Hanlon Samuel D, Behzad Ali R, Sakai Lynn Y, Burns Alan R
College of Optometry, University of Houston, Houston, TX, 97204, USA.
Imaging and Characterization Core Lab, King Abdullah University of Science and Technology, Thuwal, Saudi Arabia.
Exp Eye Res. 2015 Mar;132:198-207. doi: 10.1016/j.exer.2015.01.014. Epub 2015 Jan 19.
Elastic tissue was first described well over a hundred years ago and has since been identified in nearly every part of the body. In this review, we examine elastic tissue in the corneal stroma with some mention of other ocular structures which have been more thoroughly described in the past. True elastic fibers consist of an elastin core surrounded by fibrillin microfibrils. However, the presence of elastin fibers is not a requirement and some elastic tissue is comprised of non-elastin-containing bundles of microfibrils. Fibers containing a higher relative amount of elastin are associated with greater elasticity and those without elastin, with structural support. Recently it has been shown that the microfibrils, not only serve mechanical roles, but are also involved in cell signaling through force transduction and the release of TGF-β. A well characterized example of elastin-free microfibril bundles (EFMBs) is found in the ciliary zonules which suspend the crystalline lens in the eye. Through contraction of the ciliary muscle they exert enough force to reshape the lens and thereby change its focal point. It is believed that the molecules comprising these fibers do not turn-over and yet retain their tensile strength for the life of the animal. The mechanical properties of the cornea (strength, elasticity, resiliency) would suggest that EFMBs are present there as well. However, many authors have reported that, although present during embryonic and early postnatal development, EFMBs are generally not present in adults. Serial-block-face imaging with a scanning electron microscope enabled 3D reconstruction of elements in murine corneas. Among these elements were found fibers that formed an extensive network throughout the cornea. In single sections these fibers appeared as electron dense patches. Transmission electron microscopy provided additional detail of these patches and showed them to be composed of fibrils (∼10 nm diameter). Immunogold evidence clearly identified these fibrils as fibrillin EFMBs and EFMBs were also observed with TEM (without immunogold) in adult mammals of several species. Evidence of the presence of EFMBs in adult corneas will hopefully pique an interest in further studies that will ultimately improve our understanding of the cornea's biomechanical properties and its capacity to repair.
弹性组织早在一百多年前就被详细描述过,此后在身体的几乎每个部位都被发现。在本综述中,我们研究角膜基质中的弹性组织,并提及一些过去已有更详尽描述的其他眼部结构。真正的弹性纤维由弹性蛋白核心和原纤维微原纤维环绕组成。然而,弹性纤维的存在并非必要条件,一些弹性组织由不含弹性蛋白的微原纤维束组成。含有相对较多弹性蛋白的纤维具有更大的弹性,而不含弹性蛋白的纤维则提供结构支撑。最近研究表明,微原纤维不仅具有机械作用,还通过力转导和转化生长因子-β(TGF-β)的释放参与细胞信号传导。在悬韧带中可发现一个特征明确的无弹性蛋白微原纤维束(EFMBs)的例子,悬韧带将眼内的晶状体悬吊起来。通过睫状肌的收缩,它们施加足够的力来重塑晶状体,从而改变其焦点。据信,构成这些纤维的分子不会更新换代,但在动物的一生中仍保持其拉伸强度。角膜的机械特性(强度、弹性、弹性恢复能力)表明角膜中也存在EFMBs。然而,许多作者报告称,尽管EFMBs在胚胎期和出生后早期发育阶段存在,但在成年人中通常不存在。利用扫描电子显微镜进行的连续块面成像能够对小鼠角膜中的成分进行三维重建。在这些成分中发现了在整个角膜中形成广泛网络的纤维。在单张切片中,这些纤维表现为电子致密斑。透射电子显微镜提供了这些斑的更多细节,并显示它们由原纤维(直径约10纳米)组成。免疫金标记证据清楚地将这些原纤维鉴定为原纤维蛋白EFMBs,并且在几种成年哺乳动物中也通过透射电子显微镜(无免疫金标记)观察到了EFMBs。成年角膜中存在EFMBs的证据有望激发进一步研究的兴趣,这最终将增进我们对角膜生物力学特性及其修复能力的理解。