Postnatal Hematopoiesis and Gut Microbiota in NOD Mice Deviate from C57BL/6 Mice

Neonatal studies in different mouse strains reveal that early life colonization affects the development of adaptive immunity in mice. The nonobese diabetic (NOD) mouse spontaneously develops autoimmune diabetes, but neonatal studies of NOD mice are lacking. We hypothesized that NOD mice deviate from...

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Main Authors: Dina Silke Malling Damlund, Stine Broeng Metzdorff, Jane Preuss Hasselby, Maria Wiese, Mia Lundsager, Dennis Sandris Nielsen, Karsten Stig Buschard, Axel Kornerup Hansen, Hanne Frøkiær
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Journal of Diabetes Research
Online Access:http://dx.doi.org/10.1155/2016/6321980
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author Dina Silke Malling Damlund
Stine Broeng Metzdorff
Jane Preuss Hasselby
Maria Wiese
Mia Lundsager
Dennis Sandris Nielsen
Karsten Stig Buschard
Axel Kornerup Hansen
Hanne Frøkiær
author_facet Dina Silke Malling Damlund
Stine Broeng Metzdorff
Jane Preuss Hasselby
Maria Wiese
Mia Lundsager
Dennis Sandris Nielsen
Karsten Stig Buschard
Axel Kornerup Hansen
Hanne Frøkiær
author_sort Dina Silke Malling Damlund
collection DOAJ
description Neonatal studies in different mouse strains reveal that early life colonization affects the development of adaptive immunity in mice. The nonobese diabetic (NOD) mouse spontaneously develops autoimmune diabetes, but neonatal studies of NOD mice are lacking. We hypothesized that NOD mice deviate from another much used mouse strain, C57BL/6, with respect to postnatal microbiota and/or hematopoiesis and compared this in newborn mice of dams housed under the same conditions. A distinct bacteria profile rich in staphylococci was found at postnatal days (PND) 1–4 in NOD mice. Furthermore, a distinct splenic cell profile high in a granulocytic phenotype was evident in the neonatal NOD mice whereas neonatal C57BL/6 mice showed a profile rich in monocytes. Neonatal expression of Reg3g and Muc2 in the gut was deviating in NOD mice and coincided with fewer bacteria attaching to the Mucosal surface in NOD compared to C57BL/6 mice.
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series Journal of Diabetes Research
spelling doaj-art-afc9ee67a0b74f4ebf7cd4e6006851512025-02-03T01:27:54ZengWileyJournal of Diabetes Research2314-67452314-67532016-01-01201610.1155/2016/63219806321980Postnatal Hematopoiesis and Gut Microbiota in NOD Mice Deviate from C57BL/6 MiceDina Silke Malling Damlund0Stine Broeng Metzdorff1Jane Preuss Hasselby2Maria Wiese3Mia Lundsager4Dennis Sandris Nielsen5Karsten Stig Buschard6Axel Kornerup Hansen7Hanne Frøkiær8Department of Veterinary Disease Biology, Faculty of Health and Medical Sciences, University of Copenhagen, 1870 Frederiksberg C, DenmarkDepartment of Veterinary Disease Biology, Faculty of Health and Medical Sciences, University of Copenhagen, 1870 Frederiksberg C, DenmarkDepartment of Pathology, Rigshospitalet, 2100 Copenhagen, DenmarkDepartment of Food Science, University of Copenhagen, 1870 Frederiksberg C, DenmarkDepartment of Veterinary Disease Biology, Faculty of Health and Medical Sciences, University of Copenhagen, 1870 Frederiksberg C, DenmarkDepartment of Food Science, University of Copenhagen, 1870 Frederiksberg C, DenmarkBartholin Institute, Rigshospitalet, 2100 Copenhagen, DenmarkDepartment of Veterinary Disease Biology, Faculty of Health and Medical Sciences, University of Copenhagen, 1870 Frederiksberg C, DenmarkDepartment of Veterinary Disease Biology, Faculty of Health and Medical Sciences, University of Copenhagen, 1870 Frederiksberg C, DenmarkNeonatal studies in different mouse strains reveal that early life colonization affects the development of adaptive immunity in mice. The nonobese diabetic (NOD) mouse spontaneously develops autoimmune diabetes, but neonatal studies of NOD mice are lacking. We hypothesized that NOD mice deviate from another much used mouse strain, C57BL/6, with respect to postnatal microbiota and/or hematopoiesis and compared this in newborn mice of dams housed under the same conditions. A distinct bacteria profile rich in staphylococci was found at postnatal days (PND) 1–4 in NOD mice. Furthermore, a distinct splenic cell profile high in a granulocytic phenotype was evident in the neonatal NOD mice whereas neonatal C57BL/6 mice showed a profile rich in monocytes. Neonatal expression of Reg3g and Muc2 in the gut was deviating in NOD mice and coincided with fewer bacteria attaching to the Mucosal surface in NOD compared to C57BL/6 mice.http://dx.doi.org/10.1155/2016/6321980
spellingShingle Dina Silke Malling Damlund
Stine Broeng Metzdorff
Jane Preuss Hasselby
Maria Wiese
Mia Lundsager
Dennis Sandris Nielsen
Karsten Stig Buschard
Axel Kornerup Hansen
Hanne Frøkiær
Postnatal Hematopoiesis and Gut Microbiota in NOD Mice Deviate from C57BL/6 Mice
Journal of Diabetes Research
title Postnatal Hematopoiesis and Gut Microbiota in NOD Mice Deviate from C57BL/6 Mice
title_full Postnatal Hematopoiesis and Gut Microbiota in NOD Mice Deviate from C57BL/6 Mice
title_fullStr Postnatal Hematopoiesis and Gut Microbiota in NOD Mice Deviate from C57BL/6 Mice
title_full_unstemmed Postnatal Hematopoiesis and Gut Microbiota in NOD Mice Deviate from C57BL/6 Mice
title_short Postnatal Hematopoiesis and Gut Microbiota in NOD Mice Deviate from C57BL/6 Mice
title_sort postnatal hematopoiesis and gut microbiota in nod mice deviate from c57bl 6 mice
url http://dx.doi.org/10.1155/2016/6321980
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