<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Tsissios G</submitter><funding>NEI NIH HHS</funding><funding>NINDS NIH HHS</funding><pubmed_abstract>Previous studies indicated that macrophages play a role during lens regeneration in newts, but their function has not been tested experimentally. Here we generated a transgenic newt reporter line in which macrophages can be visualized &lt;i>in vivo&lt;/i>. Using this new tool, we analyzed the location of macrophages during lens regeneration. We uncovered early gene expression changes using bulk RNAseq in two newt species, &lt;i>Notophthalmus viridescens&lt;/i> and &lt;i>Pleurodeles waltl&lt;/i>. Next, we used clodronate liposomes to deplete macrophages, which inhibited lens regeneration in both newt species. Macrophage depletion induced the formation of scar-like tissue, an increased and sustained inflammatory response, an early decrease in iris pigment epithelial cell (iPEC) proliferation and a late increa</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2023.06.04.543633</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10274724</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Macrophages modulate fibrosis during newt lens regeneration.</pubmed_title><pmcid>PMC10274724</pmcid><funding_grant_id>R21 EY031865</funding_grant_id><funding_grant_id>R01 EY027801</funding_grant_id><funding_grant_id>R21 EY033916</funding_grant_id><funding_grant_id>F99 NS129167</funding_grant_id><pubmed_authors>Tangeman JA</pubmed_authors><pubmed_authors>Araus AJ</pubmed_authors><pubmed_authors>Ratvasky SC</pubmed_authors><pubmed_authors>Grajales-Esquivel E</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Yun MH</pubmed_authors><pubmed_authors>Simon A</pubmed_authors><pubmed_authors>Tsissios G</pubmed_authors><pubmed_authors>Perez-Estrada JR</pubmed_authors><pubmed_authors>Rio-Tsonis KD</pubmed_authors><pubmed_authors>Chen W</pubmed_authors><pubmed_authors>Sallese A</pubmed_authors><pubmed_authors>Martinez A</pubmed_authors><pubmed_authors>Visser KJ</pubmed_authors><pubmed_authors>Smucker B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Macrophages modulate fibrosis during newt lens regeneration.</name><description>Previous studies indicated that macrophages play a role during lens regeneration in newts, but their function has not been tested experimentally. Here we generated a transgenic newt reporter line in which macrophages can be visualized &lt;i>in vivo&lt;/i>. Using this new tool, we analyzed the location of macrophages during lens regeneration. We uncovered early gene expression changes using bulk RNAseq in two newt species, &lt;i>Notophthalmus viridescens&lt;/i> and &lt;i>Pleurodeles waltl&lt;/i>. Next, we used clodronate liposomes to deplete macrophages, which inhibited lens regeneration in both newt species. Macrophage depletion induced the formation of scar-like tissue, an increased and sustained inflammatory response, an early decrease in iris pigment epithelial cell (iPEC) proliferation and a late increa</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jun</publication><modification>2025-04-18T19:23:08.803Z</modification><creation>2025-04-07T07:07:37.487Z</creation></dates><accession>S-EPMC10274724</accession><cross_references><pubmed>37333184</pubmed><doi>10.1101/2023.06.04.543633</doi></cross_references></HashMap>