German Mouse Clinic, Institute of Developmental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health (GmbH), Ingolstädter Landstrasse 1, 85764 Neuherberg, Germany.
Mamm Genome. 2013 Aug;24(7-8):295-302. doi: 10.1007/s00335-013-9470-2. Epub 2013 Aug 9.
Scheimpflug imaging has recently been established for in vivo imaging of the anterior eye segment and quantitative determination of lens transparency in the mouse. This enables more effective investigations of cataract formation with the mouse model, including longitudinal studies. In order to enable recognition of disease-associated irregularities, we performed Scheimpflug measurements with the common laboratory inbred lines C57BL/6J, C3HeB/FeJ, FVB/NCrl, BALB/cByJ, and 129/SvJ in a period between 2 and 12 months of age. C57BL/6J mice showed lowest mean lens densities during the test period. Progressive cortical lens opacification was generally observed, with the earliest onset in C57BBL/6J, C3HeB/FeJ, and 129/SvJ, between 2 and 6 months after birth. Moreover, lenses of these inbred lines developed nuclear opacities. Calculated mean lens density significantly increased between 6 and 12 months of age in all inbred strains except 129/SvJ. Lens densities (and the corresponding standard deviations) of FVB/NCrl and 129/SvJ increased most likely because of differences in the genetic background. Albinism as confounder might be excluded since the albino Balb/cByJ mice are more similar to the C57BL/6J or C3Heb/FeJ mice. We further identified strain-specific anterior lens opacities (C57BL/6J) and cloudy corneal lesions (C57BL/6J, FVB/NCrl, and BALB/cByJ) at later stages. In conclusion, our results indicate that there are lifelong opacification processes in the mouse lens. The highest lens transparency and a dark coat color, which prevents interference from light reflections, make mice with the C57BL/6J background most suitable for cataract research by Scheimpflug imaging. We show that lens densitometry by Scheimpflug imaging in mouse eyes can resolve differences of less than 1 %, making it possible to detect differences in cataract development in different mouse strains, even if they are small.
Scheimpflug 成像技术最近已被用于活体成像前眼部,并定量测定小鼠晶状体的透明度。这使得使用小鼠模型更有效地研究白内障的形成,包括纵向研究。为了能够识别与疾病相关的不规则性,我们对 2 至 12 月龄的 C57BL/6J、C3HeB/FeJ、FVB/NCrl、BALB/cByJ 和 129/SvJ 等常见实验室近交系进行了 Scheimpflug 测量。在测试期间,C57BL/6J 小鼠的平均晶状体密度最低。普遍观察到皮质晶状体混浊逐渐加重,最早在 C57BL/6J、C3HeB/FeJ 和 129/SvJ 中发生,在出生后 2 至 6 个月。此外,这些近交系的晶状体出现核混浊。除 129/SvJ 外,所有近交系的晶状体平均密度在 6 至 12 月龄之间均显著增加。FVB/NCrl 和 129/SvJ 的晶状体密度(和相应的标准差)增加最多,可能是由于遗传背景的差异。由于白化病 Balb/cByJ 小鼠与 C57BL/6J 或 C3Heb/FeJ 小鼠更为相似,因此可以排除白化病作为混杂因素的影响。我们进一步在后期发现了特定于品系的前晶状体混浊(C57BL/6J)和混浊性角膜病变(C57BL/6J、FVB/NCrl 和 BALB/cByJ)。总之,我们的结果表明,小鼠晶状体存在终生混浊过程。C57BL/6J 背景的小鼠具有最高的晶状体透明度和深毛色,可防止光反射的干扰,因此最适合使用 Scheimpflug 成像进行白内障研究。我们表明,Scheimpflug 成像在小鼠眼中的晶状体密度测定可以分辨小于 1%的差异,从而可以检测不同小鼠品系白内障发展的差异,即使差异很小。