<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>28(2)</volume><submitter>Ju-Rong Y</submitter><pubmed_abstract>Trichorhinophalangeal 1 (Trps1) is a transcription factor essential for epithelial cell morphogenesis during kidney development, but the role of Trps1 in AKI induced by ischemia-reperfusion (I/R) remains unclear. Our study investigated Trps1 expression during kidney repair after acute I/R in rats and explored the molecular mechanisms by which Trps1 promotes renal tubular epithelial cell proliferation. Trps1 expression positively associated with the extent of renal repair after I/R injury. Compared with wild-type rats, rats with knockdown of Trps1 exhibited significantly delayed renal repair in the moderate I/R model, with lower GFR levels and more severe morphologic injury, whereas rats overexpressing Trps1 exhibited significantly accelerated renal repair after severe I/R injury. Additiona</pubmed_abstract><journal>Journal of the American Society of Nephrology : JASN</journal><pagination>532-544</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5280010</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Transcription Factor Trps1 Promotes Tubular Cell Proliferation after Ischemia-Reperfusion Injury through cAMP-Specific 3',5'-Cyclic Phosphodiesterase 4D and AKT.</pubmed_title><pmcid>PMC5280010</pmcid><pubmed_authors>Li-Rong L</pubmed_authors><pubmed_authors>Kai-Long L</pubmed_authors><pubmed_authors>Ju-Rong Y</pubmed_authors><pubmed_authors>Ya-Ni H</pubmed_authors><pubmed_authors>Bi-Qiong F</pubmed_authors><pubmed_authors>Kun H</pubmed_authors><pubmed_authors>Ke-Hong C</pubmed_authors><pubmed_authors>Jian-Guo Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcription Factor Trps1 Promotes Tubular Cell Proliferation after Ischemia-Reperfusion Injury through cAMP-Specific 3',5'-Cyclic Phosphodiesterase 4D and AKT.</name><description>Trichorhinophalangeal 1 (Trps1) is a transcription factor essential for epithelial cell morphogenesis during kidney development, but the role of Trps1 in AKI induced by ischemia-reperfusion (I/R) remains unclear. Our study investigated Trps1 expression during kidney repair after acute I/R in rats and explored the molecular mechanisms by which Trps1 promotes renal tubular epithelial cell proliferation. Trps1 expression positively associated with the extent of renal repair after I/R injury. Compared with wild-type rats, rats with knockdown of Trps1 exhibited significantly delayed renal repair in the moderate I/R model, with lower GFR levels and more severe morphologic injury, whereas rats overexpressing Trps1 exhibited significantly accelerated renal repair after severe I/R injury. Additiona</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Feb</publication><modification>2026-05-29T22:27:22.249Z</modification><creation>2019-03-26T22:59:15Z</creation></dates><accession>S-EPMC5280010</accession><cross_references><pubmed>27466160</pubmed><doi>10.1681/asn.2016010009</doi><doi>10.1681/ASN.2016010009</doi></cross_references></HashMap>