Wang Feng, Wu Xiao-Tao, Zhuang Su-Yang, Wang Yun-Tao, Hong Xing, Zhu Lei, Bao Jun-Ping
Department of Orthopaedics, Affiliated Zhongda Hospital of Southeast University, Nanjing, China.
Asian Spine J. 2011 Jun;5(2):73-81. doi: 10.4184/asj.2011.5.2.73. Epub 2011 May 2.
We performed an ex vivo study to observe cell morphology and viability of human nucleus pulposus (NP) chondrocytes isolated from degenerated intervertebral discs (IVD).
To better understand the biological behavior of NP chondrocytes in monolayer cultures.
Biological repair of IVDs by cell-based therapy has been shown to be feasible in clinical trials. As one of the most promising transplanting seeds, how the isolated NP chondrocytes behavior ex vivo has not been fully understood.
Human NP chondrocytes were harvested from 20 degenerated IVDs and cultured in monolayers. Histological and immunochemistry staining was used to detect cell morphology change. Cell viability was studied by analyzing cell cycle distribution and apoptotic rate in the primary and subculuted cells.
The round or polygonal primary NP chondrocytes had an average adherence time of 7 days and took nearly 31 days to reach 95% confluence. The spindle-shaped P1 NP chondrocytes increased growth kinetics and took about 12 hours to adhere and 6.6 days to get 95% confluent. Immunochemistry staining of collagen II was positive in the cell cytoplasm. Nearly 90% of the confluent NP chondrocytes stayed in G1 phase while 16% underwent apoptosis. No significant difference of the collagen II expression, cell cycle distribution or the apoptosis indices were detected between the primary and subcultured NP chondrocytes.
Human NP chondrocytes undergo significant morphological change in monolayer cultures. Cell cycle distribution pattern and apoptosis index of the cutured NP chondrocytes potentially influence their clinical transplantation or laboratory use.
我们进行了一项体外研究,以观察从退变椎间盘(IVD)分离出的人髓核(NP)软骨细胞的细胞形态和活力。
为了更好地了解单层培养中NP软骨细胞的生物学行为。
基于细胞的疗法对IVD进行生物修复在临床试验中已被证明是可行的。作为最有前景的移植种子之一,分离出的NP软骨细胞在体外的行为尚未得到充分了解。
从20个退变的IVD中获取人NP软骨细胞,并进行单层培养。采用组织学和免疫化学染色检测细胞形态变化。通过分析原代细胞和传代细胞的细胞周期分布及凋亡率来研究细胞活力。
圆形或多边形的原代NP软骨细胞平均贴壁时间为7天,达到95%汇合需要近31天。梭形的P1代NP软骨细胞生长动力学增强,贴壁约需12小时,达到95%汇合需要6.6天。胶原蛋白II的免疫化学染色在细胞质中呈阳性。近90%汇合的NP软骨细胞处于G1期,16%发生凋亡。原代和传代NP软骨细胞之间在胶原蛋白II表达、细胞周期分布或凋亡指数方面未检测到显著差异。
人NP软骨细胞在单层培养中会发生显著的形态变化。培养的NP软骨细胞的细胞周期分布模式和凋亡指数可能会影响其临床移植或实验室应用。