Literature DB >> 28927826

Developmental plasticity and stability in the tracheal networks supplying Drosophila flight muscle in response to rearing oxygen level.

Jon F Harrison1, James S Waters2, Taylor A Biddulph3, Aleksandra Kovacevic4, C Jaco Klok5, John J Socha6.   

Abstract

While it is clear that the insect tracheal system can respond in a compensatory manner to both hypoxia and hyperoxia, there is substantial variation in how different parts of the system respond. However, the response of tracheal structures, from the tracheoles to the largest tracheal trunks, have not been studied within one species. In this study, we examined the effect of larval/pupal rearing in hypoxia, normoxia, and hyperoxia (10, 21 or 40kPa oxygen) on body size and the tracheal supply to the flight muscles of Drosophila melanogaster, using synchrotron radiation micro-computed tomography (SR-µCT) to assess flight muscle volumes and the major tracheal trunks, and confocal microscopy to assess the tracheoles. Hypoxic rearing decreased thorax length whereas hyperoxic-rearing decreased flight muscle volumes, suggestive of negative effects of both extremes. Tomography at the broad organismal scale revealed no evidence for enlargement of the major tracheae in response to lower rearing oxygen levels, although tracheal size scaled with muscle volume. However, using confocal imaging, we found a strong inverse relationship between tracheole density within the flight muscles and rearing oxygen level, and shorter tracheolar branch lengths in hypoxic-reared animals. Although prior studies of larger tracheae in other insects indicate that axial diffusing capacity should be constant with sequential generations of branching, this pattern was not found in the fine tracheolar networks, perhaps due to the increasing importance of radial diffusion in this regime. Overall, D. melanogaster responded to rearing oxygen level with compensatory morphological changes in the small tracheae and tracheoles, but retained stability in most of the other structural components of the tracheal supply to the flight muscles.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Developmental plasticity; Flight muscle; Gas exchange; Oxygen; Tracheae; Tracheoles

Mesh:

Substances:

Year:  2017        PMID: 28927826     DOI: 10.1016/j.jinsphys.2017.09.006

Source DB:  PubMed          Journal:  J Insect Physiol        ISSN: 0022-1910            Impact factor:   2.354


  4 in total

1.  Micro-computed tomography as a platform for exploring Drosophila development.

Authors:  Todd A Schoborg; Samantha L Smith; Lauren N Smith; H Douglas Morris; Nasser M Rusan
Journal:  Development       Date:  2019-12-11       Impact factor: 6.868

2.  Analysis of Drosophila cardiac hypertrophy by microcomputerized tomography for genetic dissection of heart growth mechanisms.

Authors:  Courtney E Petersen; Benjamin A Tripoli; Todd A Schoborg; Jeremy T Smyth
Journal:  Am J Physiol Heart Circ Physiol       Date:  2021-12-24       Impact factor: 4.733

3.  Tracheal branching in ants is area-decreasing, violating a central assumption of network transport models.

Authors:  Ian J Aitkenhead; Grant A Duffy; Citsabehsan Devendran; Michael R Kearney; Adrian Neild; Steven L Chown
Journal:  PLoS Comput Biol       Date:  2020-04-30       Impact factor: 4.475

4.  Cuticular modified air sacs underlie white coloration in the olive fruit fly, Bactrocera oleae.

Authors:  Manuela Rebora; Gianandrea Salerno; Silvana Piersanti; Alexander Kovalev; Stanislav Gorb
Journal:  Commun Biol       Date:  2021-07-16
  4 in total

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