Asahina K, Obara M, Yoshizato K
Yoshizato MorphoMatrix Project, ERATO, JRDC, and Developmental Biology Laboratory, Department of Biological Science, Hiroshima University, Higashihiroshima, Hiroshima, Japan.
Dev Dyn. 1999 Sep;216(1):59-71. doi: 10.1002/(SICI)1097-0177(199909)216:1<59::AID-DVDY8>3.0.CO;2-B.
We cloned cDNAs of alpha1(I) and alpha1(II) collagen, and studied their expression profiles in regenerating limbs of newts, Cynops pyrrhogaster. The expression of the alpha1(I) gene was markedly up-regulated at the early bud stage of the blastema. In situ hybridization experiments revealed that the alpha1(I) gene was expressed in not only mesenchymal cells of the blastema, but also the basal cells of the wound epidermis at the wound healing stage when the epidermal basement membrane was absent. This unique expression continued until 21 days (late bud stage), while the basement membrane began to form at 14 days. These results indicate biochemical differences between the wound and normal epidermis, and suggest the direct involvement of the former in the synthesis of blastemal matrices of type I collagen. Actually, immunohistochemistry revealed that type I collagen began to be deposited beneath the wound epidermis at 8 days, and accumulated there and around blastemal mesenchymal cells at 14 to 21 days. Undifferentiated mesenchymal cells associated with the amputated muscle fibers actively expressed the alpha1(I) gene. Mesenchymal cells in the central region of blastemas deposited type I collagen fibers around them. Concomitantly with the appearance of prechondrocytes, the alpha1(II) collagen gene became activated. The present study clearly shows that the expression of the genes of both type I and type II collagen in blastemal cells is temporally and regionally well-regulated in a cooperative manner. Dev Dyn 1999;216:59-71.
我们克隆了α1(I)型和α1(II)型胶原蛋白的cDNA,并研究了它们在东方蝾螈(Cynops pyrrhogaster)再生肢体中的表达谱。α1(I)基因的表达在芽基的早期芽阶段显著上调。原位杂交实验表明,α1(I)基因不仅在芽基的间充质细胞中表达,而且在伤口愈合阶段表皮基底膜缺失时,也在伤口表皮的基底细胞中表达。这种独特的表达持续到21天(晚期芽阶段),而基底膜在14天开始形成。这些结果表明伤口表皮与正常表皮之间存在生化差异,并提示前者直接参与I型胶原蛋白芽基质的合成。实际上,免疫组织化学显示I型胶原蛋白在8天时开始沉积在伤口表皮下方,并在14至21天时在那里以及芽基间充质细胞周围积累。与截肢肌肉纤维相关的未分化间充质细胞积极表达α1(I)基因。芽基中央区域的间充质细胞在其周围沉积I型胶原纤维。随着前软骨细胞的出现,α1(II)型胶原蛋白基因被激活。本研究清楚地表明,芽基细胞中I型和II型胶原蛋白基因的表达在时间和区域上以协同方式受到良好调控。《发育动力学》1999年;216:59 - 71。