Connectomics Research Center, National Tsing Hua University, Hsinchu, Taiwan.
Diabetologia. 2012 Dec;55(12):3252-61. doi: 10.1007/s00125-012-2699-6. Epub 2012 Aug 30.
AIMS/HYPOTHESIS: Sympathetic nerves influence islet hormone levels in the circulation. Insights into islet sympathetic innervation and its remodelling in diabetes may impact future therapeutics. However, standard immunohistochemistry and microtome-based microscopy cannot provide an integral view of the islet neurovascular complex. We prepared transparent islet specimens to investigate the spatial relationship between sympathetic nerves, blood vessels and islet cells in normal, streptozotocin-injected and non-obese diabetic mouse models.
Cardiac perfusion of fluorescent lectin was used to label pancreatic blood vessels. Tyrosine hydroxylase and nuclear staining were used to reveal islet sympathetic innervation and microstructure. Optical clearing (i.e. use of immersion solution to reduce scattering) was applied to enable 3-dimensional confocal microscopy of islets to visualise the sympathetic neurovascular complex in space.
Unlike previously reported morphology, we observed perfusive intra-islet, perivascular sympathetic innervation, in addition to peri-islet contacts of sympathetic nerves with alpha cells and sympathetic fibres encircling the adjacent arterioles. The intra-islet axons became markedly prominent in streptozotocin-injected mice (2 weeks after injection). In non-obese diabetic mice, lymphocytic infiltration remodelled the peri-islet sympathetic axons in early insulitis.
CONCLUSIONS/INTERPRETATION: We have established an imaging approach to reveal the spatial features of mouse islet sympathetic innervation. The neurovascular complex and sympathetic nerve-alpha cell contact suggest that sympathetic nerves modulate islet hormone secretion through blood vessels, in addition to acting directly on alpha cells. In islet injuries, sympathetic nerves undergo different remodelling in response to different pathophysiological cues.
目的/假设:交感神经会影响循环中的胰岛激素水平。深入了解胰岛的交感神经支配及其在糖尿病中的重塑,可能会影响未来的治疗方法。然而,标准的免疫组织化学和切片显微镜检查无法提供胰岛神经血管复合体的整体视图。我们准备了透明的胰岛标本,以研究正常、链脲佐菌素注射和非肥胖型糖尿病小鼠模型中胰岛的交感神经、血管和胰岛细胞之间的空间关系。
荧光凝集素的心脏灌注用于标记胰腺血管。酪氨酸羟化酶和核染色用于揭示胰岛的交感神经支配和微观结构。光学透明化(即使用浸液降低散射)用于实现胰岛的三维共聚焦显微镜检查,以可视化交感神经血管复合体的空间结构。
与之前报道的形态学不同,我们观察到了胰岛内、血管周围的有灌注的交感神经支配,以及胰岛周围交感神经与α细胞的接触,以及环绕相邻小动脉的交感神经纤维。在链脲佐菌素注射的小鼠中(注射后 2 周),胰岛内的轴突变得非常明显。在非肥胖型糖尿病小鼠中,淋巴细胞浸润在早期胰岛炎中重塑了胰岛周围的交感神经轴突。
结论/解释:我们已经建立了一种成像方法来揭示小鼠胰岛交感神经支配的空间特征。神经血管复合体和交感神经-α细胞接触表明,交感神经通过血管调节胰岛激素分泌,除了直接作用于α细胞之外。在胰岛损伤中,交感神经会根据不同的病理生理线索发生不同的重塑。