A study of red blood cell deformability in diabetic retinopathy using optical tweezers

被引:11
|
作者
Smart, Thomas J. [1 ]
Richards, Christopher J. [1 ]
Bhatnagar, Rhythm [2 ]
Pavesio, Carlos [3 ,4 ]
Agrawal, Rupesh [3 ,4 ,5 ]
Jones, Philip H. [1 ]
机构
[1] UCL, Dept Phys & Astron, London WC1E 6BT, England
[2] UCL, Dept Mech Engn, London WC1E 7JE, England
[3] Moorfields Eye Hosp NHS Fdn Trust, London EC1V 2PD, England
[4] UCL, Inst Ophthalmol, London EC1V 9EL, England
[5] Tan Tock Seng Hosp, Natl Healthcare Grp Eye Inst, Singapore 308433, Singapore
关键词
red blood cells; optical stretching;
D O I
10.1117/12.2191281
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Diabetic retinopathy (DR) is a microvascular complication of diabetes mellitus (DM) in which high blood sugar levels cause swelling, leaking and occlusions in the blood vessels of the retina, often resulting in a loss of sight. The microvascular system requires red blood cells (RBCs) to undergo significant cellular deformation in order to pass through vessels whose diameters are significantly smaller than their own. There is evidence to suggest that DM impairs the deformability of RBCs, and this loss of deformability has been associated with diabetic kidney disease (or nephropathy) - another microvascular complication of DM. However, it remains unclear whether reduced deformability of RBCs correlates with the presence of DR. Here we present an investigation into the deformability of RBCs in patients with diabetic retinopathy using optical tweezers. To extract a value for the deformability of RBCs we use a dual-trap optical tweezers set-up to stretch individual RBCs. RBCs are trapped directly (i.e. without micro-bead handles), so rotate to assume a `side-on' orientation. Video microscopy is used to record the deformation events, and shape analysis software is used to determine parameters such as initial and maximum RBC length, allowing us to calculate the deformability for each RBC. A small decrease in deformability of diabetes cells subject to this stretching protocol is observed when compared to control cells. We also report on initial results on three dimensional imaging of individual RBCs using defocussing microscopy.
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页数:7
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