Altered Postnatal Cell Proliferation in Brains of Mouse Pups Prenatally Exposed to IgG from Mothers of Children with Autistic Disorder

Auto antibodies found in the mothers of children with autistic disorder (MCAD) when passively transferred to pregnant mice cause behavioral alterations in juvenile and adult offspring. The goal of this study was to identify whether intraperitoneal injection of MCAD-IgG during gestation affected post...

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Main Authors: Shilpa D. Kadam, Beth M. French, S-T. Kim, Christy M. Morris-Berry, Andrew W. Zimmerman, Mary E. Blue, Harvey S. Singer
Format: Article
Language:English
Published: SAGE Publishing 2013-01-01
Series:Journal of Experimental Neuroscience
Online Access:https://doi.org/10.4137/JEN.S12979
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author Shilpa D. Kadam
Beth M. French
S-T. Kim
Christy M. Morris-Berry
Andrew W. Zimmerman
Mary E. Blue
Harvey S. Singer
author_facet Shilpa D. Kadam
Beth M. French
S-T. Kim
Christy M. Morris-Berry
Andrew W. Zimmerman
Mary E. Blue
Harvey S. Singer
author_sort Shilpa D. Kadam
collection DOAJ
description Auto antibodies found in the mothers of children with autistic disorder (MCAD) when passively transferred to pregnant mice cause behavioral alterations in juvenile and adult offspring. The goal of this study was to identify whether intraperitoneal injection of MCAD-IgG during gestation affected postnatal cell proliferation and survival in P7 offspring. Pooled MCAD-IgG or IgG from mothers of unaffected children (MUC) or phosphate-buffered saline was injected daily into C57BL/J6 pregnant dams (gestational days E13–E18). MCAD-IgG exposure significantly increased cell proliferation in the subventricular and subgranular zones. In contrast, BrdU-labeled cells on P1 and surviving until P7 (P1-generated cells) showed reduced cell densities in layers 2–4 of frontal and parietal cortices of MCAD mice compared to those in MUC and PBS-injected mice. In conclusion, significant increases in cell proliferation at P7 and reduced densities of P1-generated cells distinguish in utero exposure to MCAD compared to MUC and PBS.
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spelling doaj.art-2ca56fddd27348d5a70240b7394d1c732022-12-21T19:57:22ZengSAGE PublishingJournal of Experimental Neuroscience1179-06952013-01-01710.4137/JEN.S12979Altered Postnatal Cell Proliferation in Brains of Mouse Pups Prenatally Exposed to IgG from Mothers of Children with Autistic DisorderShilpa D. Kadam0Beth M. French1S-T. Kim2Christy M. Morris-Berry3Andrew W. Zimmerman4Mary E. Blue5Harvey S. Singer6Departments of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.Neuroscience Laboratory, Hugo W Moser Research Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.Department of Neurology and Developmental Medicine at Kennedy Krieger, Johns Hopkins University School of Medicine, Baltimore, MD, USA.Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, USA.Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.Auto antibodies found in the mothers of children with autistic disorder (MCAD) when passively transferred to pregnant mice cause behavioral alterations in juvenile and adult offspring. The goal of this study was to identify whether intraperitoneal injection of MCAD-IgG during gestation affected postnatal cell proliferation and survival in P7 offspring. Pooled MCAD-IgG or IgG from mothers of unaffected children (MUC) or phosphate-buffered saline was injected daily into C57BL/J6 pregnant dams (gestational days E13–E18). MCAD-IgG exposure significantly increased cell proliferation in the subventricular and subgranular zones. In contrast, BrdU-labeled cells on P1 and surviving until P7 (P1-generated cells) showed reduced cell densities in layers 2–4 of frontal and parietal cortices of MCAD mice compared to those in MUC and PBS-injected mice. In conclusion, significant increases in cell proliferation at P7 and reduced densities of P1-generated cells distinguish in utero exposure to MCAD compared to MUC and PBS.https://doi.org/10.4137/JEN.S12979
spellingShingle Shilpa D. Kadam
Beth M. French
S-T. Kim
Christy M. Morris-Berry
Andrew W. Zimmerman
Mary E. Blue
Harvey S. Singer
Altered Postnatal Cell Proliferation in Brains of Mouse Pups Prenatally Exposed to IgG from Mothers of Children with Autistic Disorder
Journal of Experimental Neuroscience
title Altered Postnatal Cell Proliferation in Brains of Mouse Pups Prenatally Exposed to IgG from Mothers of Children with Autistic Disorder
title_full Altered Postnatal Cell Proliferation in Brains of Mouse Pups Prenatally Exposed to IgG from Mothers of Children with Autistic Disorder
title_fullStr Altered Postnatal Cell Proliferation in Brains of Mouse Pups Prenatally Exposed to IgG from Mothers of Children with Autistic Disorder
title_full_unstemmed Altered Postnatal Cell Proliferation in Brains of Mouse Pups Prenatally Exposed to IgG from Mothers of Children with Autistic Disorder
title_short Altered Postnatal Cell Proliferation in Brains of Mouse Pups Prenatally Exposed to IgG from Mothers of Children with Autistic Disorder
title_sort altered postnatal cell proliferation in brains of mouse pups prenatally exposed to igg from mothers of children with autistic disorder
url https://doi.org/10.4137/JEN.S12979
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