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Differential gene expression profile in the small intestines of mice lacking pacemaker interstitial cells of Cajal

BACKGROUND: We previously identified eight known and novel genes differentially expressed in the small intestines of wild type and W/W(V )mice, which have greatly reduced populations of the interstitial cells of Cajal, that are responsible for the generation of electrical slow waves, by using a diff...

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Autores principales: Daigo, Yataro, Takayama, Ichiro, Ponder, Bruce AJ, Caldas, Carlos, Ward, Sean M, Sanders, Kenton M, Fujino, Masayuki A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC198276/
https://www.ncbi.nlm.nih.gov/pubmed/12831403
http://dx.doi.org/10.1186/1471-230X-3-17
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author Daigo, Yataro
Takayama, Ichiro
Ponder, Bruce AJ
Caldas, Carlos
Ward, Sean M
Sanders, Kenton M
Fujino, Masayuki A
author_facet Daigo, Yataro
Takayama, Ichiro
Ponder, Bruce AJ
Caldas, Carlos
Ward, Sean M
Sanders, Kenton M
Fujino, Masayuki A
author_sort Daigo, Yataro
collection PubMed
description BACKGROUND: We previously identified eight known and novel genes differentially expressed in the small intestines of wild type and W/W(V )mice, which have greatly reduced populations of the interstitial cells of Cajal, that are responsible for the generation of electrical slow waves, by using a differential gene display method. METHODS: By using the same method we isolated additional candidate genes that were specifically down- or up-regulated in W/W(V )mice. Novel transcripts were designated as DDWMEST. RESULTS: We isolated seven candidates that were specifically down- or up-regulated in W/W(V )mice. Two novel transcripts, DDWMEST 1 and -91 were increased in both fed and fasted W/W(V )mice. Expression of another five genes was suppressed in W/W(V )mice: ARG2 (Arginase II), ONZIN (encoding leukemia inhibitory factor regulated protein), and three novel transcripts: DDWMEST62, -84, and -100. Together with the previous report, we identified fifteen differentially expressed genes in total in the small intestines of W/W(V )mice. Eight of these genes were reduced in the jejunums of W/W(V )mice compared to age matched wild type mice, whereas the other seven genes showed an increase in expression. Differential expression was the same in fasted and fed animals, suggesting that the differences were independent of the dietetic state of the animal. CONCLUSIONS: Several known and novel genes are differentially expressed in the small intestines of W/W(V )mice. Differential gene comparison might contribute to our understanding of motility disorders associated with the loss of the interstitial cells of Cajal.
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spelling pubmed-1982762003-09-25 Differential gene expression profile in the small intestines of mice lacking pacemaker interstitial cells of Cajal Daigo, Yataro Takayama, Ichiro Ponder, Bruce AJ Caldas, Carlos Ward, Sean M Sanders, Kenton M Fujino, Masayuki A BMC Gastroenterol Research Article BACKGROUND: We previously identified eight known and novel genes differentially expressed in the small intestines of wild type and W/W(V )mice, which have greatly reduced populations of the interstitial cells of Cajal, that are responsible for the generation of electrical slow waves, by using a differential gene display method. METHODS: By using the same method we isolated additional candidate genes that were specifically down- or up-regulated in W/W(V )mice. Novel transcripts were designated as DDWMEST. RESULTS: We isolated seven candidates that were specifically down- or up-regulated in W/W(V )mice. Two novel transcripts, DDWMEST 1 and -91 were increased in both fed and fasted W/W(V )mice. Expression of another five genes was suppressed in W/W(V )mice: ARG2 (Arginase II), ONZIN (encoding leukemia inhibitory factor regulated protein), and three novel transcripts: DDWMEST62, -84, and -100. Together with the previous report, we identified fifteen differentially expressed genes in total in the small intestines of W/W(V )mice. Eight of these genes were reduced in the jejunums of W/W(V )mice compared to age matched wild type mice, whereas the other seven genes showed an increase in expression. Differential expression was the same in fasted and fed animals, suggesting that the differences were independent of the dietetic state of the animal. CONCLUSIONS: Several known and novel genes are differentially expressed in the small intestines of W/W(V )mice. Differential gene comparison might contribute to our understanding of motility disorders associated with the loss of the interstitial cells of Cajal. BioMed Central 2003-06-29 /pmc/articles/PMC198276/ /pubmed/12831403 http://dx.doi.org/10.1186/1471-230X-3-17 Text en Copyright © 2003 Daigo et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
Daigo, Yataro
Takayama, Ichiro
Ponder, Bruce AJ
Caldas, Carlos
Ward, Sean M
Sanders, Kenton M
Fujino, Masayuki A
Differential gene expression profile in the small intestines of mice lacking pacemaker interstitial cells of Cajal
title Differential gene expression profile in the small intestines of mice lacking pacemaker interstitial cells of Cajal
title_full Differential gene expression profile in the small intestines of mice lacking pacemaker interstitial cells of Cajal
title_fullStr Differential gene expression profile in the small intestines of mice lacking pacemaker interstitial cells of Cajal
title_full_unstemmed Differential gene expression profile in the small intestines of mice lacking pacemaker interstitial cells of Cajal
title_short Differential gene expression profile in the small intestines of mice lacking pacemaker interstitial cells of Cajal
title_sort differential gene expression profile in the small intestines of mice lacking pacemaker interstitial cells of cajal
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC198276/
https://www.ncbi.nlm.nih.gov/pubmed/12831403
http://dx.doi.org/10.1186/1471-230X-3-17
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