Wang Weicai, Jian Yutao, Cai Bin, Wang Miao, Chen Mu, Huang Hongzhang
Cleft Palate Craniofac J. 2017 Jul;54(4):391-399. doi: 10.1597/15-271. Epub 2016 Aug 3.
To characterize the prenatal and postnatal craniofacial bone development in mouse model of all-trans retinoic acid (ATRA) exposure at different ages by a quantitative and morphological analysis of skull morphology.
Pregnant mice were exposed to ATRA at embryonic day 10 (E10) and 13 (E13) by oral gavage. Skulls of mice embryos at E19.5 and adult mice at postnatal day 35 (P35) were collected for high-resolution microcomputed tomography (microCT) imaging scanning and section HE staining. Reconstruction and measurement of mouse skulls were performed for prenatal and postnatal analysis of the control and ATRA-exposed mice.
Craniofacial malformations in mouse models caused by ATRA exposure were age dependent. ATRA exposure at E10 induced cleft palate in 81.8% of the fetuses, whereas the palatine bone of E13-exposed mice was intact. Inhibitions of maxilla and mandible development with craniofacial asymmetry induced were observed at E19.5 and P35. Compared with control and E13-exposed mice, the palatine bones of E10-exposed mice were not elevated and were smaller in dimension. Some E10-exposed mice exhibited other craniofacial abnormalities, including premature fusion of mandibular symphysis with a missing mandibular incisor and a smaller mandible. Severe deviated snouts and amorphous craniofacial suture were detected in E13-exposed mice at P35.
These morphological variations in E10- and E13-exposed mice suggested that ATRA was teratogenic in craniofacial bone development in mice and the effect was age dependent.
通过对头骨形态进行定量和形态学分析,描述全反式维甲酸(ATRA)在不同年龄暴露的小鼠模型中产前和产后颅面骨的发育情况。
通过灌胃法在胚胎第10天(E10)和第13天(E13)给怀孕小鼠暴露于ATRA。收集E19.5的小鼠胚胎头骨和出生后第35天(P35)的成年小鼠头骨,进行高分辨率微型计算机断层扫描(microCT)成像扫描和切片HE染色。对对照组和ATRA暴露组小鼠的头骨进行重建和测量,用于产前和产后分析。
ATRA暴露引起的小鼠模型颅面畸形具有年龄依赖性。E10暴露于ATRA导致81.8%的胎儿出现腭裂,而E13暴露组小鼠的腭骨完好无损。在E19.5和P35观察到上颌骨和下颌骨发育受抑制,并伴有颅面不对称。与对照组和E13暴露组小鼠相比,E10暴露组小鼠的腭骨未升高且尺寸较小。一些E10暴露组小鼠表现出其他颅面异常,包括下颌联合过早融合、下颌切牙缺失和下颌骨较小。在P35时,E13暴露组小鼠检测到严重的口鼻部偏斜和颅面缝线不规则。
E10和E13暴露组小鼠的这些形态学变化表明,ATRA对小鼠颅面骨发育具有致畸性,且其作用具有年龄依赖性。