TY - JOUR
T1 - Beyond the surface
T2 - Investigation of tumorsphere morphology using volume electron microscopy
AU - Jadav, Nickhil
AU - Velamoor, Sailakshmi
AU - Huang, Daniel
AU - Cassin, Léna
AU - Hazelton, Niki
AU - Eruera, Alice Roza
AU - Burga, Laura N.
AU - Bostina, Mihnea
N1 - Funding Information:
The authors acknowledge the staff at Otago Micro and Nanoscale Imaging (OMNI) electron microscopy suite, particularly Richard Easingwood and Fátima Espercanca Jorge, for their contribution to this work. The authors also acknowledge the indigenous peoples of Kai Tahu, upon whose traditional ancestral lands our institutions, Ōtakou Whaikahu Waka (University of Otago) and OMNI, stand proudly today.
Publisher Copyright:
© 2023 The Author(s)
PY - 2023/12
Y1 - 2023/12
N2 - The advent of volume electron microscopy (vEM) has provided unprecedented insights into cellular and subcellular organization, revolutionizing our understanding of cancer biology. This study presents a previously unexplored comparative analysis of the ultrastructural disparities between cancer cells cultured as monolayers and tumorspheres. By integrating a robust workflow that incorporates high-pressure freezing followed by freeze substitution (HPF/FS), serial block face scanning electron microscopy (SBF-SEM), manual and deep learning-based segmentation, and statistical analysis, we have successfully generated three-dimensional (3D) reconstructions of monolayer and tumorsphere cells, including their subcellular organelles. Our findings reveal a significant degree of variation in cellular morphology in tumorspheres. We observed the increased prevalence of nuclear envelope invaginations in tumorsphere cells compared to monolayers. Furthermore, we detected a diverse range of mitochondrial morphologies exclusively in tumorsphere cells, as well as intricate cellular interconnectivity within the tumorsphere architecture. These remarkable ultrastructural differences emphasize the use of tumorspheres as a superior model for cancer research due to their relevance to in vivo conditions. Our results strongly advocate for the utilization of tumorsphere cells in cancer research studies, enhancing the precision and relevance of experimental outcomes, and ultimately accelerating therapeutic advancements.
AB - The advent of volume electron microscopy (vEM) has provided unprecedented insights into cellular and subcellular organization, revolutionizing our understanding of cancer biology. This study presents a previously unexplored comparative analysis of the ultrastructural disparities between cancer cells cultured as monolayers and tumorspheres. By integrating a robust workflow that incorporates high-pressure freezing followed by freeze substitution (HPF/FS), serial block face scanning electron microscopy (SBF-SEM), manual and deep learning-based segmentation, and statistical analysis, we have successfully generated three-dimensional (3D) reconstructions of monolayer and tumorsphere cells, including their subcellular organelles. Our findings reveal a significant degree of variation in cellular morphology in tumorspheres. We observed the increased prevalence of nuclear envelope invaginations in tumorsphere cells compared to monolayers. Furthermore, we detected a diverse range of mitochondrial morphologies exclusively in tumorsphere cells, as well as intricate cellular interconnectivity within the tumorsphere architecture. These remarkable ultrastructural differences emphasize the use of tumorspheres as a superior model for cancer research due to their relevance to in vivo conditions. Our results strongly advocate for the utilization of tumorsphere cells in cancer research studies, enhancing the precision and relevance of experimental outcomes, and ultimately accelerating therapeutic advancements.
UR - https://www.scopus.com/pages/publications/85174681574
U2 - 10.1016/j.jsb.2023.108035
DO - 10.1016/j.jsb.2023.108035
M3 - Article
C2 - 37805154
AN - SCOPUS:85174681574
SN - 1047-8477
VL - 215
JO - Journal of Structural Biology
JF - Journal of Structural Biology
IS - 4
M1 - 108035
ER -