Ireland M E, Wallace P, Sandilands A, Poosch M, Kasper M, Graw J, Liu A, Maisel H, Prescott A R, Hutcheson A M, Goebel D, Quinlan R A
Department of Anatomy and Cell Biology, Wayne State University School of Medicine, Detroit, Michigan 48201, USA.
Anat Rec. 2000 Jan 1;258(1):25-33. doi: 10.1002/(SICI)1097-0185(20000101)258:1<25::AID-AR3>3.0.CO;2-C.
The early embryonic development and expression patterns of the eye lens specific cytoskeletal proteins, CP49 and CP95, were determined for the chick and were found to be similar in both human and mouse. These proteins, as well as their homologs in other species, are obligate polymerization partners which form unique filamentous structures termed "beaded filaments." CP49 and CP95 appeared as protein products after 3 days of embryonic development in the chick during the elongation of primary fiber cells. Although limited data were obtained for human embryos at these early developmental timepoints, they were consistent with the interpretation that the up-regulation of these lens specific proteins began only after the initiation of lens vesicle closure. In situ hybridization with the mouse lens confirmed that message levels for beaded filament proteins were greatly elevated in differentiating primary fiber cells. Nuclease protection assays established that mRNA levels for CP49 remained relatively constant while CP95 mRNA levels increased once the process of secondary fiber formation was under way. Although present in relatively low abundance, the mRNA for a unique splice variant of CP49, CP49(INS), was also detected early in embryonic development and into adulthood. Peptide-specific antibodies directed against unique predicted sequences were able to confirm the protein expression of CP49(INS) in both embryonic and adult chick lens cells. These data present the first detailed study of the expression of CP49 and CP95 during early lens development. They suggest that the up-regulated expression of CP49 and CP95 could serve as pan-specific markers for all vertebrate lens fiber development.
我们确定了鸡胚胎早期眼睛晶状体特异性细胞骨架蛋白CP49和CP95的发育及表达模式,发现其在人类和小鼠中相似。这些蛋白质以及其他物种中的同源物是专性聚合伙伴,它们形成了称为“串珠状细丝”的独特丝状结构。在鸡胚胎发育3天后,初级纤维细胞伸长期间,CP49和CP95作为蛋白质产物出现。尽管在这些早期发育时间点获得的人类胚胎数据有限,但与这些晶状体特异性蛋白质仅在晶状体泡闭合开始后才上调的解释一致。用小鼠晶状体进行的原位杂交证实,在分化的初级纤维细胞中,串珠状细丝蛋白的信息水平大大升高。核酸酶保护试验表明,CP49的mRNA水平保持相对恒定,而CP95的mRNA水平在次级纤维形成过程开始后增加。尽管丰度相对较低,但在胚胎发育早期直至成年期也检测到了CP49的一种独特剪接变体CP49(INS)的mRNA。针对独特预测序列的肽特异性抗体能够证实CP49(INS)在胚胎期和成年期鸡晶状体细胞中的蛋白表达。这些数据首次详细研究了CP49和CP95在晶状体早期发育过程中的表达。它们表明,CP49和CP95的上调表达可作为所有脊椎动物晶状体纤维发育的泛特异性标志物。