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肥胖小鼠的椎体和肋骨形态紊乱。与人类脊柱侧弯的结构关系。

Disordered vertebral and rib morphology in pudgy mice. Structural relationships to human scoliosis.

作者信息

Shapiro Frederic

机构信息

Laboratory for the Study of Skeletal Disorders, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Adv Anat Embryol Cell Biol. 2016;221:1-123. doi: 10.1007/978-3-319-43151-2_1.

Abstract

Normal and abnormal vertebral development have been studied over the past 200 years at increasing levels of resolution as techniques for biological investigation have improved. Disordered development of the axial skeleton from the early embryonic period on leads to structurally malformed vertebrae and intervertebral discs and ribs causing the severe deformities of scoliosis, kyphosis, and kyphoscoliosis. Developmental malformation of the axial skeleton therefore has led to considerable biological and clinical interest. This work will detail our studies on the structural deformities of the vertebral column and adjacent ribs in the pudgy mouse [1] caused by mutations in the delta-like 3 (Dll3) gene of the Notch family [2]. While gene abnormalities in the pudgy mouse have been outlined, there has been no in-depth assessment of the histopathology of the pudgy vertebral and rib abnormalities that this study will provide. In addition, although congenital scoliosis has been recognized as a clinical problem since the mid-nineteenth century (1800s) [3] and accurately defined by radiography since the early twentieth century (1900s) [4-6], there have been few detailed histopathologic studies of human cases. We will also relate our histopathologic findings in the pudgy mouse to the histopathology of human vertebral and rib malformations in clinical cases of congenital scoliosis, one of which we defined in detail previously [7].

摘要

在过去的200年里,随着生物学研究技术的不断进步,人们对正常和异常的脊椎发育进行了越来越高分辨率的研究。从胚胎早期开始,轴向骨骼的发育紊乱会导致椎骨、椎间盘和肋骨结构畸形,从而引起脊柱侧凸、脊柱后凸和脊柱侧后凸等严重畸形。因此,轴向骨骼的发育畸形引起了相当大的生物学和临床关注。这项工作将详细介绍我们对矮胖小鼠[1]中由Notch家族的delta样3(Dll3)基因突变引起的脊柱和相邻肋骨结构畸形的研究[2]。虽然已经概述了矮胖小鼠中的基因异常,但本研究将对矮胖小鼠脊柱和肋骨异常的组织病理学进行深入评估。此外,尽管先天性脊柱侧凸自19世纪中叶(1800年代)[3]就被确认为临床问题,自20世纪初(1900年代)[4 - 6]通过放射学准确界定,但对人类病例的详细组织病理学研究却很少。我们还将把在矮胖小鼠中的组织病理学发现与先天性脊柱侧凸临床病例中人类脊柱和肋骨畸形的组织病理学联系起来,我们之前曾详细定义过其中一个病例[7]。

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