Spatial mapping of mitochondrial networks and bioenergetics in lung cancer

Author:

Han Mingqi,Bushong Eric A.,Segawa MayukoORCID,Tiard Alexandre,Wong Alex,Brady Morgan R.,Momcilovic Milica,Wolf Dane M.,Zhang RalphORCID,Petcherski Anton,Madany Matthew,Xu Shili,Lee Jason T.ORCID,Poyurovsky Masha V.,Olszewski Kellen,Holloway TravisORCID,Gomez AdrianORCID,John Maie St.,Dubinett Steven M.ORCID,Koehler Carla M.,Shirihai Orian S.ORCID,Stiles LinseyORCID,Lisberg Aaron,Soatto StefanoORCID,Sadeghi Saman,Ellisman Mark H.ORCID,Shackelford David B.ORCID

Abstract

AbstractMitochondria are critical to the governance of metabolism and bioenergetics in cancer cells1. The mitochondria form highly organized networks, in which their outer and inner membrane structures define their bioenergetic capacity2,3. However, in vivo studies delineating the relationship between the structural organization of mitochondrial networks and their bioenergetic activity have been limited. Here we present an in vivo structural and functional analysis of mitochondrial networks and bioenergetic phenotypes in non-small cell lung cancer (NSCLC) using an integrated platform consisting of positron emission tomography imaging, respirometry and three-dimensional scanning block-face electron microscopy. The diverse bioenergetic phenotypes and metabolic dependencies we identified in NSCLC tumours align with distinct structural organization of mitochondrial networks present. Further, we discovered that mitochondrial networks are organized into distinct compartments within tumour cells. In tumours with high rates of oxidative phosphorylation (OXPHOSHI) and fatty acid oxidation, we identified peri-droplet mitochondrial networks wherein mitochondria contact and surround lipid droplets. By contrast, we discovered that in tumours with low rates of OXPHOS (OXPHOSLO), high glucose flux regulated perinuclear localization of mitochondria, structural remodelling of cristae and mitochondrial respiratory capacity. Our findings suggest that in NSCLC, mitochondrial networks are compartmentalized into distinct subpopulations that govern the bioenergetic capacity of tumours.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Reference44 articles.

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2. Perkins, G. A., Ellisman, M. H. & Fox, D. A. Three-dimensional analysis of mouse rod and cone mitochondrial cristae architecture: bioenergetic and functional implications. Mol. Vis. 9, 60–73 (2003).

3. Cogliati, S. et al. Mitochondrial cristae shape determines respiratory chain supercomplexes assembly and respiratory efficiency. Cell 155, 160–171 (2013).

4. Hensley, C. T. et al. Metabolic heterogeneity in human lung tumors. Cell 164, 681–694 (2016).

5. Weinberg, F. et al. Mitochondrial metabolism and ROS generation are essential for Kras-mediated tumorigenicity. Proc. Natl Acad. Sci. USA 107, 8788–8793 (2010).

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