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一个单一基因将青光眼的硬度与血管系统联系起来。

A single gene connects stiffness in glaucoma and the vascular system.

作者信息

Borrás Teresa

机构信息

Department of Ophthalmology, University of North Carolina School of Medicine, 4109C Neuroscience Research Building CB 7041, 105 Mason Farm Road, Chapel Hill, NC 27599-7041, USA.

出版信息

Exp Eye Res. 2017 May;158:13-22. doi: 10.1016/j.exer.2016.08.022. Epub 2016 Sep 1.

Abstract

Arterial calcification results in arterial stiffness and higher systolic blood pressure. Arterial calcification is prevented by the high expression of the Matrix-Gla gene (MGP) in the vascular smooth muscle cells (VSMC) of the arteries' tunica media. Originally, MGP, a gene highly expressed in cartilage and VSMC, was found to be one of the top expressed genes in the trabecular meshwork. The creation of an Mgp-lacZ Knock-In mouse and the use of mouse genetics revealed that in the eye, Mgp's abundant expression is localized and restricted to glaucoma-associated tissues from the anterior and posterior segments. In particular, it is specifically expressed in the regions of the trabecular meshwork and of the peripapillary sclera that surrounds the optic nerve. Because stiffness in these tissues would significantly alter outflow facility and biomechanical scleral stress in the optic nerve head (ONH), we propose MGP as a strong candidate for the regulation of stiffness in glaucoma. MGP further illustrates the presence of a common function affecting key glaucomatous parameters in the front and back of the eye, and thus offers the possibility for a sole therapeutic target for the disease.

摘要

动脉钙化会导致动脉僵硬和收缩压升高。动脉中膜血管平滑肌细胞(VSMC)中基质γ-羧基谷氨酸蛋白基因(MGP)的高表达可预防动脉钙化。最初,MGP是一种在软骨和VSMC中高表达的基因,被发现是小梁网中表达量最高的基因之一。通过构建Mgp-lacZ基因敲入小鼠并利用小鼠遗传学研究发现,在眼睛中,Mgp的丰富表达定位于并局限于眼前段和后段与青光眼相关的组织。特别是,它在小梁网区域以及围绕视神经的视乳头周围巩膜区域特异性表达。由于这些组织的僵硬会显著改变视神经乳头(ONH)的流出易度和生物力学巩膜应力,我们提出MGP是调节青光眼僵硬的有力候选因素。MGP进一步说明了存在一种影响眼睛前后关键青光眼参数的共同功能,因此为该疾病提供了单一治疗靶点的可能性。

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