Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia, PA, USA.
Am J Physiol Cell Physiol. 2010 Apr;298(4):C798-806. doi: 10.1152/ajpcell.00406.2009. Epub 2010 Jan 20.
Aqueous humor is formed by fluid transfer from the ciliary stroma sequentially across the pigmented ciliary epithelial (PE) cells, gap junctions, and nonpigmented ciliary epithelial (NPE) cells. Which connexins (Cx) contribute to PE-NPE gap junctional formation appears species specific. We tested whether small interfering RNA (siRNA) against Cx43 (siCx43) affects bovine PE-NPE communication and whether cAMP affects communication. Native bovine ciliary epithelial cells were studied by dual-cell patch clamping, Lucifer Yellow (LY) transfer, quantitative polymerase chain reaction with reverse transcription (qRT-PCR), and Western immunoblot. qRT-PCR revealed at least 100-fold greater expression for Cx43 than Cx40. siCx43 knocked down target mRNA expression by 55 +/- 7% after 24 h, compared with nontargeting control siRNA (NTC1) transfection. After 48 h, siCx43 reduced Cx43 protein expression and LY transfer. The ratio of fluorescence intensity (R(f)) in recipient to donor cell was 0.47 +/- 0.09 (n = 11) 10 min after whole cell patch formation in couplets transfected with NTC1. siCx43 decreased R(f) by approximately 60% to 0.20 +/- 0.07 (n = 13, P < 0.02). Dibutyryl-cAMP (500 microM) also reduced LY dye transfer by approximately 60%, reducing R(f) from 0.41 +/- 0.05 (n = 15) to 0.17 +/- 0.05 (n = 20) after 10 min. Junctional currents were lowered by approximately 50% (n = 6) after 10-min perfusion with 500 microM dibutyryl-cAMP (n = 6); thereafter, heptanol abolished the currents (n = 5). Preincubation with the PKA inhibitor H-89 (2 microM) prevented cAMP-triggered current reduction (n = 6). We conclude that 1) Cx43, but not Cx40, is a major functional component of bovine PE-NPE gap junctions; and 2) under certain conditions, cAMP may act through PKA to inhibit bovine PE-NPE gap junctional communication.
房水是通过睫状基质中的液体依次穿过色素睫状上皮 (PE) 细胞、间隙连接和非色素睫状上皮 (NPE) 细胞来形成的。哪些连接蛋白 (Cx) 有助于 PE-NPE 间隙连接的形成似乎具有物种特异性。我们测试了针对 Cx43 的小干扰 RNA (siCx43) 是否会影响牛的 PE-NPE 通讯,以及 cAMP 是否会影响通讯。通过双细胞贴附式膜片钳技术、Lucifer Yellow (LY) 转移、反转录定量聚合酶链反应 (qRT-PCR) 和 Western 免疫印迹研究了天然牛睫状上皮细胞。qRT-PCR 显示 Cx43 的表达至少比 Cx40 高 100 倍。与非靶向对照 siRNA (NTC1) 转染相比,siCx43 在 24 小时后将靶 mRNA 表达下调 55 +/- 7%。48 小时后,siCx43 降低了 Cx43 蛋白表达和 LY 转移。在转染 NTC1 的偶联体中,整个细胞膜片钳形成后 10 分钟,受体细胞相对于供体细胞的荧光强度比 (R(f)) 为 0.47 +/- 0.09 (n = 11)。siCx43 将 R(f) 降低了约 60%,至 0.20 +/- 0.07 (n = 13,P < 0.02)。二丁酰环腺苷酸 (500 microM) 也使 LY 染料转移减少约 60%,使 10 分钟后的 R(f) 从 0.41 +/- 0.05 (n = 15) 降至 0.17 +/- 0.05 (n = 20)。用 500 microM 二丁酰环腺苷酸 (n = 6) 灌流 10 分钟后,缝隙连接电流降低约 50% (n = 6);此后,庚醇(n = 5) 消除了电流。PKA 抑制剂 H-89 (2 microM) 的预孵育阻止了 cAMP 触发的电流减少 (n = 6)。我们得出结论:1) Cx43,但不是 Cx40,是牛的 PE-NPE 缝隙连接的主要功能成分;2) 在某些条件下,cAMP 可能通过 PKA 发挥作用抑制牛的 PE-NPE 缝隙连接通讯。