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作 者:孟宇宏[1] 张金强[2] 宁浩勇[1] 路平[1] 洪柳[1] 刘肖[1] 康筱玲[1] 虞积耀[1] 陆应麟[2]
机构地区:[1]解放军海军总医院病理科,北京100037 [2]军事医学科学院基础医学研究所病理生物学研究室
出 处:《中华病理学杂志》2010年第2期100-105,共6页Chinese Journal of Pathology
摘 要:目的通过研究PAR-1对肺巨细胞癌细胞高、低转移细胞株PLA801D和PLA801C[Ca^2+]i的影响,探讨PAR-1参与调节肺癌细胞转移相关功能的分子机制。方法激光共聚焦显微镜检测PLA801D和PLA801C细胞[Ca^2+]i;将反义和正义PAR-1分别转染至PLA801D(D-)和PLA801C(C+)中;用thrombin和TRAP激活PAR-1,观察PAR-1对D-和C+的[Ca^2+]i影响。结果PLA801D(荧光强度59.55,下同)和PLA801C(35.46)细胞之间的平均[Ca^2+]i差异有统计学意义(P〈0.01)。C+的[Ca^2+]i(45.77)明显高于其对照组CV(35.46,P〈0.05),D-的[Ca^2+]i(48.42)明显低于对照组DV(59.55,P〈0.05)。C+和CV的[Ca^2+]i分别在加入thrombin 80s和100s后荧光强度分别达峰值48.19±9.84和45.64±9.87(P〈0.05);二者均在加入TRAP60s后达峰值,分别为111.31±25.00和52.93±11.21(P〈0.05)。D-和DV的[Ca^2+]i在加入thrombin 60s后达峰值,分别为40.71±5.89和61.07±21.36(P〈0.05),二者均在加入TRAP40s后达峰值,分别为84.98±11.23和102.58±21.48(P〈0.05)。结论PLA801D和PLA801C的转移潜能可能与其细胞的[Ca^2+]i有关。激活PAR-1能够上调PLA801D和PLA801C的细胞内Ca^2+信号。PAR-1促进肺巨细胞癌转移的机制与上调细胞内Ca^2+有关。Objectives To investigate molecular mechanisms of PAR-1 regulation on intracellular Ca^2+ mobilization in lung giant cell carcinoma cells in vitro and its involvement in tumor metastasis. Methods Free intracellular Ca^2+ ([ Ca^2+ ] i ) was measured in lung giant cell carcinoma PLA801C and PLA801D cells by confocal microscopy. Sense and anti-sense PAR-1 expression vectors were transfected into PLA801C (C + )and PLA801D( D - ) cells, respectively. The effects of PAR-1 expression were investigated by thrombin and TRAP-induced mobilization of [ Ca^2+ ] i in the C + and D - cells. Results There were significant differences of the mean values of [ Ca^2+] i between PLAS01D (59.55) and PLA801C cells ( 35.46, P 〈 0.01 ). The mean [ Ca^2+ ] i of C + ceils (45.77) was significantly higher than that of its control CV ceils (35.46, P 〈 0. 05 ), and the mean [ Ca^2+ ] i of D - cells (48.42) was significantly lower than that of its control DV cells(59. 55,P 〈0. 05). The peaks of [ Ca^2+ ] i of C + and CV ceils were 48. 19 ± 9. 84 and 45.64 ± 9.87 ( P 〈 0. 05 ) respectively at 80 s and 100 s after thrombin treatment, but were 111.31 ± 25.00 and 52. 93 ± 11.21 ( P 〈 0. 05 ) respectively at 60 s after TRAP treatment. The peaks of [ Ca^2+ ] i of D- and DV cells were 40. 71 ± 5.89 and 61.07± 21.36 ( P 〈 0. 05 ) respectively at 60 s after thrombin treatment,but were 84. 98±11.23 and 102. 58 ±21.48 ( P 〈 0. 05 ) respectively at 40 s after TRAP treatment. Conclusions The high metastatic potential of PLA801D and PLA801C may be related to [ Ca^2+ ] i of the tumor ceils. PAR-1 may play an important role in the metastasis of lung giant cell carcinoma cells by up-regulating the intracellular Ca^2+.
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