Department of Molecular & Cellular Physiology, Louisiana State University Health Sciences Center, Shreveport, LA, 71130, USA.
Department of Molecular & Cellular Physiology, Louisiana State University Health Sciences Center, Shreveport, LA, 71130, USA.
Exp Eye Res. 2019 Feb;179:125-131. doi: 10.1016/j.exer.2018.11.012. Epub 2018 Nov 13.
We sought to investigate the effects of diabetes and hyaluronidase on the thickness of the endothelial glycocalyx layer in the mouse retina. In our study, the retinal circulation of diabetic Ins2(Akita) mice and their nondiabetic littermates were observed via intravital microscopy. The endothelial glycocalyx thickness was determined from the infusion of two fluorescently labeled plasma markers, one of which was a high molecular weight rhodamine dextran (MW = 155,000) excluded from the glycocalyx, and the other a more permeable low molecular weight sodium fluorescein (MW = 376). In nondiabetic C57BL/6 mice, the glycocalyx thickness also was evaluated prior to and following infusion of hyaluronidase, an enzyme that can degrade hyaluronic acid on the endothelial surface. A leakage index was used to evaluate the influence of hyaluronidase on the transport of the fluorescent tracers from the plasma into the surrounding tissue, and plasma samples were obtained to measure levels of circulating hyaluronic acid. Both diabetes and hyaluronidase infusion significantly reduced the thickness of the glycocalyx in retinal arterioles (but not in venules), and hyaluronidase increased retinal microvascular leakage of both fluorescent tracers into the surrounding tissue. However, only hyaluronidase infusion (not diabetes) increased circulating plasma levels of hyaluronic acid. In summary, our findings demonstrate that diabetes and hyaluronidase reduce the thickness of the retinal endothelial glycocalyx, in which hyaluronic acid may play a significant role in barrier function.
我们试图研究糖尿病和透明质酸酶对小鼠视网膜内皮糖萼层厚度的影响。在我们的研究中,通过活体显微镜观察糖尿病 Ins2(Akita) 小鼠及其非糖尿病同窝仔鼠的视网膜循环。通过输注两种荧光标记的血浆标记物来确定内皮糖萼层的厚度,其中一种是高分子量 rhodamine dextran(MW=155,000),不能穿过糖萼层,另一种是更具渗透性的低分子量 sodium fluorescein(MW=376)。在非糖尿病 C57BL/6 小鼠中,在输注透明质酸酶(一种可以降解内皮表面透明质酸的酶)之前和之后,也评估了糖萼层的厚度。渗漏指数用于评估透明质酸酶对荧光示踪剂从血浆向周围组织转运的影响,并采集血浆样本以测量循环透明质酸的水平。糖尿病和透明质酸酶输注均显著降低了视网膜小动脉(而非小静脉)中糖萼层的厚度,并且透明质酸酶增加了两种荧光示踪剂向周围组织的视网膜微血管渗漏。然而,只有透明质酸酶输注(而非糖尿病)增加了循环血浆中透明质酸的水平。总之,我们的研究结果表明,糖尿病和透明质酸酶降低了视网膜内皮糖萼层的厚度,其中透明质酸可能在屏障功能中起重要作用。