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Near infrared optical projection tomography for assessments of beta-cell mass distribution in diabetes research

机译:近红外光学投影层析成像技术用于评估糖尿病研究中β细胞的质量分布

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摘要

By adapting OPT to include the capability of imaging in the near infrared (NIR) spectrum, we here illustrate the possibility to image larger bodies of pancreatic tissue, such as the rat pancreas, and to increase the number of channels (cell types) that may be studied in a single specimen. We further describe the implementation of a number of computational tools that provide: 1/ accurate positioning of a specimen's (in our case the pancreas) centre of mass (COM) at the axis of rotation (AR)2; 2/ improved algorithms for post-alignment tuning which prevents geometric distortions during the tomographic reconstruction2 and 3/ a protocol for intensity equalization to increase signal to noise ratios in OPT-based BCM determinations3. In addition, we describe a sample holder that minimizes the risk for unintentional movements of the specimen during image acquisition. Together, these protocols enable assessments of BCM distribution and other features, to be performed throughout the volume of intact pancreata or other organs (e.g. in studies of islet transplantation), with a resolution down to the level of individual islets of Langerhans.
机译:通过使OPT适应近红外(NIR)光谱成像的能力,我们在此说明了对较大的胰腺组织(例如大鼠胰腺)成像的可能性,并增加了可能的成像通道数量(细胞类型)在单个样本中进行研究。我们进一步描述了许多计算工具的实现,这些工具提供:1 /在旋转轴(AR)2上精确定位标本(在我们的情况下为胰腺)质心(COM)2; 2 /用于对齐后调整的改进算法,可防止在断层扫描重建过程中出现几何失真2和3 /用于强度均衡的协议,可提高基于OPT的BCM确定中的信噪比3。此外,我们介绍了一种样品架,可以最大程度地减少图像采集过程中标本意外移动的风险。这些协议共同使评估BCM分布和其他特征的能力得以在完整的胰脏或其他器官的整个体积中进行(例如,在胰岛移植的研究中),分辨率低至朗格罕岛的单个胰岛水平。

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