Martínez-Cerdeño Verónica, Camacho Jasmin, Fox Elizabeth, Miller Elaine, Ariza Jeanelle, Kienzle Devon, Plank Kaela, Noctor Stephen C, Van de Water Judy
Department of Pathology and Laboratory Medicine.
MIND Institute.
Cereb Cortex. 2016 Jan;26(1):374-383. doi: 10.1093/cercor/bhu291. Epub 2014 Dec 22.
Autism spectrum disorders (ASDs) affect up to 1 in 68 children. Autism-specific autoantibodies directed against fetal brain proteins have been found exclusively in a subpopulation of mothers whose children were diagnosed with ASD or maternal autoantibody-related autism. We tested the impact of autoantibodies on brain development in mice by transferring human antigen-specific IgG directly into the cerebral ventricles of embryonic mice during cortical neurogenesis. We show that autoantibodies recognize radial glial cells during development. We also show that prenatal exposure to autism-specific maternal autoantibodies increased stem cell proliferation in the subventricular zone (SVZ) of the embryonic neocortex, increased adult brain size and weight, and increased the size of adult cortical neurons. We propose that prenatal exposure to autism-specific maternal autoantibodies directly affects radial glial cell development and presents a viable pathologic mechanism for the maternal autoantibody-related prenatal ASD risk factor.
自闭症谱系障碍(ASD)影响着每68名儿童中的1名。针对胎儿脑蛋白的自闭症特异性自身抗体仅在其子女被诊断为ASD或患有母体自身抗体相关自闭症的母亲亚群中被发现。我们通过在皮质神经发生期间将人类抗原特异性IgG直接注入胚胎小鼠的脑室,测试了自身抗体对小鼠大脑发育的影响。我们发现自身抗体在发育过程中识别放射状胶质细胞。我们还表明,产前暴露于自闭症特异性母体自身抗体可增加胚胎新皮质脑室下区(SVZ)的干细胞增殖,增加成年大脑的大小和重量,并增加成年皮质神经元的大小。我们提出,产前暴露于自闭症特异性母体自身抗体直接影响放射状胶质细胞的发育,并为母体自身抗体相关的产前ASD危险因素提供了一种可行的病理机制。