Guo Qingqing, AlKendi Abdulla, Jiang Xiaoping, Mittone Alberto, Wang Linbo, Larsson Emanuel, Bravin Alberto, Renström Erik, Fang Xianyong, Zhang Enming
School of Computer Science and Technology, Anhui University, Hefei, China.
Islet Pathophysiology, Department of Clinical Science, Lund University Diabetes Centre, Malmö, Sweden.
Heliyon. 2023 Jan 19;9(2):e13081. doi: 10.1016/j.heliyon.2023.e13081. eCollection 2023 Feb.
The pancreatic islet is a highly structured micro-organ that produces insulin in response to rising blood glucose. Here we develop a label-free and automatic imaging approach to visualize the islets in diabetic rodents by the synchrotron radiation X-ray phase-contrast microtomography (SRμCT) at the ID17 station of the European Synchrotron Radiation Facility. The large-size images (3.2 mm × 15.97 mm) were acquired in the pancreas in STZ-treated mice and diabetic GK rats. Each pancreas was dissected by 3000 reconstructed images. The image datasets were further analysed by a self-developed deep learning method, AA-Net. All islets in the pancreas were segmented and visualized by the three-dimension (3D) reconstruction. After quantifying the volumes of the islets, we found that the number of larger islets (=>1500 μm) was reduced by 2-fold (wt 1004 ± 94 vs GK 419 ± 122, P < 0.001) in chronically developed diabetic GK rat, while in STZ-treated diabetic mouse the large islets were decreased by half (189 ± 33 vs 90 ± 29, P < 0.001) compared to the untreated mice. Our study provides a label-free tool for detecting and quantifying pancreatic islets . It implies the possibility of monitoring the state of pancreatic islets in vivo diabetes without labelling.
胰岛是一种高度结构化的微器官,可根据血糖升高产生胰岛素。在此,我们开发了一种无标记自动成像方法,通过欧洲同步辐射装置ID17站的同步辐射X射线相衬显微断层扫描(SRμCT)对糖尿病啮齿动物的胰岛进行可视化。在经链脲佐菌素(STZ)处理的小鼠和糖尿病GK大鼠的胰腺中获取了大尺寸图像(3.2毫米×15.97毫米)。每个胰腺由3000张重建图像组成。图像数据集通过自主研发的深度学习方法AA-Net进一步分析。通过三维(3D)重建对胰腺中的所有胰岛进行分割和可视化。在对胰岛体积进行量化后,我们发现,在慢性发展的糖尿病GK大鼠中,较大胰岛(=>1500微米)的数量减少了2倍(野生型1004±94 vs GK 419±122,P<0.001),而在经STZ处理的糖尿病小鼠中,与未处理小鼠相比,大胰岛数量减少了一半(189±33 vs 90±29,P<0.001)。我们的研究提供了一种用于检测和量化胰岛的无标记工具。这意味着在不进行标记的情况下监测体内糖尿病状态下胰岛状态的可能性。