Evidence map›Paper›PMID 27043644›Full record

ArticleBiosensors2016

Measurement of Rapid Amiloride-Dependent pH Changes at the Cell Surface Using a Proton-Sensitive Field-Effect Transistor.

Daniel Schaffhauser, Michael Fine, Miyuki Tabata, Tatsuro Goda, Yuji Miyahara

Open access · goldAbstract read
In one paragraph

Article in Biosensors, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
3.8field-weighted citation impact, top 9% 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

4 citing papers in PubMed, 21 citations in OpenAlex.

  1. Control of interface functions in solid-state biosensors for stable detection of molecular recognition.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2024
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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 at 2 institutions in 2 countries.

Daniel SchaffhauserInstitute of Biomaterials & Bioengineering, Tokyo Medical and Dental University, Bldg 21-4-403B, 2-3-10 Kanda-Surugadai, Chiyoda, Tokyo 101-0062, Japan. danielschaffhauser@gmail.com.
Michael FineDepartment of Physiology, UT Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390, USA. michael.fine@utsouthwestern.edu.
Miyuki TabataInstitute of Biomaterials & Bioengineering, Tokyo Medical and Dental University, Bldg 21-4-403B, 2-3-10 Kanda-Surugadai, Chiyoda, Tokyo 101-0062, Japan. tabata.bsr@tmd.ac.jp.
Tatsuro GodaInstitute of Biomaterials & Bioengineering, Tokyo Medical and Dental University, Bldg 21-4-403B, 2-3-10 Kanda-Surugadai, Chiyoda, Tokyo 101-0062, Japan. goda.bsr@tmd.ac.jp.
Yuji MiyaharaInstitute of Biomaterials & Bioengineering, Tokyo Medical and Dental University, Bldg 21-4-403B, 2-3-10 Kanda-Surugadai, Chiyoda, Tokyo 101-0062, Japan. miyahara.bsr@tmd.ac.jp.
Tokyo Medical and Dental University · JPThe University of Texas Southwestern Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present a novel method for the rapid measurement of pH fluxes at close proximity to the surface of the plasma membrane in mammalian cells using an ion-sensitive field-effect transistor (ISFET). In conjuction with an efficient continuous superfusion system, the ISFET sensor was capable of recording rapid changes in pH at the cells' surface induced by intervals of ammonia loading and unloading, even when using highly buffered solutions. Furthermore, the system was able to isolate physiologically relevant signals by not only detecting the transients caused by ammonia loading and unloading, but display steady-state signals as would be expected by a proton transport-mediated influence on the extracellular proton-gradient. Proof of concept was demonstrated through the use of 5-(N-ethyl-N-isopropyl)amiloride (EIPA), a small molecule inhibitor of sodium/hydrogen exchangers (NHE). As the primary transporter responsible for proton balance during cellular regulation of pH, non-electrogenic NHE transport is notoriously difficult to detect with traditional methods. Using the NHE positive cell lines, Chinese hamster ovary (CHO) cells and NHE3-reconstituted mouse skin fibroblasts (MSF), the sensor exhibited a significant response to EIPA inhibition, whereas NHE-deficient MSF cells were unaffected by application of the inhibitor.

Indexed as

Biosensing TechniquesHydrogen-Ion ConcentrationIon TransportProtonsAmilorideAmmoniaAnimalsCell MembraneCHO CellsCricetulusMiceAmilorideAmmoniaProtonsamilorideammoniaCHOEIPAISFETMSFNHEpHproton

Identifiers

PMID27043644
PMCPMC4931471
OpenAlexW2324440809

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.