Leitges M, Neidhardt L, Haenig B, Herrmann B G, Kispert A
Abt. Molekulare Embryologie and Abt. Entwicklungsbiologie, Max-Planck-Institut für Immunbiologie, Stübeweg 51, Germany.
Development. 2000 Jun;127(11):2259-67. doi: 10.1242/dev.127.11.2259.
The axial skeleton develops from the sclerotome, a mesenchymal cell mass derived from the ventral halves of the somites, segmentally repeated units located on either side of the neural tube. Cells from the medial part of the sclerotome form the axial perichondral tube, which gives rise to vertebral bodies and intervertebral discs; the lateral regions of the sclerotome will form the vertebral arches and ribs. Mesenchymal sclerotome cells condense and differentiate into chondrocytes to form a cartilaginous pre-skeleton that is later replaced by bone tissue. Uncx4.1 is a paired type homeodomain transcription factor expressed in a dynamic pattern in the somite and sclerotome. Here we show that mice homozygous for a targeted mutation of the Uncx4.1 gene die perinatally and exhibit severe malformations of the axial skeleton. Pedicles, transverse processes and proximal ribs, elements derived from the lateral sclerotome, are lacking along the entire length of the vertebral column. The mesenchymal anlagen for these elements are formed initially, but condensation and chondrogenesis do not occur. Hence, Uncx4.1 is required for the maintenance and differentiation of particular elements of the axial skeleton.
中轴骨骼由生骨节发育而来,生骨节是一种间充质细胞团,源自体节的腹侧半部分,体节是位于神经管两侧的节段性重复单位。生骨节内侧部分的细胞形成中轴软骨膜管,该管产生椎体和椎间盘;生骨节的外侧区域将形成椎弓和肋骨。间充质生骨节细胞浓缩并分化为软骨细胞,形成软骨前体骨骼,随后被骨组织取代。Uncx4.1是一种配对型同源结构域转录因子,在体节和生骨节中以动态模式表达。在此我们表明,Uncx4.1基因靶向突变的纯合小鼠在出生时死亡,并表现出严重的中轴骨骼畸形。源自外侧生骨节的椎弓根、横突和近端肋骨在整个脊柱长度上均缺失。这些结构的间充质原基最初形成,但没有发生浓缩和软骨形成。因此,Uncx4.1是中轴骨骼特定结构维持和分化所必需的。