Cheung J O P, Grant M E, Jones C J P, Hoyland J A, Freemont A J, Hillarby M C
Wellcome Trust Centre for Cell-Matrix Research, School of Biological Sciences, University of Manchester, Manchester, UK.
J Pathol. 2003 Nov;201(3):496-503. doi: 10.1002/path.1462.
It is widely accepted that growth plate chondrocytes undergo apoptosis when they reach the terminal hypertrophic stage of their differentiation during the process of endochondral ossification in vivo. In this report, an established chondrocyte cell culture model of mammalian endochondral ossification was utilized to investigate the fate of chondrocytes after they had entered hypertrophy in vitro. Fetal bovine epiphyseal chondrocytes were treated with the demethylating agent, 5-azacytidine, for 48 h and then cultured under azacytidine-depleted conditions. There was evidence for apoptosis in azacytidine-treated cells, as demonstrated by nuclear condensation and fragmentation (days 27 and 35) using transmission electron microscopy, and the detection of exposed phosphatidylserine on the plasma membrane surface of apoptotic chondrocytes (day 27) using fluorescence-labelled annexin V. Treated cultures on days 10 and 20 and untreated cultures at all corresponding time-points showed no morphological characteristics of apoptosis. In situ hybridization studies of treated cultures revealed that expression of the apoptotic suppressor, bcl-2, remained consistently high throughout the culture period, whilst the apoptotic inducer, bax, was not expressed until day 23. Quantification of these data showed a gradual shift in the ratio of the expression level of bcl-2 and bax in favour of bax with time in culture, particularly from day 23 onwards. Taken together, the results indicate that azacytidine-treated epiphyseal chondrocytes entered terminal hypertrophy from day 23 onwards in culture and died by apoptosis. This study confirms this culture system as a successful recapitulation of the entire mammalian chondrocyte differentiation pathway, including apoptosis. The culture model will prove valuable for studies of the apoptotic fate of terminally differentiated chondrocytes in the growth plate with a view to providing a better understanding of the underlying mechanisms of skeletal malformations and other pathological disorders such as osteoarthritis.
人们普遍认为,在体内软骨内骨化过程中,生长板软骨细胞在达到终末肥大分化阶段时会发生凋亡。在本报告中,利用已建立的哺乳动物软骨内骨化软骨细胞培养模型,研究软骨细胞在体外进入肥大阶段后的命运。用去甲基化剂5-氮杂胞苷处理胎牛骨骺软骨细胞48小时,然后在无氮杂胞苷的条件下培养。有证据表明,经氮杂胞苷处理的细胞发生了凋亡,透射电子显微镜观察到核浓缩和碎片化(第27天和第35天),荧光标记的膜联蛋白V检测到凋亡软骨细胞膜表面暴露的磷脂酰丝氨酸(第27天)。在第10天和第20天处理的培养物以及所有相应时间点未处理的培养物均未显示凋亡的形态学特征。对处理过的培养物进行原位杂交研究表明,凋亡抑制因子bcl-2在整个培养期内表达一直很高,而凋亡诱导因子bax直到第23天才表达。对这些数据的定量分析表明,随着培养时间的推移,bcl-2和bax表达水平的比值逐渐向有利于bax的方向变化,尤其是从第23天开始。综上所述,结果表明,经氮杂胞苷处理的骨骺软骨细胞在培养中从第23天开始进入终末肥大阶段并通过凋亡死亡。本研究证实该培养系统成功地概括了整个哺乳动物软骨细胞分化途径,包括凋亡。该培养模型对于研究生长板中终末分化软骨细胞的凋亡命运将具有重要价值,有助于更好地理解骨骼畸形和骨关节炎等其他病理疾病的潜在机制。