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视黄酸缺乏与胎儿酒精谱系障碍中颅面畸形和小头畸形的诱导机制研究

Insights into retinoic acid deficiency and the induction of craniofacial malformations and microcephaly in fetal alcohol spectrum disorder.

作者信息

Petrelli Berardino, Bendelac Liat, Hicks Geoffrey G, Fainsod Abraham

机构信息

Regenerative Medicine Program and the Department of Biochemistry & Medical Genetics, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.

Department of Developmental Biology and Cancer Research, Institute for Medical Research Israel-Canada, Faculty of Medicine, Hebrew University, Jerusalem, Israel.

出版信息

Genesis. 2019 Jan;57(1):e23278. doi: 10.1002/dvg.23278. Epub 2019 Jan 21.

Abstract

Fetal Alcohol Spectrum Disorder (FASD) is a set of neurodevelopmental malformations caused by maternal consumption of alcohol during pregnancy. FASD sentinel facial features are unique to the disorder, and microcephaly is common in severe forms of FASD. Retinoic acid deficiency has been shown to cause craniofacial malformations and microcephaly in animal models reminiscent of those caused by prenatal alcohol exposure. Alcohol exposure affects the migration and survival of cranial neural crest cells, which are required for proper frontonasal prominence and pharyngeal arch development. Defects in craniofacial development are further amplified by the many downstream pathways that are transcriptionally controlled retinoic acid target genes, including Shh signaling. Recent evidence shows that alcohol exposure itself is sufficient to induce retinoic acid deficiency in the embryo. These data suggest that retinoic acid deficiency is an important underlying etiology of FASD. In disorders like Vitamin A Deficiency, FASD, DiGeorge (22q11.2 Deletion Syndrome), CHARGE, Smith-Magenis, Matthew-Wood, and Congenital Zika Syndromes, evidence is accumulating to link reduced retinoic acid signaling with developmental defects like craniofacial malformations and microcephaly. Research focus on characterizing the effects of retinoic acid deficiency during early development and on understanding the downstream signaling pathways involved in aberrant head, and craniofacial development will reveal underlying etiologies of these disorders.

摘要

胎儿酒精谱系障碍(FASD)是一组由母亲在孕期饮酒导致的神经发育畸形。FASD标志性面部特征是该疾病所特有的,小头畸形在严重形式的FASD中很常见。在动物模型中,已证明视黄酸缺乏会导致颅面畸形和小头畸形,这与产前酒精暴露所引起的情况相似。酒精暴露会影响颅神经嵴细胞的迁移和存活,而这些细胞对于正常的额鼻突出和咽弓发育是必需的。颅面发育缺陷会因许多下游通路而进一步加剧,这些通路是受转录调控的视黄酸靶基因,包括Shh信号通路。最近的证据表明,酒精暴露本身就足以在胚胎中诱导视黄酸缺乏。这些数据表明,视黄酸缺乏是FASD的一个重要潜在病因。在维生素A缺乏症、FASD、22q11.2缺失综合征、CHARGE综合征、史密斯-马吉尼斯综合征、马修-伍德综合征和先天性寨卡综合征等疾病中,越来越多的证据表明视黄酸信号减少与颅面畸形和小头畸形等发育缺陷有关。对早期发育过程中视黄酸缺乏的影响进行特征描述以及对异常头部和颅面发育所涉及的下游信号通路的理解的研究,将揭示这些疾病的潜在病因。

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