Department of Physiology, University of Pennsylvania, 3700 Hamilton Walk, Philadelphia, PA, 19104-6085, USA.
Purinergic Signal. 2006 Sep;2(3):499-507. doi: 10.1007/s11302-005-3980-7. Epub 2006 Aug 11.
The purines ATP and adenosine play an important role in the communication between the photoreceptors and the retinal pigment epithelium (RPE). While the RPE is known to release ATP into subretinal space, the source of extracellular adenosine is unclear. In other tissues, ecto-nucleotidases mediate the consecutive dephosphorylation of ATP to AMP, and AMP is converted to adenosine by ecto-5' nucleotidase (CD73). This study identifies ecto-5' nucleotidase on RPE cells and investigates modulation of enzyme activity. The RPE was the most active site of 5'AMP dephosphorylation in the posterior rat eye. The ecto-5' nucleotidase inhibitor alphabetamADP prevented the production adenosine by the apical membrane of the bovine RPE. Cultured human ARPE-19 cells expressed mRNA and protein for ecto-5' nucleotidase. The production of phosphate from 5'AMP by ARPE-19 cells was inhibited by alphabetamADP, but the ecto-alkaline phosphatase inhibitor levamisole had no effect. Degradation of 5'AMP was blocked by norepinephrine, epinephrine and phenylephrine, with inhibition by antagonists prazosin and corynanthine implicating the alpha1 adrenergic receptor. The block of enzyme activity by norepinephrine was rapid, occurring within 1 min, and was similar at both 4 and 37 degrees C, consistent with cleavage of the enzyme from its GPI anchor. HPLC measurements indicated norepinephrine reduced levels of adenosine in the bath. In the apical face of the bovine-RPE eyecup, norepinephrine reduced the production of phosphate from 5'AMP, suggesting that both receptor and enzyme face sub-retinal space. In conclusion, RPE cells express ecto-5' nucleotidase, with activity on the apical membrane, and stimulation of alpha-1 adrenergic receptors downregulates activity. As epinephrine is released at light onset, and adenosine can inhibit phagocytosis, the corresponding decrease in subretinal adenosine levels may contribute to the enhanced the phagocytosis of rod outer segments that occurs at this time.
嘌呤核苷酸 ATP 和腺苷在光感受器和视网膜色素上皮 (RPE) 之间的通讯中发挥重要作用。虽然已知 RPE 将 ATP 释放到视网膜下腔,但细胞外腺苷的来源尚不清楚。在其他组织中,外核苷酸酶介导 ATP 连续去磷酸化为 AMP,然后由外 5'核苷酸酶 (CD73) 将 AMP 转化为腺苷。本研究鉴定了 RPE 细胞上的外 5'核苷酸酶,并研究了酶活性的调节。在大鼠眼后部,RPE 是 5'AMP 去磷酸化最活跃的部位。外核苷酸酶抑制剂alphabetamADP 可阻止牛 RPE 顶膜产生腺苷。培养的人 ARPE-19 细胞表达外 5'核苷酸酶的 mRNA 和蛋白。alphabetamADP 抑制 ARPE-19 细胞从 5'AMP 产生磷酸盐,但外碱性磷酸酶抑制剂左旋咪唑没有作用。去甲肾上腺素、肾上腺素和苯肾上腺素阻断 5'AMP 的降解,拮抗剂哌唑嗪和 Corynanthine 抑制作用表明 alpha1 肾上腺素受体的参与。去甲肾上腺素对酶活性的阻断作用迅速,在 1 分钟内发生,在 4 和 37°C 下相似,与酶从其 GPI 锚定蛋白上的裂解一致。HPLC 测量表明去甲肾上腺素降低了浴液中腺苷的水平。在牛 RPE 眼杯的顶侧,去甲肾上腺素减少了 5'AMP 产生的磷酸盐,表明受体和酶都面向视网膜下腔。总之,RPE 细胞表达外 5'核苷酸酶,其活性位于顶膜上,α-1 肾上腺素受体的刺激可下调其活性。由于肾上腺素在光起始时释放,并且腺苷可以抑制吞噬作用,因此此时视网膜下腺苷水平的相应降低可能有助于增强对杆状细胞外段的吞噬作用。