Krengel S, Götz W, Herken R
Abteilung Histologie, Zentrum Anatomie, Göttingen, Germany.
Anat Embryol (Berl). 1996 Jan;193(1):43-51. doi: 10.1007/BF00186832.
The role of extracellular matrix molecules in ontogenetic differentiation processes is a matter of increasing interest. In cartilage development, type II collagen is suspected of promoting chondrogenic differentiation, since its expression has been demonstrated in a range of precartilaginous tissues of vertebrate species. Up to now, no studies supplying a coherent description of type II collagen expression in the skeletogenesis of human embryos including early embryonic stages have been published. In this work, we examine the temporal and spatial distribution of type II collagen mRNA during vertebral column development in human embryos from 4 to 12 weeks of gestation using non-radioactive in situ hybridization. The onset of gene expression was demonstrable in the 5th week in precartilaginous mesenchymal cells and in notochordal cells. Additionally, we found a weaker hybridization signal in the mesenchymal precursors of the intervertebral discs. In the anlagen of the axial skeleton, type II collagen expression decreased during osteogenic reconstruction in the 11th/12th week, whereas expression continued in the notochordal remnants of the future nuclei pulposi. The results suggest a relatively late occurrence of type II collagen in human vertebral development compared with other vertebrate species. The distribution of gene expression is concordant with a possible role of this molecule in promoting differentiation of mesenchymal cells into chondrocytes. The mechanism of this influence remains to be established.
细胞外基质分子在个体发育分化过程中的作用越来越受到关注。在软骨发育过程中,II型胶原被怀疑促进软骨形成分化,因为在一系列脊椎动物物种的软骨前组织中已证实其表达。到目前为止,尚未发表关于包括早期胚胎阶段在内的人类胚胎骨骼发生过程中II型胶原表达的连贯描述的研究。在这项工作中,我们使用非放射性原位杂交技术,研究了妊娠4至12周的人类胚胎脊柱发育过程中II型胶原mRNA的时空分布。基因表达在第5周时在软骨前间充质细胞和脊索细胞中可被检测到。此外,我们在椎间盘的间充质前体中发现了较弱的杂交信号。在轴骨骼的原基中,II型胶原表达在第11/12周的成骨重建过程中下降,而在未来髓核的脊索残余中继续表达。结果表明,与其他脊椎动物物种相比,人类脊柱发育中II型胶原出现相对较晚。基因表达的分布与该分子在促进间充质细胞向软骨细胞分化中的可能作用一致。这种影响的机制仍有待确定。