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An extensive phenotypic characterization of the hTNFα transgenic mice

BACKGROUND: Tumor necrosis factor alpha (TNFα) is implicated in a wide variety of pathological and physiological processes, including chronic inflammatory conditions, coronary artery disease, diabetes, obesity, and cachexia. Transgenic mice expressing human TNFα (hTNFα) have previously been describe...

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Autores principales: Hayward, Michael D, Jones, Beverly K, Saparov, Arman, Hain, Heather S, Trillat, Anne-Cecile, Bunzel, Michelle M, Corona, Aaron, Li-Wang, Bifang, Strenkowski, Bryan, Giordano, Caroline, Shen, Hai, Arcamone, Emily, Weidlick, Jeffrey, Vilensky, Maria, Tugusheva, Marina, Felkner, Roland H, Campbell, William, Rao, Yu, Grass, David S, Buiakova, Olesia
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2222242/
https://www.ncbi.nlm.nih.gov/pubmed/18070349
http://dx.doi.org/10.1186/1472-6793-7-13
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author Hayward, Michael D
Jones, Beverly K
Saparov, Arman
Hain, Heather S
Trillat, Anne-Cecile
Bunzel, Michelle M
Corona, Aaron
Li-Wang, Bifang
Strenkowski, Bryan
Giordano, Caroline
Shen, Hai
Arcamone, Emily
Weidlick, Jeffrey
Vilensky, Maria
Tugusheva, Marina
Felkner, Roland H
Campbell, William
Rao, Yu
Grass, David S
Buiakova, Olesia
author_facet Hayward, Michael D
Jones, Beverly K
Saparov, Arman
Hain, Heather S
Trillat, Anne-Cecile
Bunzel, Michelle M
Corona, Aaron
Li-Wang, Bifang
Strenkowski, Bryan
Giordano, Caroline
Shen, Hai
Arcamone, Emily
Weidlick, Jeffrey
Vilensky, Maria
Tugusheva, Marina
Felkner, Roland H
Campbell, William
Rao, Yu
Grass, David S
Buiakova, Olesia
author_sort Hayward, Michael D
collection PubMed
description BACKGROUND: Tumor necrosis factor alpha (TNFα) is implicated in a wide variety of pathological and physiological processes, including chronic inflammatory conditions, coronary artery disease, diabetes, obesity, and cachexia. Transgenic mice expressing human TNFα (hTNFα) have previously been described as a model for progressive rheumatoid arthritis. In this report, we describe extensive characterization of an hTNFα transgenic mouse line. RESULTS: In addition to arthritis, these hTNFα transgenic mice demonstrated major alterations in body composition, metabolic rate, leptin levels, response to a high-fat diet, bone mineral density and content, impaired fertility and male sexual function. Many phenotypes displayed an earlier onset and a higher degree of severity in males, pointing towards a significant degree of sexual dimorphism in response to deregulated expression of TNFα. CONCLUSION: These results highlight the potential usefulness of this transgenic model as a resource for studying the progressive effects of constitutively expressed low levels of circulating TNFα, a condition mimicking that observed in a number of human pathological conditions.
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spelling pubmed-22222422008-02-01 An extensive phenotypic characterization of the hTNFα transgenic mice Hayward, Michael D Jones, Beverly K Saparov, Arman Hain, Heather S Trillat, Anne-Cecile Bunzel, Michelle M Corona, Aaron Li-Wang, Bifang Strenkowski, Bryan Giordano, Caroline Shen, Hai Arcamone, Emily Weidlick, Jeffrey Vilensky, Maria Tugusheva, Marina Felkner, Roland H Campbell, William Rao, Yu Grass, David S Buiakova, Olesia BMC Physiol Research Article BACKGROUND: Tumor necrosis factor alpha (TNFα) is implicated in a wide variety of pathological and physiological processes, including chronic inflammatory conditions, coronary artery disease, diabetes, obesity, and cachexia. Transgenic mice expressing human TNFα (hTNFα) have previously been described as a model for progressive rheumatoid arthritis. In this report, we describe extensive characterization of an hTNFα transgenic mouse line. RESULTS: In addition to arthritis, these hTNFα transgenic mice demonstrated major alterations in body composition, metabolic rate, leptin levels, response to a high-fat diet, bone mineral density and content, impaired fertility and male sexual function. Many phenotypes displayed an earlier onset and a higher degree of severity in males, pointing towards a significant degree of sexual dimorphism in response to deregulated expression of TNFα. CONCLUSION: These results highlight the potential usefulness of this transgenic model as a resource for studying the progressive effects of constitutively expressed low levels of circulating TNFα, a condition mimicking that observed in a number of human pathological conditions. BioMed Central 2007-12-10 /pmc/articles/PMC2222242/ /pubmed/18070349 http://dx.doi.org/10.1186/1472-6793-7-13 Text en Copyright © 2007 Hayward et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hayward, Michael D
Jones, Beverly K
Saparov, Arman
Hain, Heather S
Trillat, Anne-Cecile
Bunzel, Michelle M
Corona, Aaron
Li-Wang, Bifang
Strenkowski, Bryan
Giordano, Caroline
Shen, Hai
Arcamone, Emily
Weidlick, Jeffrey
Vilensky, Maria
Tugusheva, Marina
Felkner, Roland H
Campbell, William
Rao, Yu
Grass, David S
Buiakova, Olesia
An extensive phenotypic characterization of the hTNFα transgenic mice
title An extensive phenotypic characterization of the hTNFα transgenic mice
title_full An extensive phenotypic characterization of the hTNFα transgenic mice
title_fullStr An extensive phenotypic characterization of the hTNFα transgenic mice
title_full_unstemmed An extensive phenotypic characterization of the hTNFα transgenic mice
title_short An extensive phenotypic characterization of the hTNFα transgenic mice
title_sort extensive phenotypic characterization of the htnfα transgenic mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2222242/
https://www.ncbi.nlm.nih.gov/pubmed/18070349
http://dx.doi.org/10.1186/1472-6793-7-13
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