Literature DB >> 29315540

Stereological analysis of individual lung lobes during normal and aberrant mouse lung alveolarisation.

Tuong-Van Hoang1,2, Claudio Nardiello1,2, David E Surate Solaligue1,2, José Alberto Rodríguez-Castillo1,2, Philipp Rath1, Konstantin Mayer2, István Vadász2, Susanne Herold2, Kathrin Ahlbrecht1,2, Werner Seeger1,2, Rory E Morty1,2.   

Abstract

The quantitative assessment of the lung architecture forms the foundation of many studies on lung development and lung diseases, where parameters such as alveoli number, alveolar size, and septal thickness are quantitatively influenced by developmental or pathological processes. Given the pressing need for robust data that describe the lung structure, there is currently much enthusiasm for the development and refinement of methodological approaches for the unbiased assessment of lung structure with improved precision. The advent of stereological methods highlights one such approach. However, design-based stereology is both expensive and time-demanding. The objective of this study was to examine whether 'limited' stereological analysis, such as the stereological analysis of a single mouse lung lobe, may serve as a surrogate for studies on whole, intact mouse lungs; both in healthy lungs and in diseased lungs, using an experimental animal model of bronchopulmonary dysplasia (BPD). This served the dual-function of exploring BPD pathobiology, asking whether there are regional (lobar) differences in the responses of developing mouse lungs to oxygen injury, by examining each mouse lung lobe separately in the BPD model. Hyperoxia exposure resulted in decreased alveolar density, alveoli number, and gas-exchange surface area in all five mouse lung lobes, and increased the arithmetic mean septal thickness in all mouse lung lobes except the lobus cardialis. The data presented here suggest that - in healthy developing mice - a single mouse lung lobe might serve as a surrogate for studies on whole, intact mouse lungs. This is not the case for oxygen-injured developing mouse lungs, where a single lobe would not be suitable as a surrogate for the whole, intact lung. Furthermore, as the total number of alveoli can only be determined by an analysis of the entire lung, and given regional differences in lung structure, particularly under pathological conditions, the stereological assessment of the whole, intact lung remains desirable.
© 2018 Anatomical Society.

Entities:  

Keywords:  alveolarisation; bronchopulmonary dysplasia; lobe; lung; stereology

Mesh:

Year:  2018        PMID: 29315540      PMCID: PMC5807959          DOI: 10.1111/joa.12773

Source DB:  PubMed          Journal:  J Anat        ISSN: 0021-8782            Impact factor:   2.610


  32 in total

1.  Caffeine administration modulates TGF-β signaling but does not attenuate blunted alveolarization in a hyperoxia-based mouse model of bronchopulmonary dysplasia.

Authors:  Philipp Rath; Claudio Nardiello; David E Surate Solaligue; Ronald Agius; Ivana Mižíková; Sebastian Hühn; Konstantin Mayer; István Vadász; Susanne Herold; Frank Runkel; Werner Seeger; Rory E Morty
Journal:  Pediatr Res       Date:  2017-01-31       Impact factor: 3.756

Review 2.  Quantitative microscopy of the lung: a problem-based approach. Part 2: stereological parameters and study designs in various diseases of the respiratory tract.

Authors:  Christian Mühlfeld; Matthias Ochs
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2013-05-24       Impact factor: 5.464

Review 3.  A review of recent developments and applications of morphometry/stereology in lung research.

Authors:  Christian Mühlfeld; Jan Hegermann; Christoph Wrede; Matthias Ochs
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2015-07-17       Impact factor: 5.464

4.  Stereological monitoring of mouse lung alveolarization from the early postnatal period to adulthood.

Authors:  Agnieszka Pozarska; José Alberto Rodríguez-Castillo; David E Surate Solaligue; Aglaia Ntokou; Philipp Rath; Ivana Mižíková; Alicia Madurga; Konstantin Mayer; István Vadász; Susanne Herold; Katrin Ahlbrecht; Werner Seeger; Rory E Morty
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2017-03-17       Impact factor: 5.464

Review 5.  Quantitative microscopy of the lung: a problem-based approach. Part 1: basic principles of lung stereology.

Authors:  Matthias Ochs; Christian Mühlfeld
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2013-04-26       Impact factor: 5.464

6.  Application of the Cavalieri principle and vertical sections method to lung: estimation of volume and pleural surface area.

Authors:  R P Michel; L M Cruz-Orive
Journal:  J Microsc       Date:  1988-05       Impact factor: 1.758

7.  A simple method for volumetry of organs in quantitative stereology.

Authors:  W Scherle
Journal:  Mikroskopie       Date:  1970-06

8.  Optimizing sampling efficiency of stereological studies in biology: or 'do more less well!'.

Authors:  H J Gundersen; R Osterby
Journal:  J Microsc       Date:  1981-01       Impact factor: 1.758

Review 9.  Looking ahead: where to next for animal models of bronchopulmonary dysplasia?

Authors:  Claudio Nardiello; Ivana Mižíková; Rory E Morty
Journal:  Cell Tissue Res       Date:  2016-12-05       Impact factor: 5.249

Review 10.  Development of the lung.

Authors:  Johannes C Schittny
Journal:  Cell Tissue Res       Date:  2017-01-31       Impact factor: 5.249

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