP3 during long-term OTM remains unknown.&lt;h4>Materials and methods&lt;/h4>OTM was analysed after 7, 14 and 21 days of force application in mice lacking NLRP3 (NLRP3&lt;sup>-/-&lt;/sup>), wild-type (WT) male and female littermates. Micro-computed tomography (μCT) was used to assess molar movement and bone quality. Tartrate-resistant acid phosphatase (TRAP) staining was used to visualise osteoclastic activity.&lt;h4>Results&lt;/h4>We show here that after 2 weeks of force application, OTM was delayed in mice lacking NLRP3 compared to WT mice. Interestingly, OTM regained speed in</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-06-06T11:30:55.967Z</modification><creation>2026-05-29T03:12:53.976Z</creation></dates><accession>S-EPMC12779247</accession><cross_references><pubmed>41221981</pubmed><doi>10.1111/ocr.70059</doi></cross_references></HashMap>