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Serum Immune-Related Proteins are Differentially Expressed during Hibernation in the American Black Bear

Hibernation is an adaptation to conserve energy in the face of extreme environmental conditions and low food availability that has risen in several animal phyla. This phenomenon is characterized by reduced metabolic rate (∼25% of the active basal metabolic rate in hibernating bears) and energy deman...

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Autores principales: Chow, Brian A., Donahue, Seth W., Vaughan, Michael R., McConkey, Brendan, Vijayan, Mathilakath M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3692520/
https://www.ncbi.nlm.nih.gov/pubmed/23825529
http://dx.doi.org/10.1371/journal.pone.0066119
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author Chow, Brian A.
Donahue, Seth W.
Vaughan, Michael R.
McConkey, Brendan
Vijayan, Mathilakath M.
author_facet Chow, Brian A.
Donahue, Seth W.
Vaughan, Michael R.
McConkey, Brendan
Vijayan, Mathilakath M.
author_sort Chow, Brian A.
collection PubMed
description Hibernation is an adaptation to conserve energy in the face of extreme environmental conditions and low food availability that has risen in several animal phyla. This phenomenon is characterized by reduced metabolic rate (∼25% of the active basal metabolic rate in hibernating bears) and energy demand, while other physiological adjustments are far from clear. The profiling of the serum proteome of the American black bear (Ursus americanus) may reveal specific proteins that are differentially modulated by hibernation, and provide insight into the remarkable physiological adaptations that characterize ursid hibernation. In this study, we used differential gel electrophoresis (DIGE) analysis, liquid chromatography coupled to tandem mass spectrometry, and subsequent MASCOT analysis of the mass spectra to identify candidate proteins that are differentially expressed during hibernation in captive black bears. Seventy serum proteins were identified as changing by ±1.5 fold or more, out of which 34 proteins increased expression during hibernation. The majority of identified proteins are involved in immune system processes. These included α(2)-macroglobulin, complement components C1s and C4, immunoglobulin μ and J chains, clusterin, haptoglobin, C4b binding protein, kininogen 1, α(2)-HS-glycoprotein, and apoplipoproteins A-I and A-IV. Differential expression of a subset of these proteins identified by proteomic analysis was also confirmed by immunodetection. We propose that the observed serum protein changes contribute to the maintenance of the hibernation phenotype and health, including increased capacities for bone maintenance and wound healing during hibernation in bears.
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spelling pubmed-36925202013-07-02 Serum Immune-Related Proteins are Differentially Expressed during Hibernation in the American Black Bear Chow, Brian A. Donahue, Seth W. Vaughan, Michael R. McConkey, Brendan Vijayan, Mathilakath M. PLoS One Research Article Hibernation is an adaptation to conserve energy in the face of extreme environmental conditions and low food availability that has risen in several animal phyla. This phenomenon is characterized by reduced metabolic rate (∼25% of the active basal metabolic rate in hibernating bears) and energy demand, while other physiological adjustments are far from clear. The profiling of the serum proteome of the American black bear (Ursus americanus) may reveal specific proteins that are differentially modulated by hibernation, and provide insight into the remarkable physiological adaptations that characterize ursid hibernation. In this study, we used differential gel electrophoresis (DIGE) analysis, liquid chromatography coupled to tandem mass spectrometry, and subsequent MASCOT analysis of the mass spectra to identify candidate proteins that are differentially expressed during hibernation in captive black bears. Seventy serum proteins were identified as changing by ±1.5 fold or more, out of which 34 proteins increased expression during hibernation. The majority of identified proteins are involved in immune system processes. These included α(2)-macroglobulin, complement components C1s and C4, immunoglobulin μ and J chains, clusterin, haptoglobin, C4b binding protein, kininogen 1, α(2)-HS-glycoprotein, and apoplipoproteins A-I and A-IV. Differential expression of a subset of these proteins identified by proteomic analysis was also confirmed by immunodetection. We propose that the observed serum protein changes contribute to the maintenance of the hibernation phenotype and health, including increased capacities for bone maintenance and wound healing during hibernation in bears. Public Library of Science 2013-06-25 /pmc/articles/PMC3692520/ /pubmed/23825529 http://dx.doi.org/10.1371/journal.pone.0066119 Text en © 2013 Chow et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chow, Brian A.
Donahue, Seth W.
Vaughan, Michael R.
McConkey, Brendan
Vijayan, Mathilakath M.
Serum Immune-Related Proteins are Differentially Expressed during Hibernation in the American Black Bear
title Serum Immune-Related Proteins are Differentially Expressed during Hibernation in the American Black Bear
title_full Serum Immune-Related Proteins are Differentially Expressed during Hibernation in the American Black Bear
title_fullStr Serum Immune-Related Proteins are Differentially Expressed during Hibernation in the American Black Bear
title_full_unstemmed Serum Immune-Related Proteins are Differentially Expressed during Hibernation in the American Black Bear
title_short Serum Immune-Related Proteins are Differentially Expressed during Hibernation in the American Black Bear
title_sort serum immune-related proteins are differentially expressed during hibernation in the american black bear
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3692520/
https://www.ncbi.nlm.nih.gov/pubmed/23825529
http://dx.doi.org/10.1371/journal.pone.0066119
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