Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts, USA.
Invest Ophthalmol Vis Sci. 2010 Sep;51(9):4549-56. doi: 10.1167/iovs.09-4549.
To evaluate the role of crumbs genes and related epithelial polarity loci in the vertebrate cornea.
The authors used histologic analysis and electron microscopy to evaluate the corneas of zebrafish mutant for a crumbs locus oko meduzy (ome) and in mutants of four other loci, nagie oko (nok), heart and soul (has), mosaic eyes (moe), and ncad (formerly glass onion), that function in the same or related genetic pathways. In parallel, they performed an evaluation of corneas in human carriers of a crumbs gene, CRB1, and mutations using topography and biomicroscopy. The expression of the CRB1 gene in the normal human cornea was examined by polymerase chain reaction (PCR) and immunohistochemical staining.
The corneas of zebrafish mutants display severe abnormalities of the epithelial and stromal layers. The epithelial cells do not properly adhere to each other, and fluid-filled spaces form between them. In addition, the layering of the corneal stroma is poorly formed or absent. The corneas of human carriers of CRB1 mutations display shape deviations compared with what has been observed in normal individuals. A PCR product of the correct size was obtained from normal human corneal samples. Sequence analyses confirmed its identity to be the human CRB1 gene. Immunohistochemical staining using anti-CRB1 yielded positive brown deposits in the human cornea.
crumbs genes play a role in the differentiation of the vertebrate cornea. Corneal defects associated with crumbs gene mutations are very severe in the zebrafish model and, in comparison, appear clinically less pronounced in the human eye.
评估 crumbs 基因及相关上皮极性基因座在脊椎动物角膜中的作用。
作者采用组织学分析和电子显微镜检查评估斑马鱼突变体 oko meduzy(ome)和另外 4 个突变体 nagie oko(nok)、heart and soul(has)、mosaic eyes(moe)和 ncad(原名为 glass onion)的角膜,这些突变体涉及相同或相关的遗传途径。同时,作者平行评估了携带 crumbs 基因 CRB1 突变的人类供体的角膜,采用地形学和生物显微镜进行评估。通过聚合酶链反应(PCR)和免疫组织化学染色检查 CRB1 基因在正常人类角膜中的表达。
斑马鱼突变体的角膜上皮和基质层严重异常。上皮细胞彼此不能正确黏附,其间形成充满液体的间隙。此外,角膜基质的分层形成不良或缺失。CRB1 基因突变携带者的人类角膜显示出与正常个体观察到的形状偏差。从正常的人角膜样本中获得了大小正确的 PCR 产物。序列分析证实其与人 CRB1 基因一致。用抗 CRB1 的免疫组织化学染色在人角膜中产生阳性的棕色沉积物。
crumbs 基因在脊椎动物角膜的分化中起作用。与 crumbs 基因突变相关的角膜缺陷在斑马鱼模型中非常严重,相比之下,在人类眼睛中临床表现不太明显。