Jacob T J
J Physiol. 1983 Aug;341:595-601. doi: 10.1113/jphysiol.1983.sp014826.
Ion-sensitive micro-electrodes were used to measure the levels of intracellular free Ca2+ within the intact amphibian lens. The free [Ca2+] was found to constitute 0.4% of the total lens calcium. The pCa measured at the anterior lens surface was found to 6.59, while that at the posterior was 5.70. An 8-fold anterior/posterior Ca2+ gradient thus exists along the optical axis. The intracellular free Ca2+ could be manipulated by incubating the lens in high-Ca2+ or cA2+-free EGTA Ringer solutions. Raising the intracellular free Ca2+ to 0.22 mM caused lens opacification and cellular uncoupling; the coupling ratio was reduced from 1 in control to 0.41 in high Ca2+.
使用离子敏感微电极测量完整两栖动物晶状体中的细胞内游离Ca2+水平。发现游离[Ca2+]占晶状体总钙的0.4%。在晶状体前表面测得的pCa为6.59,而后表面为5.70。因此,沿光轴存在8倍的前后Ca2+梯度。通过将晶状体置于高Ca2+或无Ca2+的EGTA林格氏溶液中孵育,可以操纵细胞内游离Ca2+。将细胞内游离Ca2+提高到0.22 mM会导致晶状体混浊和细胞解偶联;偶联率从对照中的1降低到高Ca2+中的0.41。