{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,30]],"date-time":"2026-10-30T07:55:58Z","timestamp":1793346958322,"version":"4.5.0"},"reference-count":54,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"12","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JASN"],"published-print":{"date-parts":[[2018,12]]},"abstract":"\n Background<\/jats:title>\n \n The mammalian kidney develops through reciprocal inductive signals between the metanephric mesenchyme and ureteric bud. Transcription factor 21 (Tcf21) is highly expressed in the metanephric mesenchyme, including Six2-expressing cap mesenchyme and Foxd1-expressing stromal mesenchyme.\n Tcf21<\/jats:italic>\n knockout mice die in the perinatal period from severe renal hypodysplasia. In humans,\n Tcf21<\/jats:italic>\n mRNA levels are reduced in renal tissue from human fetuses with renal dysplasia. The molecular mechanisms underlying these renal defects are not yet known.\n <\/jats:p>\n <\/jats:sec>\n \n Methods<\/jats:title>\n \n Using a variety of techniques to assess kidney development and gene expression, we compared the phenotypes of wild-type mice, mice with germline deletion of the\n Tcf21<\/jats:italic>\n gene, mice with stromal mesenchyme\u2013specific\n Tcf21<\/jats:italic>\n deletion, and mice with cap mesenchyme\u2013specific\n Tcf21<\/jats:italic>\n deletion.\n <\/jats:p>\n <\/jats:sec>\n \n Results<\/jats:title>\n \n Germline deletion of\n Tcf21<\/jats:italic>\n leads to impaired ureteric bud branching and is accompanied by downregulated expression of\n Gdnf-Ret-Wnt11<\/jats:italic>\n , a key pathway required for branching morphogenesis. Selective removal of\n Tcf21<\/jats:italic>\n from the renal stroma is also associated with attenuation of the Gdnf signaling axis and leads to a defect in ureteric bud branching, a paucity of collecting ducts, and a defect in urine concentration capacity. In contrast, deletion of\n Tcf21<\/jats:italic>\n from the cap mesenchyme leads to abnormal glomerulogenesis and massive proteinuria, but no downregulation of\n Gdnf-Ret-Wnt11<\/jats:italic>\n or obvious defect in branching.\n <\/jats:p>\n <\/jats:sec>\n \n Conclusions<\/jats:title>\n Our findings indicate that Tcf21 has distinct roles in the cap mesenchyme and stromal mesenchyme compartments during kidney development and suggest that Tcf21 regulates key molecular pathways required for branching morphogenesis.<\/jats:p>\n <\/jats:sec>","DOI":"10.1681\/asn.2017121278","type":"journal-article","created":{"date-parts":[[2018,10,30]],"date-time":"2018-10-30T10:55:28Z","timestamp":1540896928000},"page":"2795-2808","source":"Crossref","is-referenced-by-count":34,"title":["Transcription Factor 21 Is Required for Branching Morphogenesis and Regulates the Gdnf-Axis in Kidney Development"],"prefix":"10.1681","volume":"29","author":[{"given":"Shintaro","family":"Ide","sequence":"first","affiliation":[{"name":"Department of Clinical Cell Biology and Medicine, Graduate School of Medicine, Chiba University, Chiba, Japan;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gal","family":"Finer","sequence":"additional","affiliation":[{"name":"Division of Kidney Diseases, Ann and Robert H. Lurie Children\u2019s Hospital of Chicago, Chicago, Illinois;"},{"name":"Feinberg Cardiovascular and Renal Research Institute and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yoshiro","family":"Maezawa","sequence":"additional","affiliation":[{"name":"Department of Clinical Cell Biology and Medicine, Graduate School of Medicine, Chiba University, Chiba, Japan;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tuncer","family":"Onay","sequence":"additional","affiliation":[{"name":"Feinberg Cardiovascular and Renal Research Institute and"},{"name":"Division of Nephrology\/Hypertension, Northwestern University Feinberg School of Medicine, Chicago, Illinois;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tomokazu","family":"Souma","sequence":"additional","affiliation":[{"name":"Feinberg Cardiovascular and Renal Research Institute and"},{"name":"Division of Nephrology\/Hypertension, Northwestern University Feinberg School of Medicine, Chicago, Illinois;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rizaldy","family":"Scott","sequence":"additional","affiliation":[{"name":"Feinberg Cardiovascular and Renal Research Institute and"},{"name":"Division of Nephrology\/Hypertension, Northwestern University Feinberg School of Medicine, Chicago, Illinois;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kana","family":"Ide","sequence":"additional","affiliation":[{"name":"Department of Clinical Cell Biology and Medicine, Graduate School of Medicine, Chiba University, Chiba, Japan;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yoshihiro","family":"Akimoto","sequence":"additional","affiliation":[{"name":"Department of Anatomy, Kyorin University School of Medicine, Tokyo, Japan;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chengjin","family":"Li","sequence":"additional","affiliation":[{"name":"Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada; and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Minghao","family":"Ye","sequence":"additional","affiliation":[{"name":"Feinberg Cardiovascular and Renal Research Institute and"},{"name":"Division of Nephrology\/Hypertension, Northwestern University Feinberg School of Medicine, Chicago, Illinois;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xiangmin","family":"Zhao","sequence":"additional","affiliation":[{"name":"Division of Kidney Diseases, Ann and Robert H. 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