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Effects of Maternal Immune Activation on Gene Expression Patterns in the Fetal Brain

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Date 2012 Jul 27
PMID 22832908
Citations 85
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Abstract

We are exploring the mechanisms underlying how maternal infection increases the risk for schizophrenia and autism in the offspring. Several mouse models of maternal immune activation (MIA) were used to examine the immediate effects of MIA induced by influenza virus, poly(I:C) and interleukin IL-6 on the fetal brain transcriptome. Our results indicate that all three MIA treatments lead to strong and common gene expression changes in the embryonic brain. Most notably, there is an acute and transient upregulation of the α, β and γ crystallin gene family. Furthermore, levels of crystallin gene expression are correlated with the severity of MIA as assessed by placental weight. The overall gene expression changes suggest that the response to MIA is a neuroprotective attempt by the developing brain to counteract environmental stress, but at a cost of disrupting typical neuronal differentiation and axonal growth. We propose that this cascade of events might parallel the mechanisms by which environmental insults contribute to the risk of neurodevelopmental disorders such as schizophrenia and autism.

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References
1.
Meyer U, Nyffeler M, Schwendener S, Knuesel I, Yee B, Feldon J . Relative prenatal and postnatal maternal contributions to schizophrenia-related neurochemical dysfunction after in utero immune challenge. Neuropsychopharmacology. 2007; 33(2):441-56. DOI: 10.1038/sj.npp.1301413. View

2.
Liedtke T, Schwamborn J, Schroer U, Thanos S . Elongation of axons during regeneration involves retinal crystallin beta b2 (crybb2). Mol Cell Proteomics. 2007; 6(5):895-907. DOI: 10.1074/mcp.M600245-MCP200. View

3.
Stoevring B, Vang O, Christiansen M . (alpha)B-crystallin in cerebrospinal fluid of patients with multiple sclerosis. Clin Chim Acta. 2005; 356(1-2):95-101. DOI: 10.1016/j.cccn.2005.01.034. View

4.
Wu N, Wang Y, Zhao H, Liu D, Ying X, Yin Z . alpha-Crystallin downregulates the expression of TNF-alpha and iNOS by activated rat retinal microglia in vitro and in vivo. Ophthalmic Res. 2009; 42(1):21-8. DOI: 10.1159/000219681. View

5.
Bajramovic J, Lassmann H, van Noort J . Expression of alphaB-crystallin in glia cells during lesional development in multiple sclerosis. J Neuroimmunol. 1997; 78(1-2):143-51. DOI: 10.1016/s0165-5728(97)00092-1. View