Dlasková Andrea, Spacek Tomás, Santorová Jitka, Plecitá-Hlavatá Lydie, Berková Zuzana, Saudek Frantisek, Lessard Mark, Bewersdorf Joerg, Jezek Petr
Department of Membrane Transport Biophysics, No. 75, Institute of Physiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic.
Biochim Biophys Acta. 2010 Jun-Jul;1797(6-7):1327-41. doi: 10.1016/j.bbabio.2010.02.003. Epub 2010 Feb 6.
Insulin production in pancreatic beta-cells is critically linked to mitochondrial oxidative phosphorylation. Increased ATP production triggered by blood glucose represents the beta-cells' glucose sensor. Type-2 diabetes mellitus results from insulin resistance in peripheral tissues and impaired insulin secretion. Pathology of diabetic beta-cells might be reflected by the altered morphology of mitochondrial network. Its characterization is however hampered by the complexity and density of the three-dimensional (3D) mitochondrial tubular networks in these cell types. Conventional confocal microscopy does not provide sufficient axial resolution to reveal the required details; electron tomography reconstruction of these dense networks is still difficult and time consuming. However, mitochondrial network morphology in fixed cells can also be studied by 4Pi microscopy, a laser scanning microscopy technique which provides an approximately 7-fold improved axial resolution (approximately 100 nm) over conventional confocal microscopy. Here we present a quantitative study of these networks in insulinoma INS-1E cells and primary beta-cells in Langerhans islets. The former were a stably-transfected cell line while the latter were transfected with lentivirus, both expressing mitochondrial matrix targeted redox-sensitive GFP. The mitochondrial networks and their partial disintegration and fragmentation are revealed by carefully created iso-surface plots and their quantitative analysis. We demonstrate that beta-cells within the Langerhans islets from diabetic Goto Kakizaki rats exhibited a more disintegrated mitochondrial network compared to those from control Wistar rats and model insulinoma INS-1E cells. Standardization of these patterns may lead to development of morphological diagnostics for Langerhans islets, for the assessment of beta-cell condition, before their transplantations.
胰腺β细胞中的胰岛素生成与线粒体氧化磷酸化密切相关。血糖引发的ATP生成增加代表了β细胞的葡萄糖传感器。2型糖尿病源于外周组织的胰岛素抵抗和胰岛素分泌受损。糖尿病β细胞的病理状态可能通过线粒体网络形态的改变得以体现。然而,这些细胞类型中三维(3D)线粒体管状网络的复杂性和密度阻碍了对其特征的描述。传统共聚焦显微镜无法提供足够的轴向分辨率来揭示所需的细节;对这些密集网络进行电子断层扫描重建仍然困难且耗时。不过,固定细胞中的线粒体网络形态也可以通过4Pi显微镜进行研究,这是一种激光扫描显微镜技术,与传统共聚焦显微镜相比,其轴向分辨率提高了约7倍(约100纳米)。在此,我们对胰岛素瘤INS-1E细胞和胰岛中的原代β细胞中的这些网络进行了定量研究。前者是稳定转染的细胞系,后者用慢病毒转染,二者均表达靶向线粒体基质的氧化还原敏感型绿色荧光蛋白。通过精心创建的等值面图及其定量分析,揭示了线粒体网络及其部分解体和碎片化情况。我们证明,与对照Wistar大鼠和模型胰岛素瘤INS-1E细胞相比,糖尿病Goto Kakizaki大鼠胰岛中的β细胞线粒体网络解体更为严重。这些模式的标准化可能会推动胰岛形态学诊断方法的发展,用于在胰岛移植前评估β细胞状况。