کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6196255 | 1602575 | 2016 | 6 صفحه PDF | دانلود رایگان |
- We show that amyloid beta and phosphorylated tau accumulate in choroidal blood vessels in aged mice.
- Amyloid beta and phosphorylated tau levels are significantly greater in Cfhâ/â mice than controls.
- Compromised outer retinal vascular supply may be a feature of macular degeneration.
Extra-cellular deposition including amyloid beta (Aβ) is a feature of retinal ageing. It has been documented for Bruch's membrane (BM) where Aβ is elevated in complement factor H knockout mice (Cfhâ/â) proposed as a model for age related macular degeneration. However, arterial deposition in choroidal vessels prior to perfusion across BM has not been examined. Aβ is associated with tau phosphorylation and these are linked in blood vessels in Alzheimers Disease where they can drive perivascular pathology. Here we ask if Aβ, tau and phosphorylated tau are features of ageing in choroidal vessels in 12 month C57 BL/6 and Cfhâ/â mice, using immune staining and Western blot analysis.Greater levels of Aβ and phosphorylated tau are found in choroidal vessels in Cfhâ/â mice. Western blot revealed a 40% increase in Aβ in Cfhâ/â over C57 BL/6 mice. Aβ deposits coat around 55% of the luminal wall in Cfhâ/â compared to only about 40% in C57 BL/6. Total tau was similar in both groups, but phosphorylated tau increased by >100% in Cfhâ/â compared to C57 BL/6 and covered >75% of the luminal wall compared to 50% in C57 BL/6. Hence, phosphorylated tau is a marked choroidal feature in this mouse model. Aβ deposition was clumped in Cfhâ/â mice and likely to influence blood flow dynamics. Disturbed flow is associated with atherogenesis and may be related to the accumulation of membrane attack complex recently identified between choroidal vessels in those at high risk of macular degeneration due to complement factor H polymorphisms.
Journal: Experimental Eye Research - Volume 147, June 2016, Pages 138-143