Dysregulated inter-mitochondrial crosstalk in glioblastoma cells revealed by in situ cryo-electron tomography

Author:

Wang Rui123ORCID,Lei Huan12,Wang Hongxiang4,Qi Lei25,Liu Yu’e6,Liu Yunhui12,Shi Yufeng67,Chen Juxiang4,Shen Qing-Tao123ORCID

Affiliation:

1. Department of Chemical Biology, School of Life Sciences, Southern University of Science and Technology, Shenzhen 518055, China

2. Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, China

3. Institute for Biological Electron Microscopy, Southern University of Science and Technology, Shenzhen 518055, China

4. Department of Neurosurgery, Changhai Hospital, Naval Medical University, Shanghai 200433, China

5. Biomedical Research Center for Structural Analysis, Shandong University, Jinan 250012, China

6. Tongji University Cancer Center, Shanghai Tenth People’s Hospital of Tongji University, School of Medicine, Tongji University, Shanghai 200092, China

7. Center for Brain and Spinal Cord Research, School of Medicine, Tongji University, Shanghai 200092, China

Abstract

Glioblastomas (GBMs) are the most lethal primary brain tumors with limited survival, even under aggressive treatments. The current therapeutics for GBMs are flawed due to the failure to accurately discriminate between normal proliferating cells and distinctive tumor cells. Mitochondria are essential to GBMs and serve as potential therapeutical targets. Here, we utilize cryo-electron tomography to quantitatively investigate nanoscale details of randomly sampled mitochondria in their native cellular context of GBM cells. Our results show that compared with cancer-free brain cells, GBM cells own more inter-mitochondrial junctions of several types for communications. Furthermore, our tomograms unveil microtubule-dependent mitochondrial nanotunnel-like bridges in the GBM cells as another inter-mitochondrial structure. These quantified inter-mitochondrial features, together with other mitochondria-organelle and intra-mitochondrial ones, are sufficient to distinguish GBM cells from cancer-free brain cells under scrutiny with predictive modeling. Our findings decipher high-resolution inter-mitochondrial structural signatures and provide clues for diagnosis and therapeutic interventions for GBM and other mitochondria-related diseases.

Funder

MOST | National Key Research and Development Program of China

NATIONAL SCIENCE FOUNDATION OF CHINA

Shanghai Basic Research Program

Publisher

Proceedings of the National Academy of Sciences

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