Wang L F, Dhir P, Bhatnagar A, Srivastava S K
Department of Human Biological Chemistry and Genetics, University of Texas Medical Branch, Galveston, TX 77555-0647, USA.
Exp Eye Res. 1997 Aug;65(2):267-75. doi: 10.1006/exer.1997.0330.
In this study the contribution of osmotic changes to disintegrative globulization of lens cortical fibers was examined. Single fiber cells were isolated by trypsinization of adult rat lens cortex, and morphological changes elicited by exposure to different external solutions were monitored optically. The survival of the fiber-shaped cells was analysed in accordance with the Weibull distribution. Changes in [Ca2+]i were measured using the fluorescent calcium-sensitive dye-Fluo-3. Exposure of isolated fiber cells to Ringer's solution (containing 2 mm Ca2+) led to an exponential increase in [Ca2+]i with a time constant of 10.2+/-0.8 min, and caused disintegrative globulization in 25+/-4 min (=Tg). The process of globulization as well as the rate of increase in [Ca2+]i was delayed by removing Cl- ions from the external media. Globulization was also delayed by adding 20% bovine serum albumin (Tg=107+/-3 min) or chloride channel inhibitors 5, nitro-2-(3-phenylpropylamino) benzoate (NPPB), dideoxyforskolin, niflumic acid, and tamoxifen. When the fiber cells were suspended in isotonic (280 mm sucrose) HEPES-sucrose (HS) or HEPES-EDTA-sucrose (HES) solution, no globulization was observed for an observation time of 120 min. However, exposure to hypotonic (180 mm) HES solution led to disintegration of fiber cells in 75+/-7 min. Disintegration of the fiber induced by hypotonic HES solution could be delayed by either 0. 05 mm leupeptin (Tg=97+/-6 min) or by pre-loading the fibers with BAPTA (Tg=100+/-4 min). Inhibition of membrane calcium transport by 0.5 mm La3+ had no effect on Tg in hypotonic HES. Addition of 2 mm Ca2+ to HES solution accelerated globulization, and Tg was 57+/-4, 69+/-5 and 102+/-6 min for hypo-, iso- and hyper- tonic solutions, respectively. Transient exposure to calcium also accelerated disintegrative globulization of fiber cells exposed subsequently to HES solution. These results suggest that in ionic media, part of the calcium influx in isolated fiber cells is mediated by the influx of chloride ions. In the absence of other ions, the fiber cells still accumulate calcium, although this calcium influx was independent of medium tonicity. Globulization-induced by hypotonic sucrose solution appears to be mediated by the activation of intracellular proteases and by cell swelling-induced release of calcium from internal stores. Such swelling-mediated disintegrative globulization of fiber cells may be of significance in understanding the cellular basis of diabetic cataracts.
在本研究中,研究了渗透变化对晶状体皮质纤维解体性球化的作用。通过胰蛋白酶消化成年大鼠晶状体皮质分离出单纤维细胞,并通过光学监测暴露于不同外部溶液引起的形态变化。根据威布尔分布分析纤维状细胞的存活率。使用荧光钙敏染料Fluo-3测量[Ca2+]i的变化。将分离的纤维细胞暴露于林格氏溶液(含2 mM Ca2+)导致[Ca2+]i呈指数增加,时间常数为10.2±0.8分钟,并在25±4分钟内(=Tg)引起解体性球化。从外部介质中去除Cl-离子可延迟球化过程以及[Ca2+]i的增加速率。添加20%牛血清白蛋白(Tg = 107±3分钟)或氯通道抑制剂5-硝基-2-(3-苯丙基氨基)苯甲酸(NPPB)、双脱氧佛司可林、尼氟酸和他莫昔芬也可延迟球化。当纤维细胞悬浮在等渗(280 mM蔗糖)HEPES-蔗糖(HS)或HEPES-EDTA-蔗糖(HES)溶液中时,在120分钟的观察时间内未观察到球化。然而,暴露于低渗(180 mM)HES溶液导致纤维细胞在75±7分钟内解体。低渗HES溶液诱导的纤维解体可被0.05 mM亮抑酶肽(Tg = 97±6分钟)或用BAPTA预加载纤维(Tg = 100±4分钟)延迟。0.5 mM La3+对膜钙转运的抑制对低渗HES中的Tg没有影响。向HES溶液中添加2 mM Ca2+加速了球化,低渗、等渗和高渗溶液的Tg分别为57±4、69±5和102±6分钟。短暂暴露于钙也加速了随后暴露于HES溶液的纤维细胞的解体性球化。这些结果表明,在离子介质中,分离的纤维细胞中部分钙内流是由氯离子内流介导的。在没有其他离子的情况下,纤维细胞仍然积累钙,尽管这种钙内流与介质张力无关。低渗蔗糖溶液诱导的球化似乎是由细胞内蛋白酶的激活和细胞肿胀诱导的钙从内部储存释放介导的。这种肿胀介导的纤维细胞解体性球化可能对理解糖尿病性白内障的细胞基础具有重要意义。