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Lung branching morphogenesis is accompanied by temporal metabolic changes towards a glycolytic preference

BACKGROUND: Lung branching morphogenesis is characterized by epithelial-mesenchymal interactions that ultimately define the airway conducting system. Throughout this process, energy and structural macromolecules are necessary to sustain the high proliferative rates. The extensive knowledge of the mo...

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Autores principales: Fernandes-Silva, Hugo, Alves, Marco G., Araújo-Silva, Henrique, Silva, Ana M., Correia-Pinto, Jorge, Oliveira, Pedro F., Moura, Rute S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285861/
https://www.ncbi.nlm.nih.gov/pubmed/34274010
http://dx.doi.org/10.1186/s13578-021-00654-w
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author Fernandes-Silva, Hugo
Alves, Marco G.
Araújo-Silva, Henrique
Silva, Ana M.
Correia-Pinto, Jorge
Oliveira, Pedro F.
Moura, Rute S.
author_facet Fernandes-Silva, Hugo
Alves, Marco G.
Araújo-Silva, Henrique
Silva, Ana M.
Correia-Pinto, Jorge
Oliveira, Pedro F.
Moura, Rute S.
author_sort Fernandes-Silva, Hugo
collection PubMed
description BACKGROUND: Lung branching morphogenesis is characterized by epithelial-mesenchymal interactions that ultimately define the airway conducting system. Throughout this process, energy and structural macromolecules are necessary to sustain the high proliferative rates. The extensive knowledge of the molecular mechanisms underlying pulmonary development contrasts with the lack of data regarding the embryonic lung metabolic requirements. Here, we studied the metabolic profile associated with the early stages of chicken pulmonary branching. METHODS: In this study, we used an ex vivo lung explant culture system and analyzed the consumption/production of extracellular metabolic intermediates associated with glucose catabolism (alanine, lactate, and acetate) by (1)H-NMR spectroscopy in the culture medium. Then, we characterized the transcript levels of metabolite membrane transporters (glut1, glut3, glut8, mct1, mct3, mct4, and mct8) and glycolytic enzymes (hk1, hk2, pfk1, ldha, ldhb, pdha, and pdhb) by qPCR. ldha and ldhb mRNA spatial localization was determined by in situ hybridization. Proliferation was analyzed by directly assessing DNA synthesis using an EdU-based assay. Additionally, we performed western blot to analyze LDHA and LDHT protein levels. Finally, we used a Clark-Type Electrode to assess the lung explant's respiratory capacity. RESULTS: Glucose consumption decreases, whereas alanine, lactate, and acetate production progressively increase as branching morphogenesis proceeds. mRNA analysis revealed variations in the expression levels of key enzymes and transporters from the glycolytic pathway. ldha and ldhb displayed a compartment-specific expression pattern that resembles proximal–distal markers. In addition, high proliferation levels were detected at active branching sites. LDH protein expression levels suggest that LDHB may account for the progressive rise in lactate. Concurrently, there is a stable oxygen consumption rate throughout branching morphogenesis. CONCLUSIONS: This report describes the temporal metabolic changes that accompany the early stages of chicken lung branching morphogenesis. Overall, the embryonic chicken lung seems to shift to a glycolytic lactate-based metabolism as pulmonary branching occurs. Moreover, this metabolic rewiring might play a crucial role during lung development. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13578-021-00654-w.
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spelling pubmed-82858612021-07-19 Lung branching morphogenesis is accompanied by temporal metabolic changes towards a glycolytic preference Fernandes-Silva, Hugo Alves, Marco G. Araújo-Silva, Henrique Silva, Ana M. Correia-Pinto, Jorge Oliveira, Pedro F. Moura, Rute S. Cell Biosci Research BACKGROUND: Lung branching morphogenesis is characterized by epithelial-mesenchymal interactions that ultimately define the airway conducting system. Throughout this process, energy and structural macromolecules are necessary to sustain the high proliferative rates. The extensive knowledge of the molecular mechanisms underlying pulmonary development contrasts with the lack of data regarding the embryonic lung metabolic requirements. Here, we studied the metabolic profile associated with the early stages of chicken pulmonary branching. METHODS: In this study, we used an ex vivo lung explant culture system and analyzed the consumption/production of extracellular metabolic intermediates associated with glucose catabolism (alanine, lactate, and acetate) by (1)H-NMR spectroscopy in the culture medium. Then, we characterized the transcript levels of metabolite membrane transporters (glut1, glut3, glut8, mct1, mct3, mct4, and mct8) and glycolytic enzymes (hk1, hk2, pfk1, ldha, ldhb, pdha, and pdhb) by qPCR. ldha and ldhb mRNA spatial localization was determined by in situ hybridization. Proliferation was analyzed by directly assessing DNA synthesis using an EdU-based assay. Additionally, we performed western blot to analyze LDHA and LDHT protein levels. Finally, we used a Clark-Type Electrode to assess the lung explant's respiratory capacity. RESULTS: Glucose consumption decreases, whereas alanine, lactate, and acetate production progressively increase as branching morphogenesis proceeds. mRNA analysis revealed variations in the expression levels of key enzymes and transporters from the glycolytic pathway. ldha and ldhb displayed a compartment-specific expression pattern that resembles proximal–distal markers. In addition, high proliferation levels were detected at active branching sites. LDH protein expression levels suggest that LDHB may account for the progressive rise in lactate. Concurrently, there is a stable oxygen consumption rate throughout branching morphogenesis. CONCLUSIONS: This report describes the temporal metabolic changes that accompany the early stages of chicken lung branching morphogenesis. Overall, the embryonic chicken lung seems to shift to a glycolytic lactate-based metabolism as pulmonary branching occurs. Moreover, this metabolic rewiring might play a crucial role during lung development. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13578-021-00654-w. BioMed Central 2021-07-17 /pmc/articles/PMC8285861/ /pubmed/34274010 http://dx.doi.org/10.1186/s13578-021-00654-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Fernandes-Silva, Hugo
Alves, Marco G.
Araújo-Silva, Henrique
Silva, Ana M.
Correia-Pinto, Jorge
Oliveira, Pedro F.
Moura, Rute S.
Lung branching morphogenesis is accompanied by temporal metabolic changes towards a glycolytic preference
title Lung branching morphogenesis is accompanied by temporal metabolic changes towards a glycolytic preference
title_full Lung branching morphogenesis is accompanied by temporal metabolic changes towards a glycolytic preference
title_fullStr Lung branching morphogenesis is accompanied by temporal metabolic changes towards a glycolytic preference
title_full_unstemmed Lung branching morphogenesis is accompanied by temporal metabolic changes towards a glycolytic preference
title_short Lung branching morphogenesis is accompanied by temporal metabolic changes towards a glycolytic preference
title_sort lung branching morphogenesis is accompanied by temporal metabolic changes towards a glycolytic preference
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285861/
https://www.ncbi.nlm.nih.gov/pubmed/34274010
http://dx.doi.org/10.1186/s13578-021-00654-w
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