Evidence map›Paper›PMID 24523290›Full record

ArticleMolecular biology of the cell2014

Regulation of the epithelial Ca²⁺ channel TRPV5 by reversible histidine phosphorylation mediated by NDPK-B and PHPT1.

Xinjiang Cai, Shekhar Srivastava, Sheena Surindran, Zhai Li, Edward Y Skolnik

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
–field-weighted citation impact
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

47 citing papers in PubMed.

  1. A Constellation of Fluorescent Biosensors to Illuminate the Galaxy of Protein Kinases.Chembiochem : a European journal of chemical biology · 2026
    Review
  2. Inhibition of PHPT1 by phenylarsonic acids.Dalton transactions (Cambridge, England : 2003) · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Histidine Phosphorylation: Protein Kinases and Phosphatases.International journal of molecular sciences · 2024
    Review
  8. [Progress in enrichment methods for proteinSe pu = Chinese journal of chromatography · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. The role of TRPV channels in osteoporosis.Molecular biology reports · 2022
    Review
  17. Review
  18. Article
  19. Article
  20. NME/NM23/NDPK and Histidine Phosphorylation.International journal of molecular sciences · 2020
    Review
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

5 authors.

Xinjiang CaiDivision of Nephrology, New York University Langone Medical Center, New York, NY 10016 Department of Molecular Pathogenesis, New York University Langone Medical Center, New York, NY 10016 The Helen L. and Martin S. Kimmel Center for Biology and Medicine at the Skirball Institute for Biomolecular Medicine, New York University Langone Medical Center, New York, NY 10016 Department of Biochemistry and Molecular Pharmacology, New York University Langone Medical Center, New York, NY 10016.
Shekhar Srivastava
Sheena Surindran
Zhai Li
Edward Y Skolnik

Funding

TRIM27 is a new negative regulator of CD4 T cells and Mast cells.R01GM099873 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SKOLNIK, EDWARD Y · 2012 to 2015
$1.5M
NIGMS NIH HHS R01 GM099873
6 · The paper itself

Abstract

The kidney, together with bone and intestine, plays a crucial role in maintaining whole-body calcium (Ca(2+)) homoeostasis, which is primarily mediated by altering the reabsorption of Ca(2+) filtered by the glomerulus. The transient receptor potential-vanilloid-5 (TRPV5) channel protein forms a six- transmembrane Ca(2+)-permeable channel that regulates urinary Ca(2+) excretion by mediating active Ca(2+) reabsorption in the distal convoluted tubule of the kidney. Here we show that the histidine kinase, nucleoside diphosphate kinase B (NDPK-B), activates TRPV5 channel activity and Ca(2+) flux, and this activation requires histidine 711 in the carboxy-terminal tail of TRPV5. In addition, the histidine phosphatase, protein histidine phosphatase 1, inhibits NDPK-B-activated TRPV5 in inside/out patch experiments. This is physiologically relevant to Ca(2+) reabsorption in vivo, as short hairpin RNA knockdown of NDPK-B leads to decreased TRPV5 channel activity, and urinary Ca(2+) excretion is increased in NDPK-B(-/-) mice fed a high-Ca(2+) diet. Thus these findings identify a novel mechanism by which TRPV5 and Ca(2+) reabsorption is regulated by the kidney and support the idea that histidine phosphorylation plays other, yet-uncovered roles in mammalian biology.

Indexed as

Amino Acid SequenceAnimalsCalciumCalcium ChannelsCalcium SignalingCell LineDogsHEK293 CellsHistidineHomeostasisHumansKidney GlomerulusMadin Darby Canine Kidney CellsMiceMice, Inbred C57BLMice, KnockoutCalciumCalcium ChannelsHistidineNDPK-B protein, humanNucleoside-Diphosphate KinasePhosphoric Monoester HydrolasesPHPT1 protein, humanRNA, Small InterferingTRPV5 protein, humanTRPV Cation Channels

Identifiers

PMID24523290
PMCPMC3982990

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Registered trials

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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.