Evidence map›Paper›PMID 26984496›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Soluble (pro)renin receptor via β-catenin enhances urine concentration capability as a target of liver X receptor.

Xiaohan Lu, Fei Wang, Chuanming Xu, Sunny Soodvilai, Kexin Peng, Jiahui Su, Long Zhao, Kevin T Yang, Yumei Feng, Shu-Feng Zhou and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
11.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

67 citing papers in PubMed, 100 citations in OpenAlex.

  1. Novel Roles of GPCRs in the Renal Collecting Duct.Physiology (Bethesda, Md.) · 2026
    Review
  2. Transcriptional regulatory factors of the Aqp2 gene.Kidney research and clinical practice · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. The soluble (pro)renin receptor promotes a preeclampsia-like phenotype both in vitro and in vivo.Hypertension research : official journal of the Japanese Society of Hypertension · 2024
    Article
  7. Article
  8. Article
  9. Review
  10. Mapping the protein binding site of the (pro)renin receptor using in silico 3D structural analysis.Hypertension research : official journal of the Japanese Society of Hypertension · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Role of (pro)renin receptor in cyclosporin A-induced nephropathy.American journal of physiology. Renal physiology · 2022
    Article
  18. Article
  19. Article
  20. Soluble (Pro)Renin Receptor as a Negative Regulator of NCC (NaHypertension (Dallas, Tex. : 1979) · 2021
    Article

7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 2 countries.

Xiaohan LuDepartment of Internal Medicine, University of Utah, Salt Lake City, UT 84112; Veterans Affairs Medical Center, Salt Lake City, UT 84108; Institute of Hypertension, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, People's Republic of China;
Fei WangInstitute of Hypertension, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, People's Republic of China; Department of Internal Medicine, University of Utah, Salt Lake City, UT 84112; Veterans Affairs Medical Center, Salt Lake City, UT 84108;
Chuanming XuInstitute of Hypertension, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, People's Republic of China;
Sunny SoodvilaiDepartment of Internal Medicine, University of Utah, Salt Lake City, UT 84112; Veterans Affairs Medical Center, Salt Lake City, UT 84108;
Kexin PengDepartment of Internal Medicine, University of Utah, Salt Lake City, UT 84112; Veterans Affairs Medical Center, Salt Lake City, UT 84108; Institute of Hypertension, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, People's Republic of China;
Jiahui SuInstitute of Hypertension, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, People's Republic of China;
Long ZhaoDepartment of Internal Medicine, University of Utah, Salt Lake City, UT 84112; Veterans Affairs Medical Center, Salt Lake City, UT 84108;
Kevin T YangDepartment of Internal Medicine, University of Utah, Salt Lake City, UT 84112; Veterans Affairs Medical Center, Salt Lake City, UT 84108;
Yumei FengDepartment of Pharmacology, University of Nevada School of Medicine, Reno, NV 89557; Department of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV 89557;
Shu-Feng ZhouDepartment of Pharmaceutical Sciences, College of Pharmacy, University of South Florida, Tampa, FL 33620;
Jan-Åke GustafssonDepartment of Biology and Biochemistry, University of Houston, Houston, TX 77004 jgustafsson@uh.edu Tianxin.Yang@hsc.utah.edu.
Tianxin YangDepartment of Internal Medicine, University of Utah, Salt Lake City, UT 84112; Veterans Affairs Medical Center, Salt Lake City, UT 84108; Institute of Hypertension, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, People's Republic of China; jgustafsson@uh.edu Tianxin.Yang@hsc.utah.edu.
Sun Yat-sen University · CNVeterans Health Administration · USUniversity of Utah · USUniversity of Houston · USUniversity of Nevada, Reno · USUniversity of South Florida · US

Funding

The Neural Mechanisms of HypertensionR01HL122770 · NHLBI · UNIVERSITY OF ROCHESTER · PI EARLEY, SCOTT, FENG EARLEY, YUMEI · 2015 to 2023
$4.2M
Interaction of PGE2 and intrarenal RAS in AngII-induced hypertensionR01DK104072 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI YANG, TIANXIN · 2015 to 2025
$3.7M
Control of collecting duct function by lipid-derived factors in obesityR01DK094956 · NIDDK · UNIVERSITY OF UTAH · PI YANG, TIANXIN · 2013 to 2017
$1.6M
NHLBI NIH HHS R01 HL122770NIDDK NIH HHS DK094956NIDDK NIH HHS DK104072NIDDK NIH HHS R01 DK094956NIDDK NIH HHS R01 DK104072PHS HHS NHLBI/R01HL122770
6 · The paper itself

Abstract

The extracellular domain of the (pro)renin receptor (PRR) is cleaved to produce a soluble (pro)renin receptor (sPRR) that is detected in biological fluid and elevated under certain pathological conditions. The present study was performed to define the antidiuretic action of sPRR and its potential interaction with liver X receptors (LXRs), which are known regulators of urine-concentrating capability. Water deprivation consistently elevated urinary sPRR excretion in mice and humans. A template-based algorithm for protein-protein interaction predicted the interaction between sPRR and frizzled-8 (FZD8), which subsequently was confirmed by coimmunoprecipitation. A recombinant histidine-tagged sPRR (sPRR-His) in the nanomolar range induced a remarkable increase in the abundance of renal aquaporin 2 (AQP2) protein in primary rat inner medullary collecting duct cells. The AQP2 up-regulation relied on sequential activation of FZD8-dependent β-catenin signaling and cAMP-PKA pathways. Inhibition of FZD8 or tankyrase in rats induced polyuria, polydipsia, and hyperosmotic urine. Administration of sPRR-His alleviated the symptoms of diabetes insipidus induced in mice by vasopressin 2 receptor antagonism. Administration of the LXR agonist TO901317 to C57/BL6 mice induced polyuria and suppressed renal AQP2 expression associated with reduced renal PRR expression and urinary sPRR excretion. Administration of sPRR-His reversed most of the effects of TO901317. In cultured collecting duct cells, TO901317 suppressed PRR protein expression, sPRR release, and PRR transcriptional activity. Overall we demonstrate, for the first time to our knowledge, that sPRR exerts antidiuretic action via FZD8-dependent stimulation of AQP2 expression and that inhibition of this pathway contributes to the pathogenesis of diabetes insipidus induced by LXR agonism.

Indexed as

AnimalsAquaporin 2Benzenesulfonamidesbeta CateninDiabetes InsipidusFluorocarbonsHydrocarbons, FluorinatedLiver X ReceptorsMaleMice, Inbred C57BLOrphan Nuclear ReceptorsOsmosisProrenin ReceptorRats, Sprague-DawleyReceptors, Cell SurfaceRecombinant ProteinsAqp2 protein, ratAquaporin 2Benzenesulfonamidesbeta CateninCTNNB1 protein, mouseCtnnb1 protein, ratFluorocarbonsFZD8 protein, ratHydrocarbons, FluorinatedLiver X ReceptorsOrphan Nuclear ReceptorsProrenin ReceptorReceptors, Cell SurfaceRecombinant ProteinsSulfonamidesT0901317aquaporin-2frizzled-8liver X receptorsoluble (pro)renin receptorβ-catenin

Identifiers

PMID26984496
PMCPMC4822598
OpenAlexW2297371006

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.