Mouse serum exosomal proteomic signature in response to asbestos exposure

Abstract

Asbestos‐induced diseases like fibrosis and mesothelioma are very aggressive, without any treatment options. These diseases are diagnosed only at the terminal stages due to lack of early stage biomarkers. The recent discovery of exosomes as circulating biomarkers led us to look for exosomal biomarkers of asbestos exposure in mouse blood. In our model, mice were exposed to asbestos as a single bolus dose by oropharyngeal aspiration. Fifty‐six days later blood was collected, exosomes were isolated from plasma and characterized and subjected to proteomic analysis using Tandem Mass Tag labeling. We identified many proteins, some of which were more abundant in asbestos exposed mouse serum exosomes, and three selected proteins were validated by immunoblotting. Our study is the first to show that serum exosomal proteomic signatures can reveal some important proteins relevant to asbestos exposure that have the potential to be validated as candidate biomarkers. We hope to extrapolate the positive findings of this study to humans in future studies.

Document Details

Document Type
Pub Defense Publication
Publication Date
Apr 16, 2018
Source ID
10.1002/jcb.26863

Entities

People

  • Arti Shukla
  • Maximilian Macpherson
  • Phillip Munson
  • Stacie Beuschel
  • Ying‐wai Lam

Organizations

  • Foundation for the National Institutes of Health
  • National Institute of General Medical Sciences
  • United States Department of Defense
  • University of Vermont

Tags

Fields of Study

  • Biology

Readers

  • Gulf War Illness and Chronic Multisymptom Illness in Veterans.
  • Immunology
  • Marine Ecological Systems Migration

Technology Areas

  • Biotechnology