Cargando…
Serotonin-1A receptor, a psychiatric disease risk factor, influences offspring immunity via sex-dependent genetic nurture
Serotonin-1A receptor (5HT1AR) is highly expressed in corticolimbic regions and its deficit is associated with anxiety and depression. A similar reduction in 5HT1AR heterozygous knockout (Het) mice results in anxiety-like and increased stress-reactivity phenotypes. Here we describe immunological abn...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706704/ https://www.ncbi.nlm.nih.gov/pubmed/36458257 http://dx.doi.org/10.1016/j.isci.2022.105595 |
_version_ | 1784840563214778368 |
---|---|
author | Chen, Rosa J. Nabila, Anika Phalke, Swati Castro, Danny Flores Toth, Judit Gal Bergin, Paul Bastiaans, Jeroen Stuhlmann, Heidi Pernis, Alessandra B. Toth, Miklos |
author_facet | Chen, Rosa J. Nabila, Anika Phalke, Swati Castro, Danny Flores Toth, Judit Gal Bergin, Paul Bastiaans, Jeroen Stuhlmann, Heidi Pernis, Alessandra B. Toth, Miklos |
author_sort | Chen, Rosa J. |
collection | PubMed |
description | Serotonin-1A receptor (5HT1AR) is highly expressed in corticolimbic regions and its deficit is associated with anxiety and depression. A similar reduction in 5HT1AR heterozygous knockout (Het) mice results in anxiety-like and increased stress-reactivity phenotypes. Here we describe immunological abnormalities in Het females, characterized by an activated state of innate and adaptive immune cells. Het males showed only limited immune dysregulation. Similar immune abnormalities were present in the genetically WT female (F1) but not male offspring of Het mothers, indicating sex-specific immune system abnormalities that are dependent on the mother’s 5HT1AR deficit, known as maternal genetic effect or “genetic nurture”. Expression profiling of the maternal-fetal interface revealed reduced immune cell invasion to decidua and accelerated trophoblast migration. These data suggest that 5HT1AR deficit, by altering the maternal immune system and midgestational in utero environment, leads to sex-biased outcomes, predominantly immune dysregulation in the female and anxiety-like behavior in the male offspring. |
format | Online Article Text |
id | pubmed-9706704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-97067042022-11-30 Serotonin-1A receptor, a psychiatric disease risk factor, influences offspring immunity via sex-dependent genetic nurture Chen, Rosa J. Nabila, Anika Phalke, Swati Castro, Danny Flores Toth, Judit Gal Bergin, Paul Bastiaans, Jeroen Stuhlmann, Heidi Pernis, Alessandra B. Toth, Miklos iScience Article Serotonin-1A receptor (5HT1AR) is highly expressed in corticolimbic regions and its deficit is associated with anxiety and depression. A similar reduction in 5HT1AR heterozygous knockout (Het) mice results in anxiety-like and increased stress-reactivity phenotypes. Here we describe immunological abnormalities in Het females, characterized by an activated state of innate and adaptive immune cells. Het males showed only limited immune dysregulation. Similar immune abnormalities were present in the genetically WT female (F1) but not male offspring of Het mothers, indicating sex-specific immune system abnormalities that are dependent on the mother’s 5HT1AR deficit, known as maternal genetic effect or “genetic nurture”. Expression profiling of the maternal-fetal interface revealed reduced immune cell invasion to decidua and accelerated trophoblast migration. These data suggest that 5HT1AR deficit, by altering the maternal immune system and midgestational in utero environment, leads to sex-biased outcomes, predominantly immune dysregulation in the female and anxiety-like behavior in the male offspring. Elsevier 2022-11-15 /pmc/articles/PMC9706704/ /pubmed/36458257 http://dx.doi.org/10.1016/j.isci.2022.105595 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Chen, Rosa J. Nabila, Anika Phalke, Swati Castro, Danny Flores Toth, Judit Gal Bergin, Paul Bastiaans, Jeroen Stuhlmann, Heidi Pernis, Alessandra B. Toth, Miklos Serotonin-1A receptor, a psychiatric disease risk factor, influences offspring immunity via sex-dependent genetic nurture |
title | Serotonin-1A receptor, a psychiatric disease risk factor, influences offspring immunity via sex-dependent genetic nurture |
title_full | Serotonin-1A receptor, a psychiatric disease risk factor, influences offspring immunity via sex-dependent genetic nurture |
title_fullStr | Serotonin-1A receptor, a psychiatric disease risk factor, influences offspring immunity via sex-dependent genetic nurture |
title_full_unstemmed | Serotonin-1A receptor, a psychiatric disease risk factor, influences offspring immunity via sex-dependent genetic nurture |
title_short | Serotonin-1A receptor, a psychiatric disease risk factor, influences offspring immunity via sex-dependent genetic nurture |
title_sort | serotonin-1a receptor, a psychiatric disease risk factor, influences offspring immunity via sex-dependent genetic nurture |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706704/ https://www.ncbi.nlm.nih.gov/pubmed/36458257 http://dx.doi.org/10.1016/j.isci.2022.105595 |
work_keys_str_mv | AT chenrosaj serotonin1areceptorapsychiatricdiseaseriskfactorinfluencesoffspringimmunityviasexdependentgeneticnurture AT nabilaanika serotonin1areceptorapsychiatricdiseaseriskfactorinfluencesoffspringimmunityviasexdependentgeneticnurture AT phalkeswati serotonin1areceptorapsychiatricdiseaseriskfactorinfluencesoffspringimmunityviasexdependentgeneticnurture AT castrodannyflores serotonin1areceptorapsychiatricdiseaseriskfactorinfluencesoffspringimmunityviasexdependentgeneticnurture AT tothjuditgal serotonin1areceptorapsychiatricdiseaseriskfactorinfluencesoffspringimmunityviasexdependentgeneticnurture AT berginpaul serotonin1areceptorapsychiatricdiseaseriskfactorinfluencesoffspringimmunityviasexdependentgeneticnurture AT bastiaansjeroen serotonin1areceptorapsychiatricdiseaseriskfactorinfluencesoffspringimmunityviasexdependentgeneticnurture AT stuhlmannheidi serotonin1areceptorapsychiatricdiseaseriskfactorinfluencesoffspringimmunityviasexdependentgeneticnurture AT pernisalessandrab serotonin1areceptorapsychiatricdiseaseriskfactorinfluencesoffspringimmunityviasexdependentgeneticnurture AT tothmiklos serotonin1areceptorapsychiatricdiseaseriskfactorinfluencesoffspringimmunityviasexdependentgeneticnurture |