Yu Hongyou, Ren Yijin, Sandham Andrew, Ren Aishu, Huang Lan, Bai Ding
Department of Orthodontics, University of Groningen, Groningen, The Netherlands.
Angle Orthod. 2009 Mar;79(2):346-52. doi: 10.2319/011508-20.1.
To develop a new cementoblast culture method and to detect bone sialoprotein (BSP) expression in response to high and low mechanical tensile stress in cementoblast in vitro.
Cementoblasts were collected from the roots of newborn bovine teeth and were identified with cementum-derived attachment protein (CAP) antibody 3G9. Cell proliferation was evaluated by MTT [3-(4,5-dimethylthazol-2-yl)-2,5-diphenyl tetrazolium bromide] assay, and mineralization was confirmed by von Kossa staining. Mechanical tensile stress was applied in vitro to the cementoblast with the use of a uniaxial four-point bending system with 2000 or 4000 microstrains, at a frequency of 0.5 Hz for 3, 6, 12, 24, or 36 hours. BSP mRNA level was quantified by real-time quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR).
A large amount of cementoblast was observed to be expressing CAP. Cementoblasts had a proliferation tendency similar to that of osteoblasts but different from that of periodontal ligament (PDL) cells. Cementoblasts had the ability to become mineralized between osteoblasts and PDL cells. The mechanical tensile stress significantly up-regulated BSP mRNA expression, which reached a peak at 24 hours in both 2000 and 4000 microstrain groups (P < .01) and was tenfold and sixfold higher than that of controls, respectively. BSP expression dropped toward baseline levels at 36 hours in both groups.
Mechanical tensile stress up-regulated the expression of BSP. Low mechanical tensile stress induced earlier and more intensive up-regulation of BSP mRNA; this might represent the optimal stimuli for cementoblast activity.
开发一种新的成牙骨质细胞培养方法,并检测体外成牙骨质细胞在高、低机械拉伸应力作用下骨涎蛋白(BSP)的表达。
从新生牛牙齿根部收集成牙骨质细胞,并用牙骨质衍生附着蛋白(CAP)抗体3G9进行鉴定。通过MTT [3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑] 法评估细胞增殖,并用冯·科萨染色法确认矿化情况。使用单轴四点弯曲系统对成牙骨质细胞施加2000或4000微应变的机械拉伸应力,频率为0.5 Hz,持续3、6、12、24或36小时。通过实时定量逆转录聚合酶链反应(qRT-PCR)对BSP mRNA水平进行定量。
观察到大量成牙骨质细胞表达CAP。成牙骨质细胞的增殖趋势与成骨细胞相似,但与牙周膜(PDL)细胞不同。成牙骨质细胞在成骨细胞和PDL细胞之间具有矿化能力。机械拉伸应力显著上调BSP mRNA表达,在2000和4000微应变组中,24小时时均达到峰值(P <.01),分别比对照组高10倍和6倍。两组在36小时时BSP表达均降至基线水平。
机械拉伸应力上调了BSP的表达。低机械拉伸应力诱导BSP mRNA更早、更强烈地上调;这可能代表了成牙骨质细胞活性的最佳刺激因素。