<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rajagopalan KS</submitter><funding>NIDDK NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>Regenerative Medicine Minnesota</funding><funding>NIH</funding><pagination>1803</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9180447</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(11)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Scattered tubular-like cells (STCs) are dedifferentiated renal tubular cells endowed with progenitor-like characteristics to repair injured parenchymal cells. STCs may be damaged and rendered ineffective by renal artery stenosis (RAS), but the underlying processes remain unclear. We hypothesized that RAS alters the epigenetic landscape on DNA and the ensuing gene transcriptional profile of swine STCs.&lt;h4>Methods&lt;/h4>CD24+/CD133+ STCs were isolated from pig kidneys after 10 weeks of RAS or sham (&lt;i>n&lt;/i> = 3 each) and their whole 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC) profiles were examined by 5mC and 5hmC immunoprecipitation sequencing (MeDIP-/hMeDIP-seq, respectively). A subsequent integrated (MeDIP/hMeDIP-seq/mRNA-seq) analysis was performed by compa</pubmed_abstract><journal>Cells</journal><pubmed_title>Renal Ischemia Induces Epigenetic Changes in Apoptotic, Proteolytic, and Mitochondrial Genes in Swine Scattered Tubular-like Cells.</pubmed_title><pmcid>PMC9180447</pmcid><funding_grant_id>HL095638</funding_grant_id><funding_grant_id>DK129240</funding_grant_id><funding_grant_id>RMM 091620 DS 004</funding_grant_id><funding_grant_id>R01 DK122734</funding_grant_id><funding_grant_id>R01 DK129240</funding_grant_id><funding_grant_id>R56 DK129240</funding_grant_id><funding_grant_id>K08 DK118120</funding_grant_id><funding_grant_id>R21 DK118391</funding_grant_id><funding_grant_id>DK118120</funding_grant_id><funding_grant_id>R01 DK128017</funding_grant_id><funding_grant_id>DK122734</funding_grant_id><funding_grant_id>R01 HL095638</funding_grant_id><funding_grant_id>DK118391</funding_grant_id><pubmed_authors>Herrmann SM</pubmed_authors><pubmed_authors>Glasstetter LM</pubmed_authors><pubmed_authors>Jordan KL</pubmed_authors><pubmed_authors>Irazabal MV</pubmed_authors><pubmed_authors>Saadiq IM</pubmed_authors><pubmed_authors>Lerman LO</pubmed_authors><pubmed_authors>Eirin A</pubmed_authors><pubmed_authors>Chade AR</pubmed_authors><pubmed_authors>Zhu XY</pubmed_authors><pubmed_authors>Thaler R</pubmed_authors><pubmed_authors>Rajagopalan KS</pubmed_authors><pubmed_authors>Tang H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Renal Ischemia Induces Epigenetic Changes in Apoptotic, Proteolytic, and Mitochondrial Genes in Swine Scattered Tubular-like Cells.</name><description>&lt;h4>Background&lt;/h4>Scattered tubular-like cells (STCs) are dedifferentiated renal tubular cells endowed with progenitor-like characteristics to repair injured parenchymal cells. STCs may be damaged and rendered ineffective by renal artery stenosis (RAS), but the underlying processes remain unclear. We hypothesized that RAS alters the epigenetic landscape on DNA and the ensuing gene transcriptional profile of swine STCs.&lt;h4>Methods&lt;/h4>CD24+/CD133+ STCs were isolated from pig kidneys after 10 weeks of RAS or sham (&lt;i>n&lt;/i> = 3 each) and their whole 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC) profiles were examined by 5mC and 5hmC immunoprecipitation sequencing (MeDIP-/hMeDIP-seq, respectively). A subsequent integrated (MeDIP/hMeDIP-seq/mRNA-seq) analysis was performed by compa</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2026-04-08T10:02:22.452Z</modification><creation>2025-04-05T19:55:53.313Z</creation></dates><accession>S-EPMC9180447</accession><cross_references><pubmed>35681498</pubmed><doi>10.3390/cells11111803</doi></cross_references></HashMap>