Cao Dejun, Quan Zhengxue, Jiang Dianming, Luo Xiaoji, Zhong Weiyang, Liu Gang
Department of Orthopaedics, the First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, P.R.China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2012 Dec;26(12):1442-7.
To research the transfer of adenovirus human bone morphogenetic protein 4 (Ad-hBMP-4) to human degenerative lumbar intervertebral disc cells in vitro and analyze its effect on the proteoglycan, collagen type II, and Sox9 of intervertebral disc cells.
Identified Ad-hBMP-4 was amplified and detected. Degenerative lumbar intervertebral disc cells were aspirated from the degenerative lumbar intervertebral disc of patients with Modic III level disc protrusion (aged, 27-50 years). The expressing position of collagen type II was identified in the intervertebral disc cells through the laser confocal microscope. The intervertebral disc cells at passage 1 were transfected with Ad-hBMP-4 as experimental group. After 3 and 6 days of transfection, RT-PCR was used to detect the mRNA expressions of proteoglycan, collagen type II, and Sox9, and Western blot to detect the expressions of proteoglycan and collagen type II proteins. Non-transfected cells at passage 1 served as control group.
The virus titer of Ad-hBMP-4 was 5 x 10(6) PFU/mL. No morphological changes in the cells after transfection by Ad-hBMP-4. Collagen type II mainly expressed in the cell cytoplasm. The mRNA expressions of the proteoglycan, collagen type II, and Sox9 in experimental group at 3 and 6 days after transfection were significantly higher than those in control group by RT-PCR (P < 0.05), and the expressions of proteoglycan and collagen type II proteins were significantly higher than those in contorl group by Western blot (P < 0.05). There were significant differences between 3 days and 6 days in experimental group (P < 0.05).
Ad-hBMP-4 could transfect human degenerative lumbar intervertebral cells with high efficiency and promote collagen type II, proteoglycan, and Sox9 expressions. hBMP-4 may play an important role in the repair process during early disc degeneration.
研究腺病毒介导的人骨形态发生蛋白4(Ad-hBMP-4)在体外对人退变腰椎间盘细胞的转染情况,并分析其对椎间盘细胞蛋白聚糖、Ⅱ型胶原蛋白及Sox9的影响。
扩增并检测鉴定后的Ad-hBMP-4。从Modic III级椎间盘突出症患者(年龄27 - 50岁)的退变腰椎椎间盘中抽取退变腰椎间盘细胞。通过激光共聚焦显微镜鉴定椎间盘细胞中Ⅱ型胶原蛋白的表达位置。将第1代椎间盘细胞用Ad-hBMP-4转染作为实验组。转染3天和6天后,采用RT-PCR检测蛋白聚糖、Ⅱ型胶原蛋白及Sox9的mRNA表达,采用蛋白质印迹法检测蛋白聚糖和Ⅱ型胶原蛋白的蛋白表达。未转染的第1代细胞作为对照组。
Ad-hBMP-4的病毒滴度为5×10(6) PFU/mL。Ad-hBMP-4转染后细胞无形态学改变。Ⅱ型胶原蛋白主要表达于细胞质中。RT-PCR结果显示,转染后3天和6天实验组中蛋白聚糖、Ⅱ型胶原蛋白及Sox9的mRNA表达均显著高于对照组(P < 0.05),蛋白质印迹法检测显示实验组中蛋白聚糖和Ⅱ型胶原蛋白的蛋白表达显著高于对照组(P < 0.05)。实验组3天和6天之间有显著差异(P < 0.05)。
Ad-hBMP-4可高效转染人退变腰椎间盘细胞,促进Ⅱ型胶原蛋白、蛋白聚糖及Sox9表达。hBMP-4可能在椎间盘早期退变修复过程中起重要作用。