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A direct comparison of mouse and human intestinal development using epithelial gene expression patterns

PURPOSE: Preterm infants are susceptible to unique pathology due to their immaturity. Mouse models are commonly used to study immature intestinal disease including necrotizing enterocolitis (NEC). Current NEC models are performed at a variety of ages, but data directly comparing intestinal developme...

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Autores principales: Stanford, Amy H., Gong, Huiyu, Noonan, Mackenzie, Lewis, Angela N., Gong, Qingqing, Lanik, Wyatt E., Hsieh, Jonathan J., Lueschow, Shiloh R., Frey, Mark R., Good, Misty, McElroy, Steven J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930976/
https://www.ncbi.nlm.nih.gov/pubmed/31242501
http://dx.doi.org/10.1038/s41390-019-0472-y
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author Stanford, Amy H.
Gong, Huiyu
Noonan, Mackenzie
Lewis, Angela N.
Gong, Qingqing
Lanik, Wyatt E.
Hsieh, Jonathan J.
Lueschow, Shiloh R.
Frey, Mark R.
Good, Misty
McElroy, Steven J.
author_facet Stanford, Amy H.
Gong, Huiyu
Noonan, Mackenzie
Lewis, Angela N.
Gong, Qingqing
Lanik, Wyatt E.
Hsieh, Jonathan J.
Lueschow, Shiloh R.
Frey, Mark R.
Good, Misty
McElroy, Steven J.
author_sort Stanford, Amy H.
collection PubMed
description PURPOSE: Preterm infants are susceptible to unique pathology due to their immaturity. Mouse models are commonly used to study immature intestinal disease including necrotizing enterocolitis (NEC). Current NEC models are performed at a variety of ages, but data directly comparing intestinal developmental stage equivalency between mice and humans are lacking. METHODS: Small intestines were harvested from C57B1/6 mice at 3–4-day intervals from birth to P28 (n=8 at each age). Preterm human small intestine samples representing 17–23 weeks of completed gestation were obtained from the University of Pittsburgh Health Sciences Tissue Bank, and at term gestation during reanastamoses after resection for NEC (n=4–7 at each age). Quantification of intestinal epithelial cell types and mRNA for marker genes were evaluated on both species. RESULTS: Overall, murine and human developmental trends over time are markedly similar. Murine intestine prior to P10 is most similar to human fetal intestine prior to viability. Murine intestine at P14 is most similar to human intestine at 22–23 weeks completed gestation, and P28 murine intestine is most similar to human term intestine. CONCLUSION: Use of C57BL/6J mice to model the human immature intestine is reasonable, but the age of mouse chosen is a critical factor in model development.
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spelling pubmed-69309762019-12-27 A direct comparison of mouse and human intestinal development using epithelial gene expression patterns Stanford, Amy H. Gong, Huiyu Noonan, Mackenzie Lewis, Angela N. Gong, Qingqing Lanik, Wyatt E. Hsieh, Jonathan J. Lueschow, Shiloh R. Frey, Mark R. Good, Misty McElroy, Steven J. Pediatr Res Article PURPOSE: Preterm infants are susceptible to unique pathology due to their immaturity. Mouse models are commonly used to study immature intestinal disease including necrotizing enterocolitis (NEC). Current NEC models are performed at a variety of ages, but data directly comparing intestinal developmental stage equivalency between mice and humans are lacking. METHODS: Small intestines were harvested from C57B1/6 mice at 3–4-day intervals from birth to P28 (n=8 at each age). Preterm human small intestine samples representing 17–23 weeks of completed gestation were obtained from the University of Pittsburgh Health Sciences Tissue Bank, and at term gestation during reanastamoses after resection for NEC (n=4–7 at each age). Quantification of intestinal epithelial cell types and mRNA for marker genes were evaluated on both species. RESULTS: Overall, murine and human developmental trends over time are markedly similar. Murine intestine prior to P10 is most similar to human fetal intestine prior to viability. Murine intestine at P14 is most similar to human intestine at 22–23 weeks completed gestation, and P28 murine intestine is most similar to human term intestine. CONCLUSION: Use of C57BL/6J mice to model the human immature intestine is reasonable, but the age of mouse chosen is a critical factor in model development. 2019-06-26 2020-07 /pmc/articles/PMC6930976/ /pubmed/31242501 http://dx.doi.org/10.1038/s41390-019-0472-y Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Stanford, Amy H.
Gong, Huiyu
Noonan, Mackenzie
Lewis, Angela N.
Gong, Qingqing
Lanik, Wyatt E.
Hsieh, Jonathan J.
Lueschow, Shiloh R.
Frey, Mark R.
Good, Misty
McElroy, Steven J.
A direct comparison of mouse and human intestinal development using epithelial gene expression patterns
title A direct comparison of mouse and human intestinal development using epithelial gene expression patterns
title_full A direct comparison of mouse and human intestinal development using epithelial gene expression patterns
title_fullStr A direct comparison of mouse and human intestinal development using epithelial gene expression patterns
title_full_unstemmed A direct comparison of mouse and human intestinal development using epithelial gene expression patterns
title_short A direct comparison of mouse and human intestinal development using epithelial gene expression patterns
title_sort direct comparison of mouse and human intestinal development using epithelial gene expression patterns
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930976/
https://www.ncbi.nlm.nih.gov/pubmed/31242501
http://dx.doi.org/10.1038/s41390-019-0472-y
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