Altered inflammatory response in FMRP-deficient microglia

Summary: Fragile X syndrome (FXS) is an inherited intellectual disability with a high risk for comorbid autism spectrum disorders. Since FXS is a genetic disease, patients are more susceptible to environmental factors aggravating symptomatology. However, this confounding interaction between FXS envi...

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Autores principales: Jennifer M. Parrott, Thomas Oster, Hye Young Lee
Formato: article
Lenguaje:EN
Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/e088359eab28482abe400d2c0c18a0df
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spelling oai:doaj.org-article:e088359eab28482abe400d2c0c18a0df2021-11-20T05:09:32ZAltered inflammatory response in FMRP-deficient microglia2589-004210.1016/j.isci.2021.103293https://doaj.org/article/e088359eab28482abe400d2c0c18a0df2021-11-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2589004221012621https://doaj.org/toc/2589-0042Summary: Fragile X syndrome (FXS) is an inherited intellectual disability with a high risk for comorbid autism spectrum disorders. Since FXS is a genetic disease, patients are more susceptible to environmental factors aggravating symptomatology. However, this confounding interaction between FXS environmental and genetic risk factors is under-investigated. Here, Fmr1 knock-out (KO) mice and the immune stimulus lipopolysaccharide (LPS) were used to explore this interaction between FXS development and inflammation in microglia, the brain’s primary immune cell. Our results demonstrate that Fmr1 KO and wild-type (WT) microglia are not different in inflammatory outcomes without LPS. However, Fmr1 KO microglia produces an elevated pro-inflammatory and phagocytic response following LPS treatment when compared to WT microglia. Our experiments also revealed baseline differences in mitochondrial function and morphology between WT and Fmr1 KO microglia, which LPS treatment exaggerated. Our data suggest an altered inflammatory mechanism in Fmr1 KO microglia implicating a gene and environment interaction.Jennifer M. ParrottThomas OsterHye Young LeeElsevierarticleMolecular biologyNeuroscienceImmunologyScienceQENiScience, Vol 24, Iss 11, Pp 103293- (2021)
institution DOAJ
collection DOAJ
language EN
topic Molecular biology
Neuroscience
Immunology
Science
Q
spellingShingle Molecular biology
Neuroscience
Immunology
Science
Q
Jennifer M. Parrott
Thomas Oster
Hye Young Lee
Altered inflammatory response in FMRP-deficient microglia
description Summary: Fragile X syndrome (FXS) is an inherited intellectual disability with a high risk for comorbid autism spectrum disorders. Since FXS is a genetic disease, patients are more susceptible to environmental factors aggravating symptomatology. However, this confounding interaction between FXS environmental and genetic risk factors is under-investigated. Here, Fmr1 knock-out (KO) mice and the immune stimulus lipopolysaccharide (LPS) were used to explore this interaction between FXS development and inflammation in microglia, the brain’s primary immune cell. Our results demonstrate that Fmr1 KO and wild-type (WT) microglia are not different in inflammatory outcomes without LPS. However, Fmr1 KO microglia produces an elevated pro-inflammatory and phagocytic response following LPS treatment when compared to WT microglia. Our experiments also revealed baseline differences in mitochondrial function and morphology between WT and Fmr1 KO microglia, which LPS treatment exaggerated. Our data suggest an altered inflammatory mechanism in Fmr1 KO microglia implicating a gene and environment interaction.
format article
author Jennifer M. Parrott
Thomas Oster
Hye Young Lee
author_facet Jennifer M. Parrott
Thomas Oster
Hye Young Lee
author_sort Jennifer M. Parrott
title Altered inflammatory response in FMRP-deficient microglia
title_short Altered inflammatory response in FMRP-deficient microglia
title_full Altered inflammatory response in FMRP-deficient microglia
title_fullStr Altered inflammatory response in FMRP-deficient microglia
title_full_unstemmed Altered inflammatory response in FMRP-deficient microglia
title_sort altered inflammatory response in fmrp-deficient microglia
publisher Elsevier
publishDate 2021
url https://doaj.org/article/e088359eab28482abe400d2c0c18a0df
work_keys_str_mv AT jennifermparrott alteredinflammatoryresponseinfmrpdeficientmicroglia
AT thomasoster alteredinflammatoryresponseinfmrpdeficientmicroglia
AT hyeyounglee alteredinflammatoryresponseinfmrpdeficientmicroglia
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