Evidence map›Paper›PMID 17988971›Full record

ArticleBone2008

NHA-oc/NHA2: a mitochondrial cation-proton antiporter selectively expressed in osteoclasts.

R A Battaglino, L Pham, L R Morse, M Vokes, A Sharma, P R Odgren, M Yang, H Sasaki, P Stashenko

Abstract read
In one paragraph

Article in Bone, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

26 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Trafficking of the human NaProtein science : a publication of the Protein Society · 2026
    Article
  3. Article
  4. Article
  5. NaInternational journal of molecular sciences · 2023
    Review
  6. Allosteric links between the hydrophilic N-terminus and transmembrane core of human NaProtein science : a publication of the Protein Society · 2022
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Membrane Transport Proteins in Osteoclasts: The Ins and Outs.Frontiers in cell and developmental biology · 2021
    Review
  12. Structure of theProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Traditional and emerging roles for the SLC9 Na+/H+ exchangers.Pflugers Archiv : European journal of physiology · 2014
    Review
  18. Review
  19. Article
  20. 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

9 authors at 3 institutions in 1 country.

R A BattaglinoDepartment of Cytokine Biology, Forsyth Institute, 140 The Fenway, Boston, MA 02115, USA. rbattaglino@forsyth.org
L Pham
L R Morse
M Vokes
A Sharma
P R Odgren
M Yang
H Sasaki
P Stashenko
University of Massachusetts Chan Medical School · USForsyth County Schools · USHarvard University · US

Funding

Role of Serotonin in Osteoclast DifferentationR01DE007378 · NIDCR · FORSYTH INSTITUTE · PI STASHENKO, PHILIP · 1985 to 2005
$1.7M
NIDCR NIH HHS R01 DE007378
6 · The paper itself

Abstract

Bone resorption is regulated by a complex system of hormones and cytokines that cause osteoblasts/stromal cells and lymphocytes to produce factors including RANKL, that ultimately result in the differentiation and activation of osteoclasts, the bone resorbing cells. We used a microarray approach to identify genes upregulated in RANKL-stimulated osteoclast precursor cells. Osteoclast expression was confirmed by multiple tissue Northern and in situ hybridization analysis. Gene function studies were carried out by siRNA analysis. We identified a novel gene, which we termed nha-oc/NHA2, which is strongly upregulated during RANKL-induced osteoclast differentiation in vitro and in vivo. nha-oc/NHA2 encodes a novel cation-proton antiporter (CPA) and is the mouse orthologue of a human gene identified in a database search: HsNHA2. nha-oc/NHA2 is selectively expressed in osteoclasts. NHA-oc/NHA2 protein localizes to the mitochondria, where it mediates Na(+)-dependent changes in mitochondrial pH and Na(+) acetate induced mitochondrial passive swelling. RNA silencing of nha-oc/nha2 reduces osteoclast differentiation and resorption, suggesting a role for NHA-oc/NHA2 in these processes. nha-oc/NHA2 therefore is a novel member of the CPA family and is the first mitochondrial NHA characterized to date. nha-oc/NHA2 is also unique in that it is the first eukaryotic and tissue-specific CPA2 characterized to date. NHA-oc/NHA2 displays the expected activities of a bona fide CPA and plays a key role(s) in normal osteoclast differentiation and function.

Indexed as

Amino Acid SequenceAnimalsAntiportersCaspasesCell DifferentiationCell LineCloning, MolecularEnzyme ActivationGene Expression RegulationHumansHydrogen-Ion ConcentrationMiceMitochondriaMitochondrial SwellingMolecular Sequence DataOsteoclastsAntiportersCaspasesNHA2 protein, mouseRNA, MessengerRNA, Small InterferingSLC9B2 protein, human

Identifiers

PMID17988971
PMCPMC3593247
OpenAlexW2066150108

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.