Wang Nan, Chintala Shravan K, Fini M Elizabeth, Schuman Joel S
New England Eye Center, Tufts University School of Medicine and the Tufts Center for Vision Research, Boston, Massachusetts 02111, USA.
Invest Ophthalmol Vis Sci. 2003 May;44(5):1977-81. doi: 10.1167/iovs.02-0631.
Elevated intraocular pressure (IOP), the major causal risk factor for glaucoma, often decreases after cataract removal by phacoemulsification ultrasound. In this study, the hypothesis that ultrasound energy propagated through a fluid medium induces a stress response with the potential to lower IOP was investigated.
Normal and glaucomatous trabecular meshwork (TM) cell culture lines were initiated from tissue isolated from human cadaveric eyes or trabeculectomy specimens. Cultured cells were treated for 60 seconds with a phacoemulsification ultrasound probe set to a power of 70%. Activation of the TM cell-specific stress response was assayed by enzyme-linked immunosorbent assay (ELISA) and immunolocalization.
Normal TM cell cultures did not release detectable levels of the stress response protein, IL-1alpha, into their culture medium. In contrast, IL-1alpha was easily detected after treatment with ultrasound energy. Consistent with earlier findings, glaucomatous TM cells produced IL-1alpha constitutively, and the level of expression was increased after treatment with phacoemulsification ultrasound. As was previously demonstrated, the stress-regulated transcription factor NF-kappaB was present in the cytoplasm of normal cells, but in the nucleus of glaucomatous cells. After treatment with ultrasound energy, NF-kappaB translocated to the nucleus in the normal cells. Endothelial leukocyte-adhesion molecule (ELAM)-1 was not detected in normal TM cells, but was constitutively present on glaucomatous TM cells, consistent with findings in previous work. ELAM-1 expression was induced in normal cells by ultrasound treatment.
A potentially IOP-lowering stress response is induced in TM cells by ultrasound. The findings suggest that this response may be induced clinically during cataract removal by phacoemulsification, and may be one mechanism responsible for the reduction in IOP that often follows this procedure.
眼压升高是青光眼的主要致病风险因素,在白内障超声乳化摘除术后通常会降低。在本研究中,探讨了通过流体介质传播的超声能量引发应激反应并有可能降低眼压这一假说。
正常和青光眼性小梁网(TM)细胞系从人尸体眼或小梁切除术标本分离的组织中建立。将培养的细胞用设置为70%功率的超声乳化超声探头处理60秒。通过酶联免疫吸附测定(ELISA)和免疫定位分析TM细胞特异性应激反应的激活情况。
正常TM细胞培养物未向其培养基中释放可检测水平的应激反应蛋白白细胞介素-1α(IL-1α)。相比之下,用超声能量处理后很容易检测到IL-1α。与早期研究结果一致,青光眼性TM细胞组成性产生IL-1α,超声乳化超声处理后表达水平增加。如先前所示,应激调节转录因子核因子κB(NF-κB)存在于正常细胞的细胞质中,但存在于青光眼性细胞的细胞核中。用超声能量处理后,NF-κB在正常细胞中转移至细胞核。正常TM细胞中未检测到内皮白细胞黏附分子(ELAM)-1,但在青光眼性TM细胞中组成性存在,与先前工作中的发现一致。超声处理可诱导正常细胞中ELAM-1的表达。
超声在TM细胞中诱导了一种潜在的降低眼压的应激反应。这些发现表明,这种反应可能在白内障超声乳化摘除术临床过程中被诱导,并且可能是该手术后眼压降低的一种机制。