Do Chi-Wai, Peterson-Yantorno Kim, Mitchell Claire H, Civan Mortimer M
Department of Physiology, A303 Richards Bldg, University of Pennsylvania, Philadelphia, PA 19104-6085, USA.
Am J Physiol Cell Physiol. 2004 Oct;287(4):C1003-11. doi: 10.1152/ajpcell.00175.2004. Epub 2004 Jun 9.
The eye's aqueous humor is secreted by a bilayered ciliary epithelium comprising pigmented (PE) and nonpigmented (NPE) epithelial cell layers. Stromal Cl(-) enters the PE cells and crosses gap junctions to the NPE cells for release into the aqueous humor. Maxi-Cl(-) channels are expressed in PE cells, but their physiological significance is unclear. To address this question, excised patches and whole native bovine PE cells were patch clamped, and volume was monitored by calcein fluorescence. In symmetrical 130 mM NaCl, cAMP at the cytoplasmic surface of inside-out patches produced concentration-dependent activation of maxi-Cl(-) channels with a unitary conductance of 272 +/- 2 pS (n = 80). Voltage steps from 0 to +/-80 mV, but not to +/-40 mV, produced rapid channel inactivation consistent with the typical characteristics of maxi-Cl(-) channels. cAMP also activated the maxi-Cl(-) channels in outside-out patches. In both cases, maxi-Cl(-) channels were reversibly inhibited by SITS and 5-nitro-2-(phenylpropylamino)benzoate (NPPB). Decreasing cytoplasmic Cl(-) concentration reduced both open-channel probability and unitary conductance. Similarly, the membrane-permeant 8-bromo-cAMP stimulated outward and inward whole cell currents; the stimulation was larger at higher intracellular Cl(-) concentration. As with unitary currents, cAMP-triggered whole cell currents displayed inactivation at +/-80 but not at +/-40 mV. Moreover, cAMP triggered NPPB-sensitive shrinkage of PE cells. The results suggest that cAMP directly activates maxi-Cl(-) channels of native PE cells that contribute to Cl(-) release particularly from Cl(-)-loaded cells. These cAMP-activated channels provide a potential mechanism for reducing and modulating net aqueous humor secretion by facilitating Cl(-) reabsorption into the ciliary stroma.
眼睛的房水由包含色素上皮(PE)和非色素上皮(NPE)细胞层的双层睫状上皮分泌。基质Cl⁻进入PE细胞并通过缝隙连接进入NPE细胞,然后释放到房水中。大电导Cl⁻通道在PE细胞中表达,但其生理意义尚不清楚。为了解决这个问题,对分离的膜片和完整的天然牛PE细胞进行了膜片钳记录,并通过钙黄绿素荧光监测细胞体积。在对称的130 mM NaCl中,外向膜片胞质表面的cAMP产生浓度依赖性激活大电导Cl⁻通道,单通道电导为272±2 pS(n = 80)。从0到±80 mV的电压阶跃,但不是到±40 mV,会导致通道快速失活,这与大电导Cl⁻通道的典型特征一致。cAMP也激活了外向膜片的大电导Cl⁻通道。在这两种情况下,大电导Cl⁻通道都被4-乙酰胺基-4'-异硫氰酸基芪-2,2'-二磺酸(SITS)和5-硝基-2-(苯丙基氨基)苯甲酸(NPPB)可逆性抑制。降低胞质Cl⁻浓度会降低开放通道概率和单通道电导。同样,膜通透性的8-溴-cAMP刺激外向和内向全细胞电流;在较高的细胞内Cl⁻浓度下刺激更大。与单通道电流一样,cAMP触发的全细胞电流在±80 mV时显示失活,但在±40 mV时不显示。此外,cAMP触发了PE细胞对NPPB敏感的收缩。结果表明,cAMP直接激活天然PE细胞的大电导Cl⁻通道,这些通道有助于Cl⁻的释放,特别是从Cl⁻负载的细胞中释放。这些cAMP激活的通道通过促进Cl⁻重吸收进入睫状基质,为减少和调节房水净分泌提供了一种潜在机制。