Evidence map›Paper›PMID 15258772›Full record

ArticleHistochemistry and cell biology2004

Applications of an efficient method for comparing immunogold labelling patterns in the same sets of compartments in different groups of cells.

Terry M Mayhew, Gareth Griffiths, John M Lucocq

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Article in Histochemistry and cell biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
–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

19 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
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  9. Crucial role of the small GTPase Rac1 in insulin-stimulated translocation of glucose transporter 4 to the mouse skeletal muscle sarcolemma.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2010
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  15. Aging results in increased autophagy of mitochondria and protein nitration in rat hepatocytes following heat stress.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2008
    Article
  16. Article
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  19. News and views in Histochemistry and Cell Biology.Histochemistry and cell biology · 2004
    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

3 authors.

Terry M MayhewCentre for Integrated Systems Biology and Medicine, Institute of Clinical Research and School of Biomedical Sciences, Queen's Medical Centre, E Floor, University of Nottingham, NG7 2UH, Nottingham, UK. terry.mayhew@nottingham.ac.uk
Gareth Griffiths
John M Lucocq

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quantitative immunoelectron microscopy often involves determining the distributions of gold label in different intracellular compartments and then drawing comparisons between compartments in the same sample of cells or between experimental groups of cells. In the case of within-group comparisons, recent developments in the estimation of relative labelling index and labelling density make it possible to test whether or not particular compartments are preferentially labelled. These methods are ideally suited to analysing gold label restricted to volume (organelle) or surface (membrane) compartments but may be modified to analyse label localised in mixtures of both. Here, a simple and efficient approach to drawing between-group comparisons for label associated with organelles and/or membranes is presented. The method relies on multistage random sampling of specimens (via blocks and microscopic fields) followed by simply counting gold particles associated with different compartments. The distributions of raw gold counts in different groups are then compared by contingency table analysis with statistical degrees of freedom for chi-squared values being determined by the number of compartments and the number of experimental groups of cells. Compartmental chi-squared values making substantial contributions to the total chi-squared values then identify where the main between-group differences reside. The method requires no information about compartment size (for example, organelle profile area or membrane trace length) and does not even depend critically on standardising between-group magnification. Its application is illustrated using datasets from immunolabelling studies designed to localise the KDEL receptor, phosphatidyl-inositol 4,5-bisphosphate, GLUT4 and rab4 at the electron microscopic level.

Indexed as

ImmunohistochemistryGlucose Transporter Type 4Gold ColloidGolgi ApparatusHumansMicroscopy, Electron, TransmissionMicroscopy, ImmunoelectronMonosaccharide Transport ProteinsMuscle ProteinsPhosphatidylinositol 4,5-Diphosphaterab4 GTP-Binding ProteinsReceptors, PeptideSubcellular FractionsTissue FixationGlucose Transporter Type 4Gold ColloidKDEL receptorMonosaccharide Transport ProteinsMuscle ProteinsPhosphatidylinositol 4,5-Diphosphaterab4 GTP-Binding ProteinsReceptors, PeptideSLC2A4 protein, human

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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.