Shami Gerald, Cheng Delfine, Henriquez Jeffrey, Braet Filip
School of Medical Sciences (Discipline of Anatomy and Histology) - The Bosch Institute, The University of Sydney, NSW 2006, Australia.
School of Medical Sciences (Discipline of Anatomy and Histology) - The Bosch Institute, The University of Sydney, NSW 2006, Australia.
Micron. 2014 Dec;67:20-29. doi: 10.1016/j.micron.2014.06.005. Epub 2014 Jun 24.
Herein, we present a comparative analysis of a variety of chemical and physical fixation protocols for the specific visualisation of the membrane-bound vesicles (MBVs) in the Caco-2 colorectal cancer (CRC) cell line. In so doing, we validated the applicability of specific specimen preparation protocols for the preservation and contrasting of membrane-associated vesicles. Next, by employing the best respective chemical (GOT) and physical (SHPF) fixation methods for the application of transmission electron tomography and modelling we were able to characterise MBVs in three-dimensions and at the nanometer scale. In the second part of this study, we employ a correlative light and electron microscopy (CLEM) approach in order to determine which vesicular compartments are implicated in the uptake of FITC-BSA as a model protein drug. In so doing, we provide a solid foundation for future studies investigating chemotherapeutic drug uptake, transport and fate in cancer cell lines.
在此,我们对多种化学和物理固定方案进行了比较分析,用于在Caco-2结肠直肠癌(CRC)细胞系中特异性可视化膜结合囊泡(MBV)。通过这样做,我们验证了特定标本制备方案在保存和对比膜相关囊泡方面的适用性。接下来,通过采用用于透射电子断层扫描和建模的最佳化学(GOT)和物理(SHPF)固定方法,我们能够在三维和纳米尺度上对MBV进行表征。在本研究的第二部分,我们采用相关光电子显微镜(CLEM)方法,以确定哪些囊泡区室参与了作为模型蛋白药物的FITC-BSA的摄取。通过这样做,我们为未来研究癌细胞系中化疗药物的摄取、运输和命运奠定了坚实的基础。