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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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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. |
format | Online Article Text |
id | pubmed-6930976 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
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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