posted on 2018-01-30, 00:00authored byK.N. Son, H.L. Lipton
In mice Theiler’s murine encephalomyelitis virus (TMEV) persists in macrophages that eventually
undergo apoptosis. TMEV infection of macrophages in culture induces apoptosis through the intrinsic
pathway, restricting virus yields. We show that inhibition of TMEV-induced apoptosis leads to phosphorylation
of receptor interacting protein 1 (RIP1), localization of RIP1 and RIP3 to mitochondria, ROS
production independent of MAPK activation and programmed necrosis (necroptosis). Blocking both apoptosis
and necroptosis restored virus yields.
Funding
This work was supported by NIH grant NS065945 and the Modestus Bauer Foundation
History
Publisher Statement
This is the author’s version of a work that was accepted for publication in Virus Research. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Virus Res. 2015. 195: 177-182. DOI: 10.1016/j.virusres.2014.10.017.