4.7 Article

HIV Activates the Tyrosine Kinase Hck to Secrete ADAM Protease-Containing Extracellular Vesicles

Journal

EBIOMEDICINE
Volume 28, Issue -, Pages 151-161

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ebiom.2018.01.004

Keywords

Hck; Chronic HIV infection; Nef; ADAM17; Plasma extracellular vesicles; Liver; Hepatocytes; Myeloid cells

Funding

  1. German Science Foundation (DFG) [SFB 643, A9 2012-2015]
  2. Ministry of Education and Research [BMBF: 031L0073A]
  3. Comprehensive Cancer Center (CCC) Erlangen
  4. Emerging Fields Program of the Friedrich-Alexander-University of Erlangen-Nurnberg

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HIV-Nef activates the myeloid cell-typical tyrosine kinase Hck, but its molecular role in the viral life cycle is not entirely understood. We found that HIV plasma extracellular vesicles (HIV pEV) containing/10 proteases and Nef also harbor Hck, and analyzed its role in the context of HIV pEV secretion. Myeloid cells required Hck for the vesicle-associated release of ADAM17. This could be induced by the introduction of Nef and implied that HIV targeted Hck for vesicle-associated ADAM17 secretion from a myeloid compartment. The other contents of HIV-pEV, however, including miRNA and effector protein profiles, as well as the presence of haptoglobin suggested hepatocytes as a possible cellular source. HIV liver tissue analysis supported this assumption, revealing induction of Hck translation, evidence for ADAMprotease activation and HIV infection. Our findings suggest that HIV targets Hck to induce pro-inflammatory vesicles release and identifies hepatocytes as a possible host cell compartment. (c) 2018 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license.

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