Savolainen Saija M, Foley Julie F, Elmore Susan A
NIEHS, Cellular and Molecular Pathology Branch, Research Triangle Park, North Carolina 27709, USA.
Toxicol Pathol. 2009 Jun;37(4):395-414. doi: 10.1177/0192623309335060. Epub 2009 Apr 9.
In humans, congenital heart diseases are common. Since the rapid progression of transgenic technologies, the mouse has become the major animal model of defective cardiovascular development. Moreover, genetically modified mice frequently die in utero, commonly due to abnormal cardiovascular development. A variety of publications address specific developmental stages or structures of the mouse heart, but a single reference reviewing and describing the anatomy and histology of cardiac developmental events, stage by stage, has not been available. The aim of this color atlas, which demonstrates embryonic/fetal heart development, is to provide a tool for pathologists and biomedical scientists to use for detailed histological evaluation of hematoxylin and eosin (H&E)-stained sections of the developing mouse heart with emphasis on embryonic days (E) 11.5-18.5. The selected images illustrate the main structures and developmental events at each stage and serve as reference material for the confirmation of the chronological age of the embryo/early fetus and assist in the identification of any abnormalities. An extensive review of the literature covering cardiac development pre-E11.5 is summarized in the introduction. Although the focus of this atlas is on the descriptive anatomic and histological development of the normal mouse heart from E11.5 to E18.5, potential embryonic cardiac lesions are discussed with a list of the most common transgenic pre- and perinatal heart defects. Representative images of hearts at E11.5-15.5 and E18.5 are provided in Figures 2-4, 6, 8, and 9. A complete set of labeled images (Figures E11.5-18.5) is available on the CD enclosed in this issue of Toxicologic Pathology. All digital images can be viewed online at https://niehsimages.epl-inc.com with the username "ToxPath" and the password "embryohearts."
在人类中,先天性心脏病很常见。自从转基因技术迅速发展以来,小鼠已成为心血管发育缺陷的主要动物模型。此外,基因改造小鼠常在子宫内死亡,通常是由于心血管发育异常。许多出版物都涉及小鼠心脏的特定发育阶段或结构,但尚未有一份单一参考文献能逐阶段回顾和描述心脏发育事件的解剖学和组织学。本彩色图谱旨在展示胚胎/胎儿心脏发育,为病理学家和生物医学科学家提供一种工具,以便他们对发育中小鼠心脏苏木精和伊红(H&E)染色切片进行详细的组织学评估,重点是胚胎第11.5 - 18.5天。所选图像展示了每个阶段的主要结构和发育事件,可作为参考资料用于确认胚胎/早期胎儿的实际年龄,并有助于识别任何异常情况。引言部分总结了对涵盖胚胎第11.5天之前心脏发育的文献的广泛综述。尽管本图谱的重点是正常小鼠心脏从胚胎第11.5天到第18.5天的描述性解剖学和组织学发育,但也讨论了潜在的胚胎心脏病变,并列出了最常见的转基因产前和围产期心脏缺陷。图2 - 4、6、8和9提供了胚胎第11.5 - 15.5天和第18.5天心脏的代表性图像。本期《毒理病理学》随附的光盘上有一套完整的标注图像(图E11.5 - 至18.5)。所有数字图像均可通过https://niehsimages.epl-inc.com在线查看,用户名是“ToxPath”,密码是“embryohearts”。