Pacifici M, Golden E B, Iwamoto M, Adams S L
Department of Anatomy/Histology, School of Dental Medicine, University of Pennsylvania, Philadelphia 19104-6003.
Exp Cell Res. 1991 Jul;195(1):38-46. doi: 10.1016/0014-4827(91)90497-i.
The vitamin A derivative retinoic acid (RA) is widely thought to be involved in cartilage development, but its precise roles and mechanisms of action in this complex process remain unclear. We have tested the hypothesis that RA is involved in chondrocyte maturation during endochondral ossification and, in particular, is an inducer of maturation-associated traits such as type X collagen and alkaline phosphatase. Immature chondrocytes isolated from the caudal region of Day 19 chick embryo sterna were seeded in secondary monolayer cultures and treated either with a high dose (100 nM) or with physiological doses (10-35 nM) of RA for up to 3 days. We found that after an initial lag of about 24 h, physiological doses of RA indeed induced type X collagen gene expression in the immature cells. This induction was not accompanied by obvious changes in expression of the type II collagen and large aggregating proteoglycan core protein genes. As revealed by immunocytochemistry, 30-35% of the cells in cultures treated with RA for 3 days were engaged in type X collagen production. Interestingly, these cells were relatively similar in size to chondrocytes in which no type X collagen was detected, suggesting that chondrocytes can initiate type X collagen production independent of cell hypertrophy. RA treatment also led to increased alkaline phosphatase activity occurring as early as 24 h after the start of treatment. The data in this study indicate that RA may have a role in endochondral ossification as an inducer/promoter of maturation-associated traits during chondrocyte maturation.
维生素A衍生物视黄酸(RA)被广泛认为参与软骨发育,但其在这一复杂过程中的精确作用和作用机制仍不清楚。我们检验了这样一个假设,即RA参与软骨内成骨过程中的软骨细胞成熟,特别是作为诸如X型胶原和碱性磷酸酶等成熟相关特征的诱导剂。从第19天鸡胚胸骨尾端区域分离的未成熟软骨细胞接种于二级单层培养物中,用高剂量(100 nM)或生理剂量(10 - 35 nM)的RA处理长达3天。我们发现,在最初约24小时的延迟后,生理剂量的RA确实诱导了未成熟细胞中X型胶原基因的表达。这种诱导并没有伴随着II型胶原和大聚集蛋白聚糖核心蛋白基因表达的明显变化。免疫细胞化学显示,用RA处理3天的培养物中30 - 35%的细胞参与了X型胶原的产生。有趣的是,这些细胞的大小与未检测到X型胶原的软骨细胞相对相似,这表明软骨细胞可以独立于细胞肥大启动X型胶原的产生。RA处理还导致碱性磷酸酶活性增加,早在处理开始后24小时就出现。本研究中的数据表明,RA可能在软骨内成骨中作为软骨细胞成熟过程中成熟相关特征的诱导剂/促进剂发挥作用。