Cargando…
Maternal diet during early gestation influences postnatal taste activity–dependent pruning by microglia
A key process in central sensory circuit development involves activity-dependent pruning of exuberant terminals. Here, we studied gustatory terminal field maturation in the postnatal mouse nucleus of the solitary tract (NST) during normal development and in mice where their mothers were fed a low Na...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512853/ https://www.ncbi.nlm.nih.gov/pubmed/37733279 http://dx.doi.org/10.1084/jem.20212476 |
_version_ | 1785108448352927744 |
---|---|
author | Sun, Chengsan Zheng, Shuqiu Perry, Justin S.A. Norris, Geoffrey T. Cheng, Mei Kong, Fanzhen Skyberg, Rolf Cang, Jianhua Erisir, Alev Kipnis, Jonathan Hill, David L. |
author_facet | Sun, Chengsan Zheng, Shuqiu Perry, Justin S.A. Norris, Geoffrey T. Cheng, Mei Kong, Fanzhen Skyberg, Rolf Cang, Jianhua Erisir, Alev Kipnis, Jonathan Hill, David L. |
author_sort | Sun, Chengsan |
collection | PubMed |
description | A key process in central sensory circuit development involves activity-dependent pruning of exuberant terminals. Here, we studied gustatory terminal field maturation in the postnatal mouse nucleus of the solitary tract (NST) during normal development and in mice where their mothers were fed a low NaCl diet for a limited period soon after conception. Pruning of terminal fields of gustatory nerves in controls involved the complement system and is likely driven by NaCl-elicited taste activity. In contrast, offspring of mothers with an early dietary manipulation failed to prune gustatory terminal fields even though peripheral taste activity developed normally. The ability to prune in these mice was rescued by activating myeloid cells postnatally, and conversely, pruning was arrested in controls with the loss of myeloid cell function. The altered pruning and myeloid cell function appear to be programmed before the peripheral gustatory system is assembled and corresponds to the embryonic period when microglia progenitors derived from the yolk sac migrate to and colonize the brain. |
format | Online Article Text |
id | pubmed-10512853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-105128532023-09-22 Maternal diet during early gestation influences postnatal taste activity–dependent pruning by microglia Sun, Chengsan Zheng, Shuqiu Perry, Justin S.A. Norris, Geoffrey T. Cheng, Mei Kong, Fanzhen Skyberg, Rolf Cang, Jianhua Erisir, Alev Kipnis, Jonathan Hill, David L. J Exp Med Article A key process in central sensory circuit development involves activity-dependent pruning of exuberant terminals. Here, we studied gustatory terminal field maturation in the postnatal mouse nucleus of the solitary tract (NST) during normal development and in mice where their mothers were fed a low NaCl diet for a limited period soon after conception. Pruning of terminal fields of gustatory nerves in controls involved the complement system and is likely driven by NaCl-elicited taste activity. In contrast, offspring of mothers with an early dietary manipulation failed to prune gustatory terminal fields even though peripheral taste activity developed normally. The ability to prune in these mice was rescued by activating myeloid cells postnatally, and conversely, pruning was arrested in controls with the loss of myeloid cell function. The altered pruning and myeloid cell function appear to be programmed before the peripheral gustatory system is assembled and corresponds to the embryonic period when microglia progenitors derived from the yolk sac migrate to and colonize the brain. Rockefeller University Press 2023-09-21 /pmc/articles/PMC10512853/ /pubmed/37733279 http://dx.doi.org/10.1084/jem.20212476 Text en © 2023 Sun et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sun, Chengsan Zheng, Shuqiu Perry, Justin S.A. Norris, Geoffrey T. Cheng, Mei Kong, Fanzhen Skyberg, Rolf Cang, Jianhua Erisir, Alev Kipnis, Jonathan Hill, David L. Maternal diet during early gestation influences postnatal taste activity–dependent pruning by microglia |
title | Maternal diet during early gestation influences postnatal taste activity–dependent pruning by microglia |
title_full | Maternal diet during early gestation influences postnatal taste activity–dependent pruning by microglia |
title_fullStr | Maternal diet during early gestation influences postnatal taste activity–dependent pruning by microglia |
title_full_unstemmed | Maternal diet during early gestation influences postnatal taste activity–dependent pruning by microglia |
title_short | Maternal diet during early gestation influences postnatal taste activity–dependent pruning by microglia |
title_sort | maternal diet during early gestation influences postnatal taste activity–dependent pruning by microglia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512853/ https://www.ncbi.nlm.nih.gov/pubmed/37733279 http://dx.doi.org/10.1084/jem.20212476 |
work_keys_str_mv | AT sunchengsan maternaldietduringearlygestationinfluencespostnataltasteactivitydependentpruningbymicroglia AT zhengshuqiu maternaldietduringearlygestationinfluencespostnataltasteactivitydependentpruningbymicroglia AT perryjustinsa maternaldietduringearlygestationinfluencespostnataltasteactivitydependentpruningbymicroglia AT norrisgeoffreyt maternaldietduringearlygestationinfluencespostnataltasteactivitydependentpruningbymicroglia AT chengmei maternaldietduringearlygestationinfluencespostnataltasteactivitydependentpruningbymicroglia AT kongfanzhen maternaldietduringearlygestationinfluencespostnataltasteactivitydependentpruningbymicroglia AT skybergrolf maternaldietduringearlygestationinfluencespostnataltasteactivitydependentpruningbymicroglia AT cangjianhua maternaldietduringearlygestationinfluencespostnataltasteactivitydependentpruningbymicroglia AT erisiralev maternaldietduringearlygestationinfluencespostnataltasteactivitydependentpruningbymicroglia AT kipnisjonathan maternaldietduringearlygestationinfluencespostnataltasteactivitydependentpruningbymicroglia AT hilldavidl maternaldietduringearlygestationinfluencespostnataltasteactivitydependentpruningbymicroglia |