内质网
生物
细胞凋亡
胞浆
脊髓灰质炎病毒
下调和上调
转录因子
细胞生物学
病毒学
病毒
基因
生物化学
酶
作者
Carmen Mirabelli,Isabelle Pelletier,François Téoulé,Pierre‐Olivier Vidalain,Cynthia Brisac,Frédéric Tangy,Françis Delpeyroux,B Blondel
摘要
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.
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