Evidence map›Paper›PMID 19151209›Full record

ReviewThe Journal of experimental biology2009

NHE(VNAT): an H+ V-ATPase electrically coupled to a Na+:nutrient amino acid transporter (NAT) forms an Na+/H+ exchanger (NHE).

William R Harvey, Dmitri Y Boudko, Mark R Rheault, Bernard A Okech

Open access · greenAbstract readReview
In one paragraph

Review in The Journal of experimental biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Mechanisms of NaFrontiers in physiology · 2022
    Review
  3. Article
  4. Article
  5. NaThe Journal of physiology · 2017
    Article
  6. Article
  7. Review
  8. The physiological response of larval Chironomus riparius (Meigen) to abrupt brackish water exposure.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2011
    Article
  9. Article
  10. Review
  11. Article
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

4 authors at 1 institution in 1 country.

William R HarveyWhitney Laboratory for Marine Bioscience, University of Florida, St Augustine, FL 32080, USA. wharvey@whitney.ufl.edu
Dmitri Y Boudko
Mark R Rheault
Bernard A Okech
University of Florida · US

Funding

PHYSIOLOGY OF INSECT AMINO ACID TRANSPORTR01AI030464 · NIAID · UNIVERSITY OF FLORIDA · PI BOUDKO, DMITRI Y. · 1991 to 2008
$2.1M
Transport Physiology of Disease Vector MosquitoesR01AI052436 · NIAID · UNIVERSITY OF FLORIDA · PI HARVEY, WILLIAM R · 2003 to 2007
$1.4M
Physiology of Insect Amino Acid TransportR56AI030464 · NIAID · ROSALIND FRANKLIN UNIV OF MEDICINE & SCI · PI BOUDKO, DMITRI Y. · 2010 to 2010
$322k
NIAID NIH HHS AI-30464NIAID NIH HHS AI-52436NIAID NIH HHS R56 AI030464
6 · The paper itself

Abstract

Glycolysis, the citric acid cycle and other metabolic pathways of living organisms generate potentially toxic acids within all cells. One ubiquitous mechanism for ridding cells of the acids is to expel H(+) in exchange for extracellular Na(+), mediated by electroneutral transporters called Na(+)/H(+) exchangers (NHEs) that are driven by Na(+) concentration gradients. The exchange must be important because the human genome contains 10 NHEs along with two Na(+)/H(+) antiporters (NHAs). By contrast, the genomes of two principal disease vector mosquitoes, Anopheles gambiae and Aedes aegypti, contain only three NHEs along with the two NHAs. This shortfall may be explained by the presence of seven nutrient amino acid transporters (NATs) in the mosquito genomes. NATs transport Na(+) stoichiometrically linked to an amino acid into the cells by a process called symport or co-transport. Three of the mosquito NATs and two caterpillar NATs have previously been investigated after heterologous expression in Xenopus laevis oocytes and were found to be voltage driven (electrophoretic). Moreover, the NATs are present in the same membrane as the H(+) V-ATPase, which generates membrane potentials as high as 120 mV. We review evidence that the H(+) V-ATPase moves H(+) out of the cells and the resulting membrane potential (V(m)) drives Na(+) linked to an amino acid into the cells via a NAT. The H(+) efflux by the V-ATPase and Na(+) influx by the NAT comprise the same ion exchange as that mediated by an NHE; so the V and NAT working together constitute an NHE that we call NHE(VNAT). As the H(+) V-ATPase is widely distributed in mosquito epithelial cells and there are seven NATs in the mosquito genomes, there are potentially seven NHE(VNAT)s that could replace the missing NHEs. We review published evidence in support of this hypothesis and speculate about broader functions of NHE(VNAT)s.

Indexed as

Models, MolecularPhylogenyAmino Acid SequenceAmino Acid Transport SystemsAmino Acid Transport Systems, NeutralAnimalsCulicidaeInsect ProteinsIon TransportMembrane PotentialsMolecular Sequence DataSodiumSodium-Hydrogen ExchangersVacuolar Proton-Translocating ATPasesAmino Acid Transport SystemsAmino Acid Transport Systems, NeutralInsect ProteinsKAAT1 protein, insectSodiumSodium-Hydrogen ExchangersVacuolar Proton-Translocating ATPases

Identifiers

PMID19151209
PMCPMC2727077
OpenAlexW1999036631

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.