da Silva J L, Stoltz R A, Dunn M W, Abraham N G, Shibahara S
Rockefeller University, New York 10021, USA.
Curr Eye Res. 1997 Apr;16(4):380-6. doi: 10.1076/ceyr.16.4.380.10695.
The RPE is essential in the maintenance of retinal vasculature homeostasis, since increased cellular expression of heme oxygenase-1 (HO-1) has been implicated as a defense mechanism against oxidative stress. This study was done in an effort to determine the levels of the stress protein (32 kD), HO-1, in retinal pigment epithelium (RPE) cells obtained from diabetic and normal eyes.
We measured the levels of HO-1 in the RPE from eight normal and six diabetic donor eyes. For comparison, HO-1 levels were assayed in RPE cells from four donor eyes with long-standing hypertension. Heme oxygenase-1 mRNA copy number was determined by competitive RT/PCR on various ex vivo samples and on RPE cultured from the same donors. Total RNA (1-200 ng) was reverse-transcribed and then amplified by PCR in the same tube as an internal standard obtained by deleting a 50 bp restriction site from the native HO-1 gene.
Relative to the RPE obtained from control donor eyes, RPE from diabetic donors exhibited significantly decreased levels of HO-1 mRNA. In contrast, no significant difference in the levels of HO-1 mRNA was observed in RPE samples derived from hypertensive donor eyes. The diabetic group showed a range of 340-450 HO-1 mRNA copies/ng of total RNA, as compared to 425-8,000 HO-1 mRNA copies/ng of total RNA in RPE from normal donors and 460-7605 copies/ ng in hypertensive donor eyes.
This study represents initial studies exploring the quantitative expression of heme oxygenase in the RPE human eyes. The decreased expression of HO-1, a stress/heat shock protein, may in the RPE contribute to the vulnerability of the neuroretina to significant metabolic alterations encountered in the diabetic state. This was a limited study; additional screening from different donor eyes will be done in order to establish the relationship between RPE, HO-1 expression and eye diseases in which oxidative stress is believed to be a determinant in the pathophysiology.
视网膜色素上皮(RPE)对于维持视网膜血管系统的稳态至关重要,因为血红素加氧酶-1(HO-1)细胞表达增加被认为是一种对抗氧化应激的防御机制。本研究旨在确定从糖尿病患者和正常人眼中获取的视网膜色素上皮(RPE)细胞中应激蛋白(32 kD)HO-1的水平。
我们测量了8只正常供体眼和6只糖尿病供体眼的RPE中HO-1的水平。作为对照,我们检测了4只患有长期高血压的供体眼的RPE细胞中HO-1的水平。通过竞争性逆转录/聚合酶链反应(RT/PCR)测定各种离体样本以及来自相同供体培养的RPE中血红素加氧酶-1 mRNA的拷贝数。将1 - 200 ng的总RNA进行逆转录,然后在同一管中通过PCR进行扩增,同时以从天然HO-1基因中删除一个50 bp限制性位点获得的片段作为内标。
与从对照供体眼中获取的RPE相比,糖尿病供体眼中的RPE显示HO-1 mRNA水平显著降低。相比之下,高血压供体眼中的RPE样本中HO-1 mRNA水平未观察到显著差异。糖尿病组的HO-1 mRNA拷贝数范围为340 - 450拷贝/ng总RNA,而正常供体眼的RPE中为425 - 8,000拷贝/ng总RNA,高血压供体眼的RPE中为460 - 7605拷贝/ng总RNA。
本研究是探索人眼中RPE细胞血红素加氧酶定量表达的初步研究。应激/热休克蛋白HO-1表达降低可能导致RPE中神经视网膜易受糖尿病状态下显著代谢改变的影响。这是一项有限的研究;将从不同供体眼中进行额外筛查,以建立RPE、HO-1表达与眼部疾病之间的关系,在这些疾病中氧化应激被认为是病理生理学的一个决定因素。