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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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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. |
format | Text |
id | pubmed-2222242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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