UC Berkeley - UCSF Graduate Program in Bioengineering, University of California, Berkeley, CA, USA.
Center for Biological Inspiration in Education and Research (CiBER), University of California, Berkeley, CA, USA.
Exp Eye Res. 2021 Nov;212:108777. doi: 10.1016/j.exer.2021.108777. Epub 2021 Sep 29.
We have investigated how connexin 46 (Cx46) regulates lens stiffness by studying different Cx46 knockout (Cx46KO) mice. A modified muscle lever system was used to determine the lens stiffness of wild-type (WT) and Cx46KO mice at the C57BL/6J (B6) and the 129SvJae (129) strain backgrounds according to total lens displacement at the point of maximum force when fresh lenses were compressed with a maximum of 2 mN of force. In comparison to B6-WT controls, young and old B6-Cx46KO lenses showed 23% and 28% reductions in lens displacement, respectively. Comparing to 129-WT controls, old 129-Cx46KO lenses showed 50% reduction in the lens displacement while young 129-Cx46KO lenses displayed similar displacement. Old B6-Cx46KO and old 129-Cx46KO lenses showed almost identical lens displacement, 128 μm versus 127 μm. Morphological data revealed unique changes of peripheral fiber cell shapes in young B6-WT lenses but not in young B6-Cx46KO, 129-WT and 129-Cx46KO lenses. This work reveals Cx46 deletion increases the lens stiffness in both young and old mice at B6 strain background but only in old mice at 129 strain background which contains intermediate filament CP49 gene deletion. Cx46 impairment increases old mouse lens stiffness and may contribute to the development of presbyopia.
我们研究了缝隙连接蛋白 46(Cx46)如何通过调节晶状体硬度,为此我们研究了不同的 Cx46 敲除(Cx46KO)小鼠。采用改良的肌肉杠杆系统,根据新鲜晶状体在最大力点处的总位移,用最大 2 mN 的力压缩来测定 C57BL/6J(B6)和 129SvJae(129)两种背景下野生型(WT)和 Cx46KO 小鼠的晶状体硬度。与 B6-WT 对照组相比,年轻和年老的 B6-Cx46KO 晶状体的晶状体位移分别减少了 23%和 28%。与 129-WT 对照组相比,年老的 129-Cx46KO 晶状体的晶状体位移减少了 50%,而年轻的 129-Cx46KO 晶状体的晶状体位移则相似。年老的 B6-Cx46KO 和年老的 129-Cx46KO 晶状体的晶状体位移几乎相同,分别为 128 μm 和 127 μm。形态学数据显示,年轻的 B6-WT 晶状体的周边纤维细胞形状发生了独特的变化,而年轻的 B6-Cx46KO、129-WT 和 129-Cx46KO 晶状体则没有。本研究表明,Cx46 缺失增加了 B6 背景下年轻和年老小鼠晶状体的硬度,但仅在包含中间丝 CP49 基因缺失的 129 背景下的年老小鼠中增加。Cx46 功能障碍增加了老年小鼠晶状体的硬度,可能导致老视的发生。