| Literature DB >> 27405867 |
Carmen Mirabelli1,2, Isabelle Pelletier1,2, François Téoulé1,2,3, Pierre-Olivier Vidalain4,5, Cynthia Brisac1,3,2, Frédéric Tangy4,5, Francis Delpeyroux1,2, Bruno Blondel1,2.
Abstract
Poliovirus (PV)-induced apoptosis seems to play a major role in central nervous system (CNS) tissue injury, a crucial feature of the pathogenesis of poliomyelitis. We have previously shown that calcium (Ca2+) flux from the endoplasmic reticulum (ER) to the cytosol during PV infection is involved in apoptosis induction in human neuroblastoma cells. We show here that PV infection is associated with a transient upregulation of Herp (homocysteine-induced ER protein), a protein known to promote the degradation of ER-resident Ca2+ channels. Herp gene transcription is controlled by the transcription factor CREB3 (cAMP response element-binding protein 3). We found that the CREB3/Herp pathway limited the increase in cytosolic Ca2+ concentration and apoptosis early in PV infection. This may reduce the extent of PV-induced damage to the CNS during poliomyelitis.Entities:
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Year: 2016 PMID: 27405867 DOI: 10.1099/jgv.0.000544
Source DB: PubMed Journal: J Gen Virol ISSN: 0022-1317 Impact factor: 3.891