Uhlmann Susann, Bringmann Andreas, Uckermann Ortrud, Pannicke Thomas, Weick Michael, Ulbricht Elke, Goczalik Iwona, Reichenbach Andreas, Wiedemann Peter, Francke Mike
Department of Ophthalmology, Eye Clinic, University of Leipzig, Leipzig, Germany.
Invest Ophthalmol Vis Sci. 2003 Sep;44(9):4114-22. doi: 10.1167/iovs.03-0183.
In a rabbit model of retinal detachment, early Müller glial cell reactivity was monitored-specifically, changes in membrane features-to determine whether these changes involve an upregulation of purinergic P2 receptor-mediated responses and whether all or some of these alterations could be blocked by suramin or pyridoxal phosphate 6-azophenyl-2',4'-disulfonic acid (PPADS). In addition, the immune cell reactivity (microglial cells and blood-derived immune cells) was monitored.
A local retinal detachment was induced by subretinal injection of a sodium hyaluronate solution. Three, 24, 48, and 72 hours after surgery, Müller cells were acutely isolated, and patch-clamp records of the whole-cell potassium currents were made. The presence of P2 receptor-mediated responses was determined by measuring extracellular adenosine triphosphate (ATP)-induced membrane current increases, and by recording of ATP-induced calcium responses at the vitreal surface of retinal wholemounts. The density of isolectin B(4)-labeled immune cells was determined in the nerve fiber layer of retinal wholemounts.
Within 24 hours of detachment, Müller cell reactivity was evident. The cells downregulated the density of their inwardly rectifying potassium currents to 60% and 47% of the control value at 48 hours and 72 hours of detachment, respectively. This downregulation was accompanied by an enhanced incidence of cells which showed calcium and current responses after ATP application (control: 14%; 24 hours of detachment: 42%; 72 hours of detachment: 80%). Müller cell hypertrophy was apparent at 48 and 72 hours of detachment. Application of suramin during surgery inhibited the downregulation of potassium currents, but not the elevated responsiveness to extracellular ATP; PPADS had no effect. Suramin also inhibited the inflammatory response that was induced by the surgical procedure and that was apparent by the increased number of immune cells.
Reactive responses of Müller cells occur within 24 hours of detachment. Suramin inhibits several (but not all) reactive glial alterations and therefore may represent one candidate for further investigations in the search for drugs that limit detrimental effects of immune cell activation and Müller cell gliosis during retinal detachment.
在视网膜脱离的兔模型中,监测早期米勒胶质细胞的反应性——具体而言,是膜特征的变化——以确定这些变化是否涉及嘌呤能P2受体介导反应的上调,以及这些改变中的全部或部分是否可被苏拉明或磷酸吡哆醛6-偶氮苯基-2',4'-二磺酸(PPADS)阻断。此外,监测免疫细胞反应性(小胶质细胞和血源性免疫细胞)。
通过视网膜下注射透明质酸钠溶液诱导局部视网膜脱离。术后3、24、48和72小时,急性分离米勒细胞,并进行全细胞钾电流的膜片钳记录。通过测量细胞外三磷酸腺苷(ATP)诱导的膜电流增加以及记录视网膜全层玻璃体表面ATP诱导的钙反应来确定P2受体介导反应的存在。在视网膜全层的神经纤维层中测定异凝集素B(4)标记的免疫细胞密度。
脱离后24小时内,米勒细胞反应性明显。在脱离48小时和72小时时,细胞内向整流钾电流密度分别下调至对照值的60%和47%。这种下调伴随着ATP应用后出现钙和电流反应的细胞发生率增加(对照:14%;脱离24小时:42%;脱离72小时:80%)。在脱离48小时和72小时时,米勒细胞肥大明显。手术期间应用苏拉明可抑制钾电流的下调,但不能抑制对细胞外ATP反应性的升高;PPADS无作用。苏拉明还抑制了手术诱导的炎症反应,免疫细胞数量增加表明了这一点。
米勒细胞的反应性在脱离后24小时内出现。苏拉明抑制了几种(但不是全部)反应性胶质细胞改变,因此可能是进一步研究寻找限制视网膜脱离期间免疫细胞激活和米勒细胞胶质增生有害影响的药物的一个候选药物。