Ron Schaer , Nicole Wenger , Felisa Herrero , Tina Notter , Urs Meyer
{"title":"母体免疫激活小鼠模型中恢复力和易感性的个体发生和可塑性。","authors":"Ron Schaer , Nicole Wenger , Felisa Herrero , Tina Notter , Urs Meyer","doi":"10.1016/j.bbi.2025.06.040","DOIUrl":null,"url":null,"abstract":"<div><div>Maternal immune activation (MIA) during pregnancy results in variable neurodevelopmental and behavioral outcomes in both humans and animal models. In a mouse model of MIA using prenatal poly(I:C) administration, we recently identified subgroups of MIA-exposed offspring with distinct behavioral and transcriptional profiles even under genetic homogeneity. Here, we used the same model to explore whether the expression of resilient and susceptible phenotypes after MIA represents stable traits or whether they exhibit plasticity throughout adolescent maturation. Conducting longitudinal testing in a first cohort, we revealed that MIA offspring can be stratified into subgroups with distinct behavioral profiles at juvenile age. This early divergence was sex-dependent and predictive of different behavioral outcomes at adult age. In a second cohort, we examined the effects of repeated social intervention during peri-adolescence on brain and behavioral trajectories. In male MIA offspring displaying juvenile deficits in sociability and hyperactivity, the intervention did not alleviate adult deficits in sociability or temporal order memory but prevented the adult emergence of prepulse inhibition impairments. Conversely, in female MIA offspring with juvenile social deficits, the intervention improved adult deficits in sociability and temporal order memory, but it failed to normalize adult impairments in prepulse inhibition. These sex-specific behavioral outcomes were paralleled by subgroup-specific changes in oxytocinergic and dopaminergic markers in cortical and subcortical brain regions. Together, our findings indicate that MIA-exposed offspring can be stratified into distinct subgroups early in life, with subsequent risk and resilience trajectories varying by sex. Moreover, our data identify a window of plasticity during which targeted interventions can modulate abnormal maturational trajectories, ultimately mitigating the long-term effects of MIA in a sex-dependent manner.</div></div>","PeriodicalId":9199,"journal":{"name":"Brain, Behavior, and Immunity","volume":"129 ","pages":"Pages 666-680"},"PeriodicalIF":7.6000,"publicationDate":"2025-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ontogeny and plasticity of resilience and susceptibility in a mouse model of maternal immune activation\",\"authors\":\"Ron Schaer , Nicole Wenger , Felisa Herrero , Tina Notter , Urs Meyer\",\"doi\":\"10.1016/j.bbi.2025.06.040\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Maternal immune activation (MIA) during pregnancy results in variable neurodevelopmental and behavioral outcomes in both humans and animal models. In a mouse model of MIA using prenatal poly(I:C) administration, we recently identified subgroups of MIA-exposed offspring with distinct behavioral and transcriptional profiles even under genetic homogeneity. Here, we used the same model to explore whether the expression of resilient and susceptible phenotypes after MIA represents stable traits or whether they exhibit plasticity throughout adolescent maturation. Conducting longitudinal testing in a first cohort, we revealed that MIA offspring can be stratified into subgroups with distinct behavioral profiles at juvenile age. This early divergence was sex-dependent and predictive of different behavioral outcomes at adult age. In a second cohort, we examined the effects of repeated social intervention during peri-adolescence on brain and behavioral trajectories. In male MIA offspring displaying juvenile deficits in sociability and hyperactivity, the intervention did not alleviate adult deficits in sociability or temporal order memory but prevented the adult emergence of prepulse inhibition impairments. Conversely, in female MIA offspring with juvenile social deficits, the intervention improved adult deficits in sociability and temporal order memory, but it failed to normalize adult impairments in prepulse inhibition. These sex-specific behavioral outcomes were paralleled by subgroup-specific changes in oxytocinergic and dopaminergic markers in cortical and subcortical brain regions. Together, our findings indicate that MIA-exposed offspring can be stratified into distinct subgroups early in life, with subsequent risk and resilience trajectories varying by sex. Moreover, our data identify a window of plasticity during which targeted interventions can modulate abnormal maturational trajectories, ultimately mitigating the long-term effects of MIA in a sex-dependent manner.</div></div>\",\"PeriodicalId\":9199,\"journal\":{\"name\":\"Brain, Behavior, and Immunity\",\"volume\":\"129 \",\"pages\":\"Pages 666-680\"},\"PeriodicalIF\":7.6000,\"publicationDate\":\"2025-07-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Brain, Behavior, and Immunity\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0889159125002570\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain, Behavior, and Immunity","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0889159125002570","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
Ontogeny and plasticity of resilience and susceptibility in a mouse model of maternal immune activation
Maternal immune activation (MIA) during pregnancy results in variable neurodevelopmental and behavioral outcomes in both humans and animal models. In a mouse model of MIA using prenatal poly(I:C) administration, we recently identified subgroups of MIA-exposed offspring with distinct behavioral and transcriptional profiles even under genetic homogeneity. Here, we used the same model to explore whether the expression of resilient and susceptible phenotypes after MIA represents stable traits or whether they exhibit plasticity throughout adolescent maturation. Conducting longitudinal testing in a first cohort, we revealed that MIA offspring can be stratified into subgroups with distinct behavioral profiles at juvenile age. This early divergence was sex-dependent and predictive of different behavioral outcomes at adult age. In a second cohort, we examined the effects of repeated social intervention during peri-adolescence on brain and behavioral trajectories. In male MIA offspring displaying juvenile deficits in sociability and hyperactivity, the intervention did not alleviate adult deficits in sociability or temporal order memory but prevented the adult emergence of prepulse inhibition impairments. Conversely, in female MIA offspring with juvenile social deficits, the intervention improved adult deficits in sociability and temporal order memory, but it failed to normalize adult impairments in prepulse inhibition. These sex-specific behavioral outcomes were paralleled by subgroup-specific changes in oxytocinergic and dopaminergic markers in cortical and subcortical brain regions. Together, our findings indicate that MIA-exposed offspring can be stratified into distinct subgroups early in life, with subsequent risk and resilience trajectories varying by sex. Moreover, our data identify a window of plasticity during which targeted interventions can modulate abnormal maturational trajectories, ultimately mitigating the long-term effects of MIA in a sex-dependent manner.
期刊介绍:
Established in 1987, Brain, Behavior, and Immunity proudly serves as the official journal of the Psychoneuroimmunology Research Society (PNIRS). This pioneering journal is dedicated to publishing peer-reviewed basic, experimental, and clinical studies that explore the intricate interactions among behavioral, neural, endocrine, and immune systems in both humans and animals.
As an international and interdisciplinary platform, Brain, Behavior, and Immunity focuses on original research spanning neuroscience, immunology, integrative physiology, behavioral biology, psychiatry, psychology, and clinical medicine. The journal is inclusive of research conducted at various levels, including molecular, cellular, social, and whole organism perspectives. With a commitment to efficiency, the journal facilitates online submission and review, ensuring timely publication of experimental results. Manuscripts typically undergo peer review and are returned to authors within 30 days of submission. It's worth noting that Brain, Behavior, and Immunity, published eight times a year, does not impose submission fees or page charges, fostering an open and accessible platform for scientific discourse.