Loty S, Foll C, Forest N, Sautier J M
Laboratoire de Biologie-Odontologie, Université Paris VII, Institut Biomédical des Cordeliers, 15-21, rue de l'Ecole de Médecine, F-75270 06, Paris Cedex, France.
Arch Oral Biol. 2000 Oct;45(10):843-56. doi: 10.1016/s0003-9969(00)00062-5.
The nasal septum is an important centre of endochondral ossification during the development of the facial region. Previous studies have shown that it is possible to recapitulate the differentiation programme of 21-day-old rat nasal chondrocytes in vitro. The purpose now was to investigate, in vitro, the cell condensation phase that represents the earliest morphological event associated with cartilage differentiation in skeletal development. The study focuses on the ability of the cells to form condensations before overt differentiation, with special emphasis on gap-junction expression. The gap-junction protein connexin 43 was localized by indirect immunofluorescence as primarily intracellular and, on day 5, at the condensation stage, as spot-like contacts between cells. Intracellular injection of the permeable dye Lucifer yellow led to the staining of up to 20 neighbouring cells, indicating functional gap junctions and coupling. In contrast, treatment of cultures with the gap-junction blocker glycyrrhetinic acid inhibited dye coupling and reduced cartilage differentiation. Northern blotting of connexin 43 mRNA showed a faint band during the first days of culture, with a striking increase after day 4. In addition, the mRNA of the homeodomain-containing gene Cart-1 began to be expressed in prechondrogenic condensations and corresponded to the expression of type II collagen mRNA. These data indicate that the early stage of in vitro chondrocyte differentiation is the formation of cell condensations and the ability to establish cell-to-cell communication. Connexin 43, together with other molecular mechanisms, mediates the condensation phase of chondrogenesis and sets up the optimal environment in which nasal septal cells may terminally differentiate into chondrocytes.
鼻中隔是面部区域发育过程中软骨内骨化的重要中心。先前的研究表明,在体外可以重现21日龄大鼠鼻软骨细胞的分化程序。现在的目的是在体外研究细胞凝聚阶段,这是骨骼发育中与软骨分化相关的最早形态学事件。该研究聚焦于细胞在明显分化之前形成凝聚的能力,特别强调缝隙连接的表达。缝隙连接蛋白连接蛋白43通过间接免疫荧光定位,主要位于细胞内,在第5天的凝聚阶段,表现为细胞间的点状接触。向细胞内注射可渗透染料路西法黄可使多达20个相邻细胞染色,表明存在功能性缝隙连接和细胞偶联。相比之下,用缝隙连接阻滞剂甘草次酸处理培养物可抑制染料偶联并减少软骨分化。连接蛋白43 mRNA的Northern印迹分析显示,培养的最初几天有一条 faint 条带,第4天后显著增加。此外,含同源结构域的基因Cart-1的mRNA开始在软骨前凝聚物中表达,并与II型胶原mRNA的表达相对应。这些数据表明,体外软骨细胞分化的早期阶段是细胞凝聚的形成以及建立细胞间通讯的能力。连接蛋白43与其他分子机制一起,介导软骨形成的凝聚阶段,并建立鼻中隔细胞最终分化为软骨细胞的最佳环境。