Mechanisms of nuclear content loading to exosomes

Akira Yokoi, Alejandro Villar-Prados, Paul Allen Oliphint, Jianhua Zhang, Xingzhi Song, Peter DeHoff, Robert Morey, Jinsong Liu, Jason Roszik, Karen Clise-Dwyer, Jared K. Burks, Theresa J. O'Halloran, Louise C. Laurent, Anil K. Sood

Research output: Contribution to journalArticlepeer-review

172 Scopus citations

Abstract

Exosome cargoes are highly varied and include proteins, small RNAs, and genomic DNA (gDNA). The presence of gDNA suggests that different intracellular compartments contribute to exosome loading, resulting in distinct exosome subpopulations. However, the loading of gDNA and other nuclear contents into exosomes (nExo) remains poorly understood. Here, we identify the relationship between cancer cell micronuclei (MN), which are markers of genomic instability, and nExo formation. Imaging flow cytometry analyses reveal that 10% of exosomes derived from cancer cells and <1% of exosomes derived from blood and ascites from patients with ovarian cancer carry nuclear contents. Treatment with genotoxic drugs resulted in increased MN and nExos both in vitro and in vivo. We observed that multivesicular body precursors and exosomal markers, such as the tetraspanins, directly interact with MN. Collectively, this work provides new insights related to nExos, which have implications for cancer biomarker development.

Original languageEnglish (US)
Article numbereaax8849
JournalScience Advances
Volume5
Issue number11
DOIs
StatePublished - Nov 20 2019

ASJC Scopus subject areas

  • General

MD Anderson CCSG core facilities

  • Advanced Technology Genomics Core
  • Bioinformatics Shared Resource
  • Flow Cytometry and Cellular Imaging Facility
  • High Resolution Electron Microscopy Facility
  • Research Animal Support Facility
  • Small Animal Imaging Facility
  • Tissue Biospecimen and Pathology Resource
  • Cytogenetics and Cell Authentication Core
  • Functional Genomics Core
  • Proteomics Facility

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