Genetics Unit, Shriners Hospital for Children, McGill University, Montreal, Quebec, Canada.
Spine (Phila Pa 1976). 2011 Jun 15;36(14):E914-20. doi: 10.1097/BRS.0b013e3181f1e84f.
Histologic analysis of spine development in cartilage-specific knockout mice.
To evaluate the role hyaluronan produced by hyaluronan synthase-2 (Has2) in spine development.
The Has2 gene is responsible for most hyaluronan production throughout the body, including the skeleton. However, it is not possible to study the involvement of hyaluronan in skeletal development using constitutive Has2 knockout mice, as the embryonic mice die early before skeletal development has occurred. This problem can be overcome by the use of cartilage-specific knockout mice.
Mice possessing floxed Has2 genes were crossed with mice expressing Cre recombinase under control of the type II collagen promoter to generate cartilage-specific Has2 knockout mice. Spine development was studied by histology.
Knockout mice died near birth and displayed severe abnormality in skeletal development. The spine showed defects in vertebral body size and the formation of the intervertebral discs. There was no evidence for the formation of an organized primary center of ossification within the vertebrae, and the appearance and organization of the hypertrophic chondrocytes was abnormal. Although no organized endochondral ossification appeared to be taking place, there was excessive bone formation at the center of the vertebrae. There was also a generalized increased cellularity of the vertebral cartilage and a corresponding decrease in the abundance of extracellular matrix. The nucleus pulposus of the intervertebral discs were less flattened than in the control mice and possessed an increased amount of large vacuolated cells. Remnants of the notochord could also be seen between adjacent discs.
Hyaluronan production by Has2 is essential for normal vertebral and intervertebral disc development within the spine, and the absence of this synthase impairs the organization of both soft and hard tissue elements.
软骨特异性敲除小鼠脊柱发育的组织学分析。
评估透明质酸合酶-2(Has2)产生的透明质酸在脊柱发育中的作用。
Has2 基因负责全身大部分透明质酸的产生,包括骨骼。然而,使用组成型 Has2 敲除小鼠研究透明质酸在骨骼发育中的作用是不可能的,因为胚胎小鼠在骨骼发育发生之前很早就死亡了。这个问题可以通过使用软骨特异性敲除小鼠来克服。
将带有 floxed Has2 基因的小鼠与在 II 型胶原启动子控制下表达 Cre 重组酶的小鼠杂交,以产生软骨特异性 Has2 敲除小鼠。通过组织学研究脊柱发育。
敲除小鼠在接近出生时死亡,并显示出严重的骨骼发育异常。脊柱在椎体大小和椎间盘形成方面存在缺陷。在椎体中没有证据表明形成有组织的初级骨化中心,并且肥大软骨细胞的形态和组织异常。尽管似乎没有进行有组织的软骨内骨化,但椎体中心有过多的骨形成。椎体软骨的细胞密度普遍增加,细胞外基质的丰度相应减少。椎间盘的髓核没有对照组扁平,并且有大量大空泡细胞。在相邻椎间盘之间还可以看到脊索的残余物。
Has2 产生的透明质酸对于脊柱内正常的椎体和椎间盘发育是必不可少的,这种合成酶的缺失会损害软、硬组织元素的组织。