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Protein profiles of enzymatically isolated rumen epithelium in sheep fed a fibrous diet

BACKGROUND: The rumen wall plays a major role in efficient transfer of digested nutrients in the rumen to peripheral tissues through the portal venous system. Some of these substrates are metabolised in the epithelium during this process. To identify the specific proteins involved in these processes...

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Autores principales: Bond, J. J., Donaldson, A. J., Coumans, J. V. F., Austin, K., Ebert, D., Wheeler, D., Oddy, V. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346531/
https://www.ncbi.nlm.nih.gov/pubmed/30697422
http://dx.doi.org/10.1186/s40104-019-0314-0
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author Bond, J. J.
Donaldson, A. J.
Coumans, J. V. F.
Austin, K.
Ebert, D.
Wheeler, D.
Oddy, V. H.
author_facet Bond, J. J.
Donaldson, A. J.
Coumans, J. V. F.
Austin, K.
Ebert, D.
Wheeler, D.
Oddy, V. H.
author_sort Bond, J. J.
collection PubMed
description BACKGROUND: The rumen wall plays a major role in efficient transfer of digested nutrients in the rumen to peripheral tissues through the portal venous system. Some of these substrates are metabolised in the epithelium during this process. To identify the specific proteins involved in these processes, we used proteomic technologies. Protein extracts were prepared from ventral rumen tissue of six sheep fed a fibrous diet at 1.5× maintenance energy requirements. Using a newly developed method, we were able to enzymatically isolate the epithelial cells from underlying tissue layers, thus allowing cytosol and membrane fractions to be independently analysed using liquid chromatography tandem mass spectrometry (LC MS/MS). RESULTS: Using our procedure we identified 570 epithelial proteins in the Ovis aries sequence database. Subcellular locations were largely cytosolic (n = 221) and extracellular (n = 85). However, a quarter of the proteins identified were assigned to the plasma membrane or organelle membranes, some of which transport nutrients and metabolites. Of these 91 were transmembrane proteins (TMHMM), 27 had an N-terminal signal peptide (signalP) and TMHMM motif, 13 had a glycosylphosphatidylinositol (GPI) anchor and signalP sequence, 67 had beta (β) strands or 17 β strands and a transit peptide sequence, indicating the identified proteins were integral or peripheral membrane proteins. Subunits of the 5 protein complexes involved in mitochondrial cellular energy production were well represented. Structural proteins (15%), proteins involved in the metabolism of lipids and proteins (26%) and those with steroid or cytokine action were a feature of the proteome. CONCLUSION: Our research has developed a procedure to isolate rumen epithelium proteins from the underlying tissue layers so that they may be profiled using proteomic technologies. The approach improves the number of proteins that can be profiled that are specific to the epithelium of the rumen wall. It provides new insights into the proteins of structural and nutritional importance in the rumen epithelium, that carry out nutrient transport and metabolism, cell growth and signalling. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40104-019-0314-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-63465312019-01-29 Protein profiles of enzymatically isolated rumen epithelium in sheep fed a fibrous diet Bond, J. J. Donaldson, A. J. Coumans, J. V. F. Austin, K. Ebert, D. Wheeler, D. Oddy, V. H. J Anim Sci Biotechnol Research BACKGROUND: The rumen wall plays a major role in efficient transfer of digested nutrients in the rumen to peripheral tissues through the portal venous system. Some of these substrates are metabolised in the epithelium during this process. To identify the specific proteins involved in these processes, we used proteomic technologies. Protein extracts were prepared from ventral rumen tissue of six sheep fed a fibrous diet at 1.5× maintenance energy requirements. Using a newly developed method, we were able to enzymatically isolate the epithelial cells from underlying tissue layers, thus allowing cytosol and membrane fractions to be independently analysed using liquid chromatography tandem mass spectrometry (LC MS/MS). RESULTS: Using our procedure we identified 570 epithelial proteins in the Ovis aries sequence database. Subcellular locations were largely cytosolic (n = 221) and extracellular (n = 85). However, a quarter of the proteins identified were assigned to the plasma membrane or organelle membranes, some of which transport nutrients and metabolites. Of these 91 were transmembrane proteins (TMHMM), 27 had an N-terminal signal peptide (signalP) and TMHMM motif, 13 had a glycosylphosphatidylinositol (GPI) anchor and signalP sequence, 67 had beta (β) strands or 17 β strands and a transit peptide sequence, indicating the identified proteins were integral or peripheral membrane proteins. Subunits of the 5 protein complexes involved in mitochondrial cellular energy production were well represented. Structural proteins (15%), proteins involved in the metabolism of lipids and proteins (26%) and those with steroid or cytokine action were a feature of the proteome. CONCLUSION: Our research has developed a procedure to isolate rumen epithelium proteins from the underlying tissue layers so that they may be profiled using proteomic technologies. The approach improves the number of proteins that can be profiled that are specific to the epithelium of the rumen wall. It provides new insights into the proteins of structural and nutritional importance in the rumen epithelium, that carry out nutrient transport and metabolism, cell growth and signalling. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40104-019-0314-0) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-25 /pmc/articles/PMC6346531/ /pubmed/30697422 http://dx.doi.org/10.1186/s40104-019-0314-0 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Bond, J. J.
Donaldson, A. J.
Coumans, J. V. F.
Austin, K.
Ebert, D.
Wheeler, D.
Oddy, V. H.
Protein profiles of enzymatically isolated rumen epithelium in sheep fed a fibrous diet
title Protein profiles of enzymatically isolated rumen epithelium in sheep fed a fibrous diet
title_full Protein profiles of enzymatically isolated rumen epithelium in sheep fed a fibrous diet
title_fullStr Protein profiles of enzymatically isolated rumen epithelium in sheep fed a fibrous diet
title_full_unstemmed Protein profiles of enzymatically isolated rumen epithelium in sheep fed a fibrous diet
title_short Protein profiles of enzymatically isolated rumen epithelium in sheep fed a fibrous diet
title_sort protein profiles of enzymatically isolated rumen epithelium in sheep fed a fibrous diet
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346531/
https://www.ncbi.nlm.nih.gov/pubmed/30697422
http://dx.doi.org/10.1186/s40104-019-0314-0
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