Gene expression analysis of the IPEC-J2 cell line: A simple model for the inflammation-sensitive preterm intestine

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Gene expression analysis of the IPEC-J2 cell line : A simple model for the inflammation-sensitive preterm intestine. / Støy, Ann Cathrine Findal; Heegaard, Peter M. H.; Sangild, Per Torp; Østergaard, Mette Viberg; Skovgaard, Kerstin.

I: ISRN Genomics, Bind 2013, 980651, 2013.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Støy, ACF, Heegaard, PMH, Sangild, PT, Østergaard, MV & Skovgaard, K 2013, 'Gene expression analysis of the IPEC-J2 cell line: A simple model for the inflammation-sensitive preterm intestine', ISRN Genomics, bind 2013, 980651. https://doi.org/10.1155/2013/980651

APA

Støy, A. C. F., Heegaard, P. M. H., Sangild, P. T., Østergaard, M. V., & Skovgaard, K. (2013). Gene expression analysis of the IPEC-J2 cell line: A simple model for the inflammation-sensitive preterm intestine. ISRN Genomics, 2013, [980651]. https://doi.org/10.1155/2013/980651

Vancouver

Støy ACF, Heegaard PMH, Sangild PT, Østergaard MV, Skovgaard K. Gene expression analysis of the IPEC-J2 cell line: A simple model for the inflammation-sensitive preterm intestine. ISRN Genomics. 2013;2013. 980651. https://doi.org/10.1155/2013/980651

Author

Støy, Ann Cathrine Findal ; Heegaard, Peter M. H. ; Sangild, Per Torp ; Østergaard, Mette Viberg ; Skovgaard, Kerstin. / Gene expression analysis of the IPEC-J2 cell line : A simple model for the inflammation-sensitive preterm intestine. I: ISRN Genomics. 2013 ; Bind 2013.

Bibtex

@article{93b42e826cbd4cebaf87c6bf2bdaeabe,
title = "Gene expression analysis of the IPEC-J2 cell line: A simple model for the inflammation-sensitive preterm intestine",
abstract = "The IPEC-J2 cell line was studied as a simple model for investigating responses of the newborn intestinal epithelium to diets. Especially, the small intestine of immature newborns is sensitive to diet-induced inflammation. We investigated gene expression of epithelial- and immune response-related genes in IPEC-J2 cells stimulated for 2 h with milk formula (CELL-FORM), colostrum (CELL-COLOS), or growth medium (CELL-CONTR) and in distal small intestinal tissue samples from preterm pigs fed milk formula (PIG-FORM) or colostrum (PIG-COLOS). High throughput quantitative PCR analysis of 48 genes revealed the expression of 22 genes in IPEC-J2 cells and 31 genes in intestinal samples. Principal component analysis (PCA) discriminated the gene expression profile of IPEC-J2 cells from that of intestinal samples. The expression profile of intestinal tissue was separated by PCA into 2 groups according to diet, whereas no diet-dependent grouping was seen for IPEC-J2 cells. Expression differences between PIG-FORM and PIG-COLOS were found for DEFB1, CXCL10, IL1RN, andALPI, while IL8was upregulated in CELL-FORM compared with CELL-CONTR. These differences, between IPEC-J2 cells and intestinal tissue from preterm pigs, both used as models for the newborn intestine, underline that caution must be exercised prior to analysis and interpretation of diet-induced effects on gene expression.",
author = "St{\o}y, {Ann Cathrine Findal} and Heegaard, {Peter M. H.} and Sangild, {Per Torp} and {\O}stergaard, {Mette Viberg} and Kerstin Skovgaard",
note = "CURIS 2013 NEXS 171",
year = "2013",
doi = "10.1155/2013/980651",
language = "English",
volume = "2013",
journal = "International Scholarly Research Notices",
issn = "2090-4452",
publisher = "Hindawi Publishing Corporation",

}

RIS

TY - JOUR

T1 - Gene expression analysis of the IPEC-J2 cell line

T2 - A simple model for the inflammation-sensitive preterm intestine

AU - Støy, Ann Cathrine Findal

AU - Heegaard, Peter M. H.

AU - Sangild, Per Torp

AU - Østergaard, Mette Viberg

AU - Skovgaard, Kerstin

N1 - CURIS 2013 NEXS 171

PY - 2013

Y1 - 2013

N2 - The IPEC-J2 cell line was studied as a simple model for investigating responses of the newborn intestinal epithelium to diets. Especially, the small intestine of immature newborns is sensitive to diet-induced inflammation. We investigated gene expression of epithelial- and immune response-related genes in IPEC-J2 cells stimulated for 2 h with milk formula (CELL-FORM), colostrum (CELL-COLOS), or growth medium (CELL-CONTR) and in distal small intestinal tissue samples from preterm pigs fed milk formula (PIG-FORM) or colostrum (PIG-COLOS). High throughput quantitative PCR analysis of 48 genes revealed the expression of 22 genes in IPEC-J2 cells and 31 genes in intestinal samples. Principal component analysis (PCA) discriminated the gene expression profile of IPEC-J2 cells from that of intestinal samples. The expression profile of intestinal tissue was separated by PCA into 2 groups according to diet, whereas no diet-dependent grouping was seen for IPEC-J2 cells. Expression differences between PIG-FORM and PIG-COLOS were found for DEFB1, CXCL10, IL1RN, andALPI, while IL8was upregulated in CELL-FORM compared with CELL-CONTR. These differences, between IPEC-J2 cells and intestinal tissue from preterm pigs, both used as models for the newborn intestine, underline that caution must be exercised prior to analysis and interpretation of diet-induced effects on gene expression.

AB - The IPEC-J2 cell line was studied as a simple model for investigating responses of the newborn intestinal epithelium to diets. Especially, the small intestine of immature newborns is sensitive to diet-induced inflammation. We investigated gene expression of epithelial- and immune response-related genes in IPEC-J2 cells stimulated for 2 h with milk formula (CELL-FORM), colostrum (CELL-COLOS), or growth medium (CELL-CONTR) and in distal small intestinal tissue samples from preterm pigs fed milk formula (PIG-FORM) or colostrum (PIG-COLOS). High throughput quantitative PCR analysis of 48 genes revealed the expression of 22 genes in IPEC-J2 cells and 31 genes in intestinal samples. Principal component analysis (PCA) discriminated the gene expression profile of IPEC-J2 cells from that of intestinal samples. The expression profile of intestinal tissue was separated by PCA into 2 groups according to diet, whereas no diet-dependent grouping was seen for IPEC-J2 cells. Expression differences between PIG-FORM and PIG-COLOS were found for DEFB1, CXCL10, IL1RN, andALPI, while IL8was upregulated in CELL-FORM compared with CELL-CONTR. These differences, between IPEC-J2 cells and intestinal tissue from preterm pigs, both used as models for the newborn intestine, underline that caution must be exercised prior to analysis and interpretation of diet-induced effects on gene expression.

U2 - 10.1155/2013/980651

DO - 10.1155/2013/980651

M3 - Journal article

VL - 2013

JO - International Scholarly Research Notices

JF - International Scholarly Research Notices

SN - 2090-4452

M1 - 980651

ER -

ID: 47523542