Literature DB >> 17658596

Taking tissue samples from the placenta: an illustration of principles and strategies.

T M Mayhew1.   

Abstract

Tissue samples are removed from placentas for a variety of reasons associated with a host of investigative techniques, including chorionic villus sampling, villus explant culture, cell culture, proteomic analysis, gene expression profiling, microscopy and morphometry. Apart from the latter, especially stereological analysis, many studies provide extremely limited information on how the samples were selected. At worst, we learn little more than the placenta was sampled. Sometimes, studies provide sufficient detail to reveal flaws in sampling, e.g. the selection of placentomes based on size rather than mere presence. Occasionally, the reader is informed, without further explanation, that representative samples were taken or that samples from placentas in different study groups were taken from standard or similar sites. Such statements raise doubts about the unbiasedness of the sampling process, leave the reader in ignorance of the quality of the final sample, thwart attempts at achieving study repeatability and compromise interpretations of the validity of study outcomes. And yet study outcomes depend critically on the selection process because sampling influences study errors, notably precision (random error) and bias (systematic error). This article aims to review the basic principles and virtues of random sampling in general and the practical utilities of variants of it. For many functional and structural studies, it suffices to randomise the positions of tissue samples but, in certain structural studies, orientation must also be randomised. Therefore, sampling tools for stereological estimation of membrane surface areas, tubule lengths and layer thicknesses are mentioned. Although emphasis is accorded to the placenta, the principles apply equally well to other organs and to lower levels of organisation including the subcellular. It is hoped that this review will inform future study designs, encourage greater transparency and facilitate sampling improvements.

Mesh:

Year:  2007        PMID: 17658596     DOI: 10.1016/j.placenta.2007.05.010

Source DB:  PubMed          Journal:  Placenta        ISSN: 0143-4004            Impact factor:   3.481


  54 in total

1.  Survival in critical illness is associated with early activation of mitochondrial biogenesis.

Authors:  Jane E Carré; Jean-Christophe Orban; Lorenza Re; Karen Felsmann; Wiebke Iffert; Michael Bauer; Hagir B Suliman; Claude A Piantadosi; Terry M Mayhew; Patrick Breen; Martin Stotz; Mervyn Singer
Journal:  Am J Respir Crit Care Med       Date:  2010-06-10       Impact factor: 21.405

2.  Quantitative PCR pitfalls: the case of the human placenta.

Authors:  Dave Lanoix; Andrée-Anne Lacasse; Joey St-Pierre; Sean C Taylor; Maude Ethier-Chiasson; Julie Lafond; Cathy Vaillancourt
Journal:  Mol Biotechnol       Date:  2012-11       Impact factor: 2.695

Review 3.  Mapping the distributions and quantifying the labelling intensities of cell compartments by immunoelectron microscopy: progress towards a coherent set of methods.

Authors:  Terry M Mayhew
Journal:  J Anat       Date:  2011-10-17       Impact factor: 2.610

4.  Quantifying immunogold labelling patterns of cellular compartments when they comprise mixtures of membranes (surface-occupying) and organelles (volume-occupying).

Authors:  Terry M Mayhew; John M Lucocq
Journal:  Histochem Cell Biol       Date:  2008-01-05       Impact factor: 4.304

5.  Allometry of left ventricular myocardial innervation.

Authors:  Julia Schipke; Terry M Mayhew; Christian Mühlfeld
Journal:  J Anat       Date:  2013-12-10       Impact factor: 2.610

6.  Impaired mitochondrial function in human placenta with increased maternal adiposity.

Authors:  James Mele; Sribalasubashini Muralimanoharan; Alina Maloyan; Leslie Myatt
Journal:  Am J Physiol Endocrinol Metab       Date:  2014-07-15       Impact factor: 4.310

7.  Multiple-labelling immunoEM using different sizes of colloidal gold: alternative approaches to test for differential distribution and colocalization in subcellular structures.

Authors:  Terry M Mayhew; John M Lucocq
Journal:  Histochem Cell Biol       Date:  2011-02-16       Impact factor: 4.304

8.  An official research policy statement of the American Thoracic Society/European Respiratory Society: standards for quantitative assessment of lung structure.

Authors:  Connie C W Hsia; Dallas M Hyde; Matthias Ochs; Ewald R Weibel
Journal:  Am J Respir Crit Care Med       Date:  2010-02-15       Impact factor: 21.405

9.  Using dynamic contrast-enhanced MRI to quantitatively characterize maternal vascular organization in the primate placenta.

Authors:  Antonio E Frias; Matthias C Schabel; Victoria H J Roberts; Alina Tudorica; Peta L Grigsby; Karen Y Oh; Christopher D Kroenke
Journal:  Magn Reson Med       Date:  2014-04-18       Impact factor: 4.668

Review 10.  A stereological perspective on placental morphology in normal and complicated pregnancies.

Authors:  Terry M Mayhew
Journal:  J Anat       Date:  2008-01-02       Impact factor: 2.610

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