Large and small extracellular vesicles released by glioma cells in vitro and in vivo

Abstract

Tumour cells release diverse populations of extracellular vesicles (EVs) ranging in size, molecular cargo, and function. We sought to characterize mRNA and protein content of EV subpopulations released by human glioblastoma (GBM) cells expressing a mutant form of epidermal growth factor receptor (U87EGFRvIII) in vitro and in vivo with respect to size, morphology and the presence of tumour cargo. The two EV subpopulations purified from GBM U87EGFRvIII cancer cells, non‐cancer human umbilical vein endothelial cells (HUVEC; control) and serum of U87EGFRvIII glioma‐bearing mice using differential centrifugation (EVs that sediment at 10,000 × g or 100,000 × g are termed large EVs and small EVs, respectively) were characterized using transmission electron microscopy (TEM), confocal microscopy, nanoparticle tracking analysis (NTA), flow cytometry, immunofluorescence (IF), quantitative‐polymerase chain reaction (qPCR), droplet digital polymerase chain reaction (ddPCR) and micro‐nuclear magnetic resonance (μNMR). We report that both U87EGFRvIII and HUVEC release a similar number of small EVs, but U87EGFRvIII glioma cells alone release a higher number of large EVs compared to non‐cancer HUVEC. The EGFRvIII mRNA from the two EV subpopulations from U87EGFRvIII glioma cells was comparable, while the EGFR protein (wild type + vIII) levels are significantly higher in large EVs. Similarly, EGFRvIII mRNA in large and small EVs isolated from the serum of U87EGFRvIII glioma‐bearing mice is comparable, while the EGFR protein (wild type + vIII) levels are significantly higher in large EVs. Here we report for the first time a direct comparison of large and small EVs released by glioma U87EGFRvIII cells and from serum of U87EGFRvIII glioma‐bearing mice. Both large and small EVs contain tumour‐specific EGFRvIII mRNA and proteins and combining these platforms may be beneficial in detecting rare mutant events in circulating biofluids.

Document Details

Document Type
Pub Defense Publication
Publication Date
Nov 27, 2019
Source ID
10.1080/20013078.2019.1689784

Entities

People

  • Anudeep Yekula
  • Bob Carter
  • Dolores Di Vizio
  • Hakho Lee
  • Huilin Shao
  • Koushik Muralidharan
  • Leonora Balaj
  • Matteo Morello
  • Michael R Freeman
  • Ralph Weissleder
  • Valentina R. Minciacchi
  • Xandra O. Breakefield
  • Xuan Zhang
  • Yongil Park

Organizations

  • Cedars-Sinai Medical Center
  • Center for Systems Biology
  • Defense Advanced Research Projects Agency
  • Division of Cancer Prevention, National Cancer Institute
  • Foundation for Clinical Research in Inflammatory Bowel Disease
  • Harvard Medical School
  • Institute for Basic Science
  • Massachusetts General Hospital
  • National Cancer Institute
  • National Center for Advancing Translational Sciences
  • National Institutes of Health

Tags

Fields of Study

  • Biology

Readers

  • Cellular and Molecular Pathways of Apoptosis.
  • Molecular Photonics/Laser Physics
  • Oncology (Cancer Research).

Technology Areas

  • Biotechnology
  • Biotechnology - Cancer Biotech
  • Microelectronics