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      Decreased reelin expression and organophosphate pesticide exposure alters mouse behaviour and brain morphology

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          Abstract

          Genetic and environmental factors are both likely to contribute to neurodevelopmental disorders, including ASDs (autism spectrum disorders). In this study, we examined the combinatorial effect of two factors thought to be involved in autism – reduction in the expression of the extracellular matrix protein reelin and prenatal exposure to an organophosphate pesticide, CPO (chlorpyrifos oxon). Mice with reduced reelin expression or prenatal exposure to CPO exhibited subtle changes in ultrasound vocalization, open field behaviour, social interaction and repetitive behaviour. Paradoxically, mice exposed to both variables often exhibited a mitigation of abnormal behaviours, rather than increased behavioural abnormalities as expected. We identified specific differences in males and females in response to both of these variables. In addition to behavioural abnormalities, we identified anatomical alterations in the olfactory bulb, piriform cortex, hippocampus and cerebellum. As with our behavioural studies, anatomical alterations appeared to be ameliorated in the presence of both variables. While these observations support an interaction between loss of reelin expression and CPO exposure, our results suggest a complexity to this interaction beyond an additive effect of individual phenotypes.

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          Most cited references59

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          Advances in autism genetics: on the threshold of a new neurobiology.

          Autism is a heterogeneous syndrome defined by impairments in three core domains: social interaction, language and range of interests. Recent work has led to the identification of several autism susceptibility genes and an increased appreciation of the contribution of de novo and inherited copy number variation. Promising strategies are also being applied to identify common genetic risk variants. Systems biology approaches, including array-based expression profiling, are poised to provide additional insights into this group of disorders, in which heterogeneity, both genetic and phenotypic, is emerging as a dominant theme.
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            A protein related to extracellular matrix proteins deleted in the mouse mutant reeler.

            The autosomal recessive mouse mutation reeler leads to impaired motor coordination, tremors and ataxia. Neurons in affected mice fail to reach their correct locations in the developing brain, disrupting the organization of the cerebellar and cerebral cortices and other laminated regions. Here we use a previously characterized reeler allele (rl(tg)) to close a gene, reelin, deleted in two reeler alleles. Normal but not mutant mice express reelin in embryonic and postnatal neurons during periods of neuronal migration. The encoded protein resembles extracellular matrix proteins involved in cell adhesion. The reeler phenotype thus seems to reflect a failure of early events associated with brain lamination which are normally controlled by reelin.
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              The epidemiology of autism spectrum disorders.

              Autism spectrum disorders (ASDs) are complex, lifelong, neurodevelopmental conditions of largely unknown cause. They are much more common than previously believed, second in frequency only to mental retardation among the serious developmental disorders. Although a heritable component has been demonstrated in ASD etiology, putative risk genes have yet to be identified. Environmental risk factors may also play a role, perhaps via complex gene-environment interactions, but no specific exposures with significant population effects are known. A number of endogenous biomarkers associated with autism risk have been investigated, and these may help identify significant biologic pathways that, in turn, will aid in the discovery of specific genes and exposures. Future epidemiologic research should focus on expanding population-based descriptive data on ASDs, exploring candidate risk factors in large well-designed studies incorporating both genetic and environmental exposure data and addressing possible etiologic heterogeneity in studies that can stratify case groups and consider alternate endophenotypes.
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                Author and article information

                Journal
                ASN Neuro
                ASN Neuro
                ASN
                ASN NEURO
                American Society for Neurochemistry (9037 Ron Den Lane, Windermere, FL 34786, U.S.A. )
                1759-0914
                8 January 2013
                18 February 2012
                2013
                : 5
                : 1
                : e00106
                Affiliations
                Department of Psychiatry and Biobehavioral Science, UCLA School of Medicine, Los Angeles, CA 90095, U.S.A.
                Author notes
                1To whom correspondence should be addressed (email Ecarpenter@ 123456mednet.ucla.edu ).
                Article
                AN20120060
                10.1042/AN20120060
                3575035
                23298182
                32fafbc2-4aa3-48d9-8bb6-cad1339dd248
                © 2013 The Author(s).

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Licence ( http://creativecommons.org/licenses/by-nc/2.5/) which permits unrestricted non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 12 September 2012
                : 2 January 2013
                : 8 January 2012
                Page count
                Figures: 11, Tables: 1, References: 56, Pages: 16
                Categories
                Research Article
                S2
                S12

                Neurosciences
                autism,cerebellum,hippocampus,olfactory bulb,reeler,social interaction,ultrasonic communication,ache, acetylcholinesterase,adhd, attention deficit hyperactivity disorder,asd, autism spectrum disorder,cpo, chlorpyrifos oxon,ecl, enhanced chemiluminescence,wt, wild-type

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