Berthoud Viviana M, Minogue Peter J, Snabb Joseph I, Dzhashiashvili Yulia, Novak Layne A, Zoltoski Rebecca K, Popko Brian, Beyer Eric C
Department of Pediatrics, University of Chicago, Chicago, IL, USA.
Department of Pediatrics, University of Chicago, Chicago, IL, USA.
Exp Eye Res. 2016 May;146:283-288. doi: 10.1016/j.exer.2016.03.025. Epub 2016 Mar 31.
While connexin46 (Cx46) and connexin50 (Cx50) are crucial for maintaining lens transparency and growth, the contributions of a more recently identified lens fiber connexin, Cx23, are poorly understood. Therefore, we studied the consequences of absence of Cx23 in mouse lenses. Cx23-null mice were generated by homologous Cre recombination. Cx23 mRNA was abundantly expressed in wild type lenses, but not in Cx23-null lenses. The transparency and refractive properties of Cx23-null lenses were similar to wild type lenses when examined by darkfield microscopy. Neither the focusing ability nor the light scattering was altered in the Cx23-null lenses. While both Cx46 and Cx50 localized to appositional fiber cell membranes (as in wild type lenses), their levels were consistently (but not significantly) decreased in homozygous Cx23-null lenses. These results suggest that although Cx23 expression can influence the abundance of the co-expressed lens fiber connexins, heterozygous or homozygous expression of a Cx23-null allele does not alter lens transparency.
虽然连接蛋白46(Cx46)和连接蛋白50(Cx50)对于维持晶状体的透明度和生长至关重要,但人们对最近发现的晶状体纤维连接蛋白Cx23的作用了解甚少。因此,我们研究了小鼠晶状体中缺乏Cx23的后果。通过同源Cre重组产生了Cx23基因敲除小鼠。Cx23 mRNA在野生型晶状体中大量表达,但在Cx23基因敲除晶状体中不表达。通过暗视野显微镜检查时,Cx23基因敲除晶状体的透明度和屈光特性与野生型晶状体相似。Cx23基因敲除晶状体的聚焦能力和光散射均未改变。虽然Cx46和Cx50都定位于相邻的纤维细胞膜(如野生型晶状体),但在纯合Cx23基因敲除晶状体中它们的水平持续(但不显著)降低。这些结果表明,虽然Cx23的表达可以影响共表达的晶状体纤维连接蛋白的丰度,但Cx23基因敲除等位基因的杂合或纯合表达不会改变晶状体的透明度。