Qu Bo, Zhang Jin-song
Department of Ophthalmology, First Affiliated Hospital of China Medical University, Shenyang 110001, China.
Zhonghua Yan Ke Za Zhi. 2003 Jul;39(7):389-94.
To determinate the existence of the inositol 1,4,5-triphosphate receptor (IP(3R)) and the ryanodine receptor (RyR), identify their isoforms and assess their functions during calcium ion concentration modulation in a human epithelial cell line (LEC-B3).
LEC-B3 cell line was defrosted and subcultured, the 3rd passage cells were chosen as object when they became confluent. Then the total cellular RNA was extracted from the cells, the expression of mRNA of IP(3R) and RyR isoforms was analyzed by polymerase chain reaction. Ca(2+) ion changes in the same passage cells were observed and analyzed with laser scanning confocal microscope when acetylcholine (Ach), atropine, caffeine, ryanodine, and procaine were added to the extracellular Ca(2+), Mg(2+) free solutions with ethyleneglycol bis ether tetracetic acid or Ca(2+), Mg(2+) involved solutions.
The IP(3R) isoform I, III and RyR isoform I, III mRNA were expressed, the expression of isoform IP(3R) III > IP(3R)I (P < 0.05); RyR III > RyRI (P < 0.01). 10 micro mol/L Ach, 10 mmol/L caffeine and 50 micro mol/L ryanodine all could induce the intracellular free Ca(2+) concentration increase, but the incubation periods, ranges and lasting time of the increases are different: when Ach acted, the duration of calcium increase in calcium involved solutions was a little longer than in calcium free solutions; the amplitude of calcium oscillations induced by Ach was much higher than caffeine and ryanodine, while the onset of the later is slower than the former. Besides, 1 micro mol/L atropine could block the Ach effects, 50 micro mol/L procaine could inhibit the ryanodine effects.
(1) The IP(3R) and RyR gene transcription coexist in the human lens epithelial cell line: LEC-B3, and their isoforms have specificity. (2) Different agonists can induce different calcium changes. (3)The increase of Ca(2+) concentration induced by caffeine or ryanodine suggested the involvement of both the cyclic adenosine diphosphate ribose and the inositol 1,4,5-triphosphate systems in the regulation of intracellular calcium in LEC-B3, and IP(3R) is more sensitive to free Ca(2+) modulation than RyR.
确定1,4,5-三磷酸肌醇受体(IP(3R))和兰尼碱受体(RyR)的存在,鉴定其亚型,并评估它们在人上皮细胞系(LEC-B3)钙离子浓度调节过程中的功能。
复苏并传代培养LEC-B3细胞系,当第3代细胞汇合时将其作为研究对象。然后从细胞中提取总细胞RNA,通过聚合酶链反应分析IP(3R)和RyR亚型的mRNA表达。当将乙酰胆碱(Ach)、阿托品、咖啡因、兰尼碱和普鲁卡因添加到含有乙二醇双醚四乙酸的无细胞外Ca(2+)、Mg(2+)溶液或含有Ca(2+)、Mg(2+)的溶液中时,用激光扫描共聚焦显微镜观察并分析同一代细胞中Ca(2+)离子的变化。
IP(3R)亚型I、III和RyR亚型I、III的mRNA均有表达,IP(3R)亚型III的表达量>IP(3R)I(P<0.05);RyR III>RyR I(P<0.01)。10μmol/L的Ach、10mmol/L的咖啡因和50μmol/L的兰尼碱均可诱导细胞内游离Ca(2+)浓度升高,但升高的潜伏期、幅度和持续时间不同:当Ach作用时,在含钙溶液中钙升高的持续时间比无钙溶液中略长;Ach诱导的钙振荡幅度远高于咖啡因和兰尼碱,而后者的起效比前者慢。此外,1μmol/L的阿托品可阻断Ach的作用,50μmol/L的普鲁卡因可抑制兰尼碱的作用。
(1)IP(3R)和RyR基因转录在人晶状体上皮细胞系LEC-B3中共存,且它们的亚型具有特异性。(2)不同激动剂可诱导不同的钙变化。(3)咖啡因或兰尼碱诱导的Ca(2+)浓度升高表明环状二磷酸腺苷核糖和1,4,5-三磷酸肌醇系统均参与LEC-B3细胞内钙的调节,且IP(3R)对游离Ca(2+)调节比RyR更敏感。