<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>102(4)</volume><submitter>Supatto W</submitter><pubmed_abstract>The complex biomechanical events associated with embryo development are investigated in vivo, by using femtosecond laser pulse-induced ablation combined with multimodal nonlinear microscopy. We demonstrate controlled intravital ablations preserving local cytoskeleton dynamics and resulting in the modulation of specific morphogenetic movements in nonmutant Drosophila embryos. A quantitative description of complex movements is obtained both in GFP-expressing systems by using whole-embryo two-photon microscopy and in unlabeled nontransgenic embryos by using third harmonic generation microscopy. This methodology provides insight into the issue of mechano-sensitive gene expression by revealing the correlation of in vivo tissue deformation patterns with Twist protein expression in stomodeal cells at gastrulation.</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pagination>1047-52</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC545833</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>In vivo modulation of morphogenetic movements in Drosophila embryos with femtosecond laser pulses.</pubmed_title><pmcid>PMC545833</pmcid><pubmed_authors>Supatto W</pubmed_authors><pubmed_authors>Debarre D</pubmed_authors><pubmed_authors>Beaurepaire E</pubmed_authors><pubmed_authors>Moulia B</pubmed_authors><pubmed_authors>Brouzes E</pubmed_authors><pubmed_authors>Farge E</pubmed_authors><pubmed_authors>Martin JL</pubmed_authors></additional><is_claimable>false</is_claimable><name>In vivo modulation of morphogenetic movements in Drosophila embryos with femtosecond laser pulses.</name><description>The complex biomechanical events associated with embryo development are investigated in vivo, by using femtosecond laser pulse-induced ablation combined with multimodal nonlinear microscopy. We demonstrate controlled intravital ablations preserving local cytoskeleton dynamics and resulting in the modulation of specific morphogenetic movements in nonmutant Drosophila embryos. A quantitative description of complex movements is obtained both in GFP-expressing systems by using whole-embryo two-photon microscopy and in unlabeled nontransgenic embryos by using third harmonic generation microscopy. This methodology provides insight into the issue of mechano-sensitive gene expression by revealing the correlation of in vivo tissue deformation patterns with Twist protein expression in stomodeal cells at gastrulation.</description><dates><release>2005-01-01T00:00:00Z</release><publication>2005 Jan</publication><modification>2025-04-20T01:38:36.737Z</modification><creation>2019-03-27T01:08:32Z</creation></dates><accession>S-EPMC545833</accession><cross_references><pubmed>15657140</pubmed><doi>10.1073/pnas.0405316102</doi></cross_references></HashMap>