<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li C</submitter><funding>Deutsche Forschungsgemeinschaft</funding><funding>European Research Council</funding><funding>NIDDK NIH HHS</funding><funding>Chinese Scholarship Council. Deutsche Forschungsgemeinschaft</funding><funding>Prof. Martha Merrow and Dr. Francesca Sartor of the LMU generously provided access to and expertise regarding the Nikon Eclipse Ti2 microscope system</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><pagination>e06707</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12561471</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(40)</volume><pubmed_abstract>RNA-binding proteins regulate post-transcriptional gene translation, but the macrophage-specific role of Zc3h12c remains poorly characterized. Here, the role of Zc3h12c in macrophages is characterized using Tnfrsf11a&lt;sup>Cre&lt;/sup>-Zc3h12c&lt;sup>flox/flox&lt;/sup> mice. Both Tnfrsf11a and Zc3h12c are highly expressed in the kidney tissue from patients with chronic kidney disease and showed a positive association with an interstitial fibrosis score. Single cell RNA sequencing demonstrated abundant Tnfrsf11a expression in murine kidney macrophages and a correlation with the induction of chemokines, macrophage phagocytosis, and activation upon kidney injury. In various kidney injury models, Tnfrsf11a&lt;sup>Cre&lt;/sup>-Zc3h12c&lt;sup>flox/flox&lt;/sup> mice suffered from more injury and inflammation in the ki</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Macrophage Zc3h12c Limits Tissue Inflammation and Injury via Alternative Splicing of Pre-mRNA.</pubmed_title><pmcid>PMC12561471</pmcid><funding_grant_id>R01DK076077</funding_grant_id><funding_grant_id>INST 86/1851-1 FUGG</funding_grant_id><funding_grant_id>R01 DK087635</funding_grant_id><funding_grant_id>SFB TRR332</funding_grant_id><funding_grant_id>R01 DK076077</funding_grant_id><funding_grant_id>R01 DK105821</funding_grant_id><funding_grant_id>R01DK105821</funding_grant_id><funding_grant_id>R01DK087635</funding_grant_id><funding_grant_id>648274</funding_grant_id><funding_grant_id>GZ:INST 86/1851-1 FUGG</funding_grant_id><funding_grant_id>AN372/30-1</funding_grant_id><funding_grant_id>TRR332</funding_grant_id><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Zhu Z</pubmed_authors><pubmed_authors>Lech M</pubmed_authors><pubmed_authors>Susztak K</pubmed_authors><pubmed_authors>Schulz C</pubmed_authors><pubmed_authors>Zhang N</pubmed_authors><pubmed_authors>Kusunoki Y</pubmed_authors><pubmed_authors>Marschner JA</pubmed_authors><pubmed_authors>Watanabe-Kusunoki K</pubmed_authors><pubmed_authors>Zhao Z</pubmed_authors><pubmed_authors>Deng H</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Anders HJ</pubmed_authors><pubmed_authors>Steiger S</pubmed_authors><pubmed_authors>Xu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Macrophage Zc3h12c Limits Tissue Inflammation and Injury via Alternative Splicing of Pre-mRNA.</name><description>RNA-binding proteins regulate post-transcriptional gene translation, but the macrophage-specific role of Zc3h12c remains poorly characterized. Here, the role of Zc3h12c in macrophages is characterized using Tnfrsf11a&lt;sup>Cre&lt;/sup>-Zc3h12c&lt;sup>flox/flox&lt;/sup> mice. Both Tnfrsf11a and Zc3h12c are highly expressed in the kidney tissue from patients with chronic kidney disease and showed a positive association with an interstitial fibrosis score. Single cell RNA sequencing demonstrated abundant Tnfrsf11a expression in murine kidney macrophages and a correlation with the induction of chemokines, macrophage phagocytosis, and activation upon kidney injury. In various kidney injury models, Tnfrsf11a&lt;sup>Cre&lt;/sup>-Zc3h12c&lt;sup>flox/flox&lt;/sup> mice suffered from more injury and inflammation in the ki</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-06-05T08:58:16.455Z</modification><creation>2026-05-15T03:07:54.636Z</creation></dates><accession>S-EPMC12561471</accession><cross_references><pubmed>40834429</pubmed><doi>10.1002/advs.202506707</doi></cross_references></HashMap>