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在活体视网膜的最小至最大血管中对单细胞血流进行成像。

Imaging single-cell blood flow in the smallest to largest vessels in the living retina.

机构信息

Institute of Optics, University of Rochester, New York, United States.

Center for Visual Science, University of Rochester, New York, United States.

出版信息

Elife. 2019 May 14;8:e45077. doi: 10.7554/eLife.45077.

Abstract

Tissue light scatter limits the visualization of the microvascular network deep inside the living mammal. The transparency of the mammalian eye provides a noninvasive view of the microvessels of the retina, a part of the central nervous system. Despite its clarity, imperfections in the optics of the eye blur microscopic retinal capillaries, and single blood cells flowing within. This limits early evaluation of microvascular diseases that originate in capillaries. To break this barrier, we use 15 kHz adaptive optics imaging to noninvasively measure single-cell blood flow, in one of the most widely used research animals: the C57BL/6J mouse. Measured flow ranged four orders of magnitude (0.0002-1.55 µL min) across the full spectrum of retinal vessel diameters (3.2-45.8 µm), without requiring surgery or contrast dye. Here, we describe the ultrafast imaging, analysis pipeline and automated measurement of millions of blood cell speeds.

摘要

组织光散射限制了活体哺乳动物深层微血管网络的可视化。哺乳动物眼睛的透明度为视网膜微血管——中枢神经系统的一部分——提供了非侵入式的观察视角。尽管其清晰度很高,但眼睛的光学缺陷会使微小的视网膜毛细血管和流动其中的单个血细胞变得模糊。这限制了对起源于毛细血管的微血管疾病的早期评估。为了突破这一障碍,我们使用 15 kHz 自适应光学成像技术,在最广泛使用的研究动物之一——C57BL/6J 小鼠中,非侵入性地测量单细胞血流。在整个视网膜血管直径(3.2-45.8 µm)范围内,测量的血流范围跨越了四个数量级(0.0002-1.55 µL min),而无需手术或对比染料。在这里,我们描述了超快速成像、分析管道和对数百万个血细胞速度的自动测量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6aa/6516827/99426171e342/elife-45077-fig1.jpg

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