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1. 吉林大学 口腔医院 正畸科, 吉林 长春 130021
2. 吉林大学 口腔医院 种植科,吉林 长春,130021
收稿日期:2015-05-09,
修回日期:2015-06-09,
纸质出版日期:2015-07-25
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史瑞新, 周延民, 胡敏等. 低能量激光照射对受张力的成骨细胞周期和胞内Ca<sup>2+</sup>浓度的影响[J]. 光学精密工程, 2015,23(7): 1984-1989
SHI Rui-xin, ZHOU Yan-min, HU Min etc. Effects of low level laser irradiation on cell cycle and intracellular calcium concentration of osteoblastic cells under mechanical strain[J]. Editorial Office of Optics and Precision Engineering, 2015,23(7): 1984-1989
史瑞新, 周延民, 胡敏等. 低能量激光照射对受张力的成骨细胞周期和胞内Ca<sup>2+</sup>浓度的影响[J]. 光学精密工程, 2015,23(7): 1984-1989 DOI: 10.3788/OPE.20152307.1984.
SHI Rui-xin, ZHOU Yan-min, HU Min etc. Effects of low level laser irradiation on cell cycle and intracellular calcium concentration of osteoblastic cells under mechanical strain[J]. Editorial Office of Optics and Precision Engineering, 2015,23(7): 1984-1989 DOI: 10.3788/OPE.20152307.1984.
对成骨样细胞施加了周期性张力
探讨了成骨细胞MG-63受张力时的细胞周期和胞内Ca
2+
浓度的变化规律以及低能量激光照射(LLLI)对此变化规律的影响
揭示了LLLI促进骨形成的机制。实验首先将MG-63细胞随机分成对照组、加力组、激光加力组3组
用流式细胞术检测各组细胞周期。然后
将MG-63细胞分为张力组和激光张力组两组
对胞内Ca
2+
浓度变化进行测定
对2组细胞分别加力0
5
15
30
60 min
再对激光张力组施加激光照射1 min后收取细胞
并用荧光探针Fluo-3-AM测定成骨样细胞内Ca
2+
浓度和Ca
2+
阳性细胞百分比。结果显示:MG-63细胞加载张力后
细胞增殖指数提高
施加LLLI后受力的成骨细胞增殖指数进一步提高。张力引起胞内Ca
2+
浓度增加
变化剧烈
LLLI使变化曲线平缓
且胞内Ca
2+
浓度和Ca
2+
阳性细胞百分比增加。实验结果表明:LLLI可促进受张力的成骨细胞增殖
推测可能是通过调节成骨细胞内Ca
2+
浓度的变化规律和水平来完成的。
The cycle strain was exerted on osteoblastic cells
and the changes of cell cycle and intracellular calcium concentration of osteoblastic MG-63 cells under a mechanical stretching were explored and the effect of Low Level Laser Irradiation (LLLI) on the changed rule was revealed. Firstly
MG-63 cells were divided into 3 groups: control group
strain group and LLLI-strain group
and the cell cycles of these MG-63 cells were measured by a flow cytometry (FCM). Then
the MG-63 cells were divided into 2 groups: strain group and LLLI-strain group
and their intracellular calcium concentration was measured by the FCM and a fluorescent indicator fluo-3/AM at 0
5
15
30 and 60 min under the stretching. However
the LLLI-strain group would receive LLLI for 1 min after the stretching. Experimental results indicate that strain groups present higher proliferation indexes as compared to the control group. The laser-strain groups present higher proliferation index than other two groups. For laser-strain group
the concentration of the intracellular calcium ion increases gently
but that in strain group has increased drastically. It concludes that the LLLI promotes the proliferation of MG-63 cells under the stretching
and it may be achieved by regulating the changed rhythm of concentration of the intracellular Ca
2+
.
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