Generic placeholder image

Current Drug Delivery

Editor-in-Chief

ISSN (Print): 1567-2018
ISSN (Online): 1875-5704

The Fate of Exogenous Human HSP70 Introduced into Animal Cells by Different Means

Author(s): Marina Yurinskaya, Olga G. Zatsepina, Maxim G. Vinokurov, Natalia V. Bobkova, David G. Garbuz, Alexei V. Morozov, Dina A. Kulikova, Vladimir A. Mitkevich, Alexander A. Makarov, Sergei Yu. Funikov and Michael B. Evgen’ev

Volume 12, Issue 5, 2015

Page: [524 - 532] Pages: 9

DOI: 10.2174/1567201812666150724094207

Price: $65

Abstract

Over the last decade, it has become evident that in mammals, including humans, heat shock protein 70 (HSP70), apart from its intracellular localization, is found in extracellular space, where it may execute various protective functions. Furthermore, the upregulation of HSP70 family members can be beneficial in the prevention and treatment of various human neurodegenerative diseases and cancer. Here, we demonstrate that recombinant human HSP70 after intranasal administration can penetrate various brain regions of mice in its native form and subsequently undergo rapid degradation. It was also shown that labeled HSP70 added to culture medium of different human and mouse cell lines enters the cells with strikingly different kinetics, which positively correlates with the basic levels of membrane bound Toll-like receptors (TLR) that are characteristic of these cell lines. HSP70 administration does not significantly modulate the level of TLR expression at the protein or RNA level. The degradation of the introduced recombinant HSP70 after entering the cells is likely proteasome-dependent and varies significantly depending on the cells type and origin. These results should be considered when developing HSP70-based therapies.

Keywords: Heat shock proteins, Hsp70, Intranasal administration, UPS, Toll-like receptors.

Graphical Abstract


Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy