Author
Listed:
- Mingqi Han
(University of California Los Angeles (UCLA))
- Eric A. Bushong
(University of California San Diego (UCSD)
UCSD)
- Mayuko Segawa
(University of Cambridge)
- Alexandre Tiard
(UCLA)
- Alex Wong
(Yale University)
- Morgan R. Brady
(University of California Los Angeles (UCLA))
- Milica Momcilovic
(University of California Los Angeles (UCLA))
- Dane M. Wolf
(University of Cambridge
Imperial College)
- Ralph Zhang
(University of California Los Angeles (UCLA))
- Anton Petcherski
(DGSOM UCLA)
- Matthew Madany
(University of California San Diego (UCSD)
UCSD)
- Shili Xu
(UCLA
UCLA
UCLA)
- Jason T. Lee
(UCLA
UCLA
UCLA
Stanford University)
- Masha V. Poyurovsky
(Kadmon Corporation)
- Kellen Olszewski
(Kadmon Corporation)
- Travis Holloway
(UCLA)
- Adrian Gomez
(UCLA)
- Maie St. John
(UCLA
DGSOM UCLA)
- Steven M. Dubinett
(University of California Los Angeles (UCLA)
UCLA
UCLA
DGSOM UCLA)
- Carla M. Koehler
(UCLA
UCLA)
- Orian S. Shirihai
(DGSOM UCLA
UCLA
UCLA)
- Linsey Stiles
(DGSOM UCLA
UCLA)
- Aaron Lisberg
(UCLA
DGSOM UCLA)
- Stefano Soatto
(UCLA)
- Saman Sadeghi
(McMaster University)
- Mark H. Ellisman
(University of California San Diego (UCSD)
UCSD)
- David B. Shackelford
(University of California Los Angeles (UCLA)
UCLA)
Abstract
Mitochondria 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.
Suggested Citation
Mingqi Han & Eric A. Bushong & Mayuko Segawa & Alexandre Tiard & Alex Wong & Morgan R. Brady & Milica Momcilovic & Dane M. Wolf & Ralph Zhang & Anton Petcherski & Matthew Madany & Shili Xu & Jason T. , 2023.
"Spatial mapping of mitochondrial networks and bioenergetics in lung cancer,"
Nature, Nature, vol. 615(7953), pages 712-719, March.
Handle:
RePEc:nat:nature:v:615:y:2023:i:7953:d:10.1038_s41586-023-05793-3
DOI: 10.1038/s41586-023-05793-3
Download full text from publisher
As the access to this document is restricted, you may want to search for a different version of it.
Citations
Citations are extracted by the
CitEc Project, subscribe to its
RSS feed for this item.
Cited by:
- Lin-Lin Zhou & Tao Zhang & Yun Xue & Chuan Yue & Yihui Pan & Pengyu Wang & Teng Yang & Meixia Li & Hu Zhou & Kan Ding & Jianhua Gan & Hongbin Ji & Cai-Guang Yang, 2023.
"Selective activator of human ClpP triggers cell cycle arrest to inhibit lung squamous cell carcinoma,"
Nature Communications, Nature, vol. 14(1), pages 1-15, December.
- Güneş Parlakgül & Song Pang & Leonardo L. Artico & Nina Min & Erika Cagampan & Reyna Villa & Renata L. S. Goncalves & Grace Yankun Lee & C. Shan Xu & Gökhan S. Hotamışlıgil & Ana Paula Arruda, 2024.
"Spatial mapping of hepatic ER and mitochondria architecture reveals zonated remodeling in fasting and obesity,"
Nature Communications, Nature, vol. 15(1), pages 1-18, December.
- Kei, Yik Lun & Chen, Yanzhen & Madrid Padilla, Oscar Hernan, 2023.
"A partially separable model for dynamic valued networks,"
Computational Statistics & Data Analysis, Elsevier, vol. 187(C).
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:nature:v:615:y:2023:i:7953:d:10.1038_s41586-023-05793-3. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.