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Inicio Porto Biomedical Journal Lung branching morphogenesis, in the chicken model, is accompanied by temporal m...
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Vol. 2. Issue 5.
Pages 222-223 (September - October 2017)
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Vol. 2. Issue 5.
Pages 222-223 (September - October 2017)
PS185
Open Access
Lung branching morphogenesis, in the chicken model, is accompanied by temporal metabolic changes
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H. Fernandes-Silva1,2,
Corresponding author
hugomiguelfsilva@gmail.com

Corresponding author.
, M.G. Alves3,4, J. Correia-Pinto1,2,5, P.F. Oliveira3,4,6,7, R.S. Moura1,2
1 Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal
2 ICVS/3B's – PT Government Associate Laboratory, 4710-057 Braga/Guimarães, Portugal
3 Unit for Multidisciplinary Research in Biomedicine (UMIB), Institute of Biomedical Sciences Abel Salazar (ICBAS), University of Porto, 4050-313 Porto, Portugal
4 Department of Microscopy, Institute of Biomedical Sciences Abel Salazar (ICBAS), University of Porto, 4050-313 Porto, Portugal
5 Department of Pediatric Surgery, Hospital de Braga, 4710-243 Braga, Portugal
6 i3S - Instituto de Inovação e Investigação em Saúde, University of Porto, 4050-313 Porto, Portugal
7 Department of Genetics, Faculty of Medicine (FMUP), University of Porto
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Aim: In this work, we characterized, for the first time, the metabolic profile of chick lung branching in early stages of development: b1, b2 and b3 (1, 2 or 3 secondary bronchi, respectively).

Introduction: Pulmonary development is a complex process that depends on the activation of conserved signaling pathways that regulate cellular processes such as proliferation, differentiation and migration.1–3 These cellular processes require high amounts of energy and nutrients to form new biomass.4,5 However, the metabolic changes that occur during lung branching morphogenesis have not been described so far.

Methods: Ex vivo lung explant culture was performed and the medium collected to analyze the production/consumption of metabolic intermediates associated with glucose catabolism (lactate, acetate, alanine), by 1H-NMR. qPCR was performed to assess the expression levels of key enzymes and transporters from the correspondent metabolic pathways.

Results: The results showed that the major variations occur from stage b1 to stage b3. In b3 there is an increase in lactate and acetate production. Still, glucose consumption is maintained from b1 to b3 stage, with a concurrent decrease of glucose transporter 3 (glut3) transcript levels. Hexokinase 1 (hk1) levels also decrease in b3 stage (as compared to b2). This phenomenon suggests an increase in the glycolytic efficiency and a shift to lactic acid production (in detriment of mitochondrial respiration). In fact, we observed a decrease on pyruvate dehydrogenase B (pdhB) and an increase in lactate dehydrogenase A (ldhA) expression levels in b3 stage (as compared to b2), while lactate dehydrogenase B (ldhB) levels decrease.

Conclusion: This study describes, for the first time, the temporal metabolic changes associated with chick pulmonary branching. It seems that glycolytic efficiency is increased and Krebs cycle metabolism shifts to lactate production along development. Furthermore, acetate and lactate are potentially seen as metabolic biomarkers of lung development.

Acknowledgements: This work has been funded by FEDER funds, through the Competitiveness Factors Operational Programme (COMPETE), and by National funds, through the Foundation for Science and Technology (FCT), under the scope of the project POCI-01-0145-FEDER-007038; and by the project NORTE-01-0145-FEDER-000013, supported by the Northern Portugal Regional Operational Programme (NORTE 2020), under the Portugal 2020 Partnership Agreement, through the European Regional Development Fund (FEDER). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References
[1]
D.M. Ornitz, et al.
Cold Spring Harb Perspect Biol, 4 (2012),
pii:a008318
[2]
R.S. Moura, et al.
[3]
R.S. Moura, et al.
Histochem Cell Biol, 146 (2016), pp. 457-466
[4]
T. Ito, et al.
Histol Histopathol, 14 (1999), pp. 895-904
[5]
P.F. Oliveira, et al.
Med Res Rev, 35 (2015), pp. 126-151
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