Ackerman Kate G, Greer John J
Division of Genetics, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Am J Med Genet C Semin Med Genet. 2007 May 15;145C(2):109-16. doi: 10.1002/ajmg.c.30128.
Improving our understanding of diaphragmatic development is essential to making progress in defining the pathogenesis and genetic etiologies of congenital diaphragmatic defects in humans. As mouse genetic technology has given us new tools to manipulate and observe development, a number of mouse models have recently emerged that provide valuable insight to this field. In this article, we review our current understanding of diaphragmatic embryogenesis including the origin of diaphragmatic tissue. We use rodent models to review the muscularization of the diaphragm and review selected genetic models of abnormal muscularization. We also review models of posterior diaphragmatic defects and discuss evidence for the pleuroperitoneal fold (PPF) tissue contributing to the diaphragm. Finally, we discuss models of anterior and central hernias. It may be simplistic to subdivide this review based on anatomic regions of the diaphragm, as evidence is emerging that defects in different regions of the diaphragm in humans and in mice may be etiologically related. However, at this time we do not have enough knowledge to make more mechanistic or genetic classifications though with time, genetic progress in the field of diaphragm development will allow us to do this.
增进我们对膈肌发育的理解对于在界定人类先天性膈缺陷的发病机制和遗传病因方面取得进展至关重要。由于小鼠基因技术为我们提供了操纵和观察发育的新工具,最近出现了一些小鼠模型,它们为该领域提供了有价值的见解。在本文中,我们回顾了目前对膈肌胚胎发生的理解,包括膈肌组织的起源。我们使用啮齿动物模型来回顾膈肌的肌化过程,并回顾选定的肌化异常的遗传模型。我们还回顾了后膈缺陷的模型,并讨论了胸膜腹膜皱襞(PPF)组织对膈肌形成有贡献的证据。最后,我们讨论前疝和中央疝的模型。基于膈肌的解剖区域来细分本综述可能过于简单,因为越来越多的证据表明,人类和小鼠膈肌不同区域的缺陷可能在病因上有关联。然而,目前我们没有足够的知识进行更具机制性或遗传性的分类,不过随着时间的推移,膈肌发育领域的基因研究进展将使我们能够做到这一点。