Evidence map›Paper›PMID 24798000›Full record

ArticleJournal of visualized experiments : JoVE2014

Simultaneous pH measurement in endocytic and cytosolic compartments in living cells using confocal microscopy.

Fabrice Lucien, Kelly Harper, Pierre-Paul Pelletier, Leonid Volkov, Claire M Dubois

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. The journal of physical chemistry. B · 2025
    Article
  2. Article
  3. Review
  4. International journal of molecular sciences · 2020
    Article
  5. Article
  6. Article
  7. Targeting endosomal pH for cancer chemotherapy.Molecular & cellular oncology · 2018
    Article
  8. Article
  9. Article
  10. 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

5 authors at 1 institution in 1 country.

Fabrice LucienDepartment of Pediatrics, Faculty of Medicine and Health Sciences, Université de Sherbrooke.
Kelly HarperDepartment of Pediatrics, Faculty of Medicine and Health Sciences, Université de Sherbrooke.
Pierre-Paul PelletierDepartment of Pediatrics, Faculty of Medicine and Health Sciences, Université de Sherbrooke.
Leonid VolkovBiophotonics Core Facility, Centre de Recherche Clinique Etienne-Le Bel.
Claire M DuboisDepartment of Pediatrics, Faculty of Medicine and Health Sciences, Université de Sherbrooke; Claire.Dubois@usherbrooke.ca.
Université de Sherbrooke · CA

Funding

Canadian Institutes of Health Research MOP-126173
6 · The paper itself

Abstract

Intracellular pH is tightly regulated and differences in pH between the cytoplasm and organelles have been reported(1). Regulation of cellular pH is crucial for homeostatic control of physiological processes that include: protein, DNA and RNA synthesis, vesicular trafficking, cell growth and cell division. Alterations in cellular pH homeostasis can lead to detrimental functional changes and promote progression of various diseases(2). Various methods are available for measuring intracellular pH but very few of these allow simultaneous measurement of pH in the cytoplasm and in organelles. Here, we describe in detail a rapid and accurate method for the simultaneous measurement of cytoplasmic and organellar pH by using confocal microscopy on living cells(3). This goal is achieved with the use of two pH-sensing ratiometric dyes that possess selective cellular compartment partitioning. For instance, SNARF-1 is compartmentalized inside the cytoplasm whereas HPTS is compartmentalized inside endosomal/lysosomal organelles. Although HPTS is commonly used as a cytoplasmic pH indicator, this dye can specifically label vesicles along the endosomal-lysosomal pathway after being taken up by pinocytosis(3,4). Using these pH-sensing probes, it is possible to simultaneously measure pH within the endocytic and cytoplasmic compartments. The optimal excitation wavelength of HPTS varies depending on the pH while for SNARF-1, it is the optimal emission wavelength that varies. Following loading with SNARF-1 and HPTS, cells are cultured in different pH-calibrated solutions to construct a pH standard curve for each probe. Cell imaging by confocal microscopy allows elimination of artifacts and background noise. Because of the spectral properties of HPTS, this probe is better suited for measurement of the mildly acidic endosomal compartment or to demonstrate alkalinization of the endosomal/lysosomal organelles. This method simplifies data analysis, improves accuracy of pH measurements and can be used to address fundamental questions related to pH modulation during cell responses to external challenges.

Indexed as

Cell Line, TumorCytosolFibrosarcomaHumansHydrogen-Ion ConcentrationMicroscopy, ConfocalOrganelles

Identifiers

PMID24798000
PMCPMC4183071
OpenAlexW1977436561

What OpenQuestion holds

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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.