Wilmer Eye Institute, The Johns Hopkins University School of Medicine, 400 N. Broadway, Smith Research Building, M035, Baltimore, MD 21287, USA.
J Mol Histol. 2011 Feb;42(1):59-69. doi: 10.1007/s10735-010-9307-1. Epub 2011 Jan 4.
Crystallins are very abundant structural proteins of the lens and are also expressed in other tissues. We have previously reported a spontaneous mutation in the rat βA3/A1-crystallin gene, termed Nuc1, which has a novel, complex, ocular phenotype. The current study was undertaken to compare the expression pattern of this gene during eye development in wild type and Nuc1 rats by in situ hybridization (ISH) and immunohistochemistry (IHC). βA3/A1-crystallin expression was first detected in the eyes of both wild type and Nuc1 rats at embryonic (E) day 12.5 in the posterior portion of the lens vesicle, and remained limited to the lens fibers throughout fetal life. After birth, βA3/A1-crystallin expression was also detected in the neural retina (specifically in the astrocytes and ganglion cells) and in the retinal pigmented epithelium (RPE). This suggested that βA3/A1-crystallin is not only a structural protein of the lens, but has cellular function(s) in other ocular tissues. In summary, expression of βA3/A1-crystallin is controlled differentially in various eye tissues with lens being the site of greatest expression. Similar staining patterns, detected by ISH and IHC, in wild type and Nuc1 animals suggest that functional differences in the protein, rather than changes in mRNA/protein level of expression, likely account for developmental abnormalities in Nuc1.
晶体蛋白是晶状体中非常丰富的结构蛋白,也在其他组织中表达。我们之前报道了大鼠βA3/A1-晶体蛋白基因的自发突变,称为 Nuc1,它具有新颖、复杂的眼部表型。本研究旨在通过原位杂交(ISH)和免疫组织化学(IHC)比较野生型和 Nuc1 大鼠眼发育过程中该基因的表达模式。βA3/A1-晶体蛋白的表达首先在野生型和 Nuc1 大鼠的眼部于胚胎(E)第 12.5 天在晶状体泡的后部分被检测到,并且在整个胎儿期仅限于晶状体纤维。出生后,βA3/A1-晶体蛋白的表达也在神经视网膜(特别是星形胶质细胞和神经节细胞)和视网膜色素上皮(RPE)中被检测到。这表明βA3/A1-晶体蛋白不仅是晶状体的结构蛋白,而且在其他眼部组织中具有细胞功能。总之,βA3/A1-晶体蛋白在各种眼部组织中的表达受到差异调控,其中晶状体是表达最丰富的部位。野生型和 Nuc1 动物中通过 ISH 和 IHC 检测到的相似染色模式表明,可能是蛋白质功能的差异而不是 mRNA/蛋白水平表达的变化导致了 Nuc1 中的发育异常。