Norose K, Lo W K, Clark J I, Sage E H, Howe C C
Wistar Institute, Philadelphia, Pennsylvania 19104, USA.
Exp Eye Res. 2000 Sep;71(3):295-307. doi: 10.1006/exer.2000.0884.
SPARC (secreted protein acidic and rich in cysteine) is a matricellular protein involved in cell-matrix interactions. We have shown previously that mice deficient in SPARC develop posterior cortical cataract early in life that progresses to a mature opacity and capsule rupture. To evaluate the primary effects of SPARC deficiency in the lens, we examined the lenses of SPARC-null and wild-type mice by electron microscopy and immunohistochemistry to investigate whether ultrastructural abnormalities occur at the basement membrane (capsule)-lens cell interface in SPARC-null mice. The most notable feature in the lenses of SPARC-null mice, relative to wild-type animals, was the modification of the basal surface of the lens epithelial and fiber cells at the basement membrane (capsule) interface. Electron microscopy revealed numerous filopodial projections of the basal surface of the lens epithelial and fiber cells into the extracellular matrix of the anterior, posterior, and equatorial regions of the lens capsule. In 1 week old precataractous lenses, basal invasive filopodia projecting into the capsule were small and infrequent. Both the size and frequency of these filopodia increased in precataractous 3-4 week old lenses and were prominent in the cataractous 5-6 week old lenses. By rhodamine-phalloidin labeling, we confirmed the presence of basal invasive filopodia projecting into the lens capsule and demonstrated that the projections contained actin filaments. In contrast to the obvious abnormal projections at the interface between the basal surface of the lens epithelial and fiber cells and the lens capsule, the apical and lateral plasma membranes of lens epithelial cells and lens fibers in SPARC-null mice were as smooth as those of wild-type mice. We conclude that the absence of SPARC in the murine lens is associated with a filopodial protrusion of the basal surface of the lens epithelium and differentiating fiber cells into the lens capsule. The altered structures appear prior to the opacification of the lens in the SPARC-null model. These observations are consistent with one or more functions previously proposed for SPARC as a modulator of cell shape and cell-matrix interactions.
SPARC(分泌性酸性富含半胱氨酸蛋白)是一种参与细胞与基质相互作用的基质细胞蛋白。我们之前已经表明,缺乏SPARC的小鼠在生命早期会出现后皮质性白内障,并发展为成熟的混浊和晶状体囊破裂。为了评估SPARC缺乏在晶状体中的主要影响,我们通过电子显微镜和免疫组织化学检查了SPARC基因敲除小鼠和野生型小鼠的晶状体,以研究在SPARC基因敲除小鼠的基底膜(囊膜)-晶状体细胞界面是否发生超微结构异常。与野生型动物相比,SPARC基因敲除小鼠晶状体中最显著的特征是晶状体上皮细胞和纤维细胞在基底膜(囊膜)界面的基底表面发生改变。电子显微镜显示,晶状体上皮细胞和纤维细胞的基底表面有许多丝状伪足突入晶状体囊膜前、后和赤道区域的细胞外基质。在1周龄的白内障前期晶状体中,突入囊膜的基底侵袭性丝状伪足较小且不常见。这些丝状伪足的大小和频率在3-4周龄的白内障前期晶状体中增加,并在5-6周龄的白内障晶状体中很突出。通过罗丹明-鬼笔环肽标记,我们证实了有基底侵袭性丝状伪足突入晶状体囊膜,并证明这些突起含有肌动蛋白丝。与晶状体上皮细胞和纤维细胞基底表面与晶状体囊膜之间界面处明显的异常突起形成对比的是,SPARC基因敲除小鼠晶状体上皮细胞和晶状体纤维的顶端和侧面质膜与野生型小鼠的一样光滑。我们得出结论,小鼠晶状体中SPARC的缺失与晶状体上皮细胞和正在分化的纤维细胞的基底表面向晶状体囊膜的丝状伪足突出有关。在SPARC基因敲除模型中,这些改变的结构在晶状体混浊之前就出现了。这些观察结果与之前提出的SPARC作为细胞形状和细胞-基质相互作用调节剂的一种或多种功能一致。