scholarly journals Chemical chaperones reverse early suppression of regulatory circuits during unfolded protein response in B cells from common variable immunodeficiency patients

2020 ◽  
Vol 200 (1) ◽  
pp. 73-86 ◽  
Author(s):  
D. Bhatt ◽  
R. C. Stan ◽  
R. Pinhata ◽  
M. Machado ◽  
S. Maity ◽  
...  
2008 ◽  
Vol 45 (10) ◽  
pp. 2990-2997 ◽  
Author(s):  
Juliana S. Kuribayashi ◽  
Cíntia R. Bombardieri ◽  
Gisele V. Baracho ◽  
Júlio Aliberti ◽  
Fabiana S. Machado ◽  
...  

2005 ◽  
Vol 280 (48) ◽  
pp. 39762-39771 ◽  
Author(s):  
Alison H. Skalet ◽  
Jennifer A. Isler ◽  
Leslie B. King ◽  
Heather P. Harding ◽  
David Ron ◽  
...  

2002 ◽  
Vol 277 (50) ◽  
pp. 49047-49054 ◽  
Author(s):  
Jennifer N. Gass ◽  
Nicole M. Gifford ◽  
Joseph W. Brewer

Blood ◽  
2008 ◽  
Vol 111 (4) ◽  
pp. 2280-2289 ◽  
Author(s):  
Dong Yun Lee ◽  
Bill Sugden

The oncogene latent membrane protein 1 (LMP1) of Epstein-Barr virus (EBV) without a ligand drives proliferation of EBV-infected B cells. Its levels vary in cells of clonal populations by more than 100-fold, which leads to multiple distinct activities of the oncogene. At intermediate levels it drives proliferation, and at high levels it inhibits general protein synthesis by inducing phosphorylation of eukaryotic initiation factor 2α (eIF2α). We have found that LMP1 activates PERK to induce phosphorylation of eIF2α, which upregulates activating transcription factor 4 (ATF4) expression. ATF4, in turn, transactivates LMP1's own promoter. LMP1 activates not only PERK but also inositol requiring kinase 1 (IRE1) and ATF6, 3 pathways of the unfolded protein response (UPR). Increasing expression levels of LMP1 induced a dose-dependent increase in IRE1 activity, as measured by its “splicing” of XBP-1. These infected B cells secrete immunoglobins independent of the levels of LMP1, indicating that only a threshold level of XBP-1 is required for the secretion. These findings indicate that LMP1's activation of the UPR is a normal event in a continuum of LMP1's expression that leads both to stimulatory and inhibitory functions and regulates the physiology of EBV-infected B cells in multiple, unexpected modes.


2012 ◽  
Vol 51 (3-4) ◽  
pp. 347-355 ◽  
Author(s):  
Ileana V. Aragon ◽  
Robert A. Barrington ◽  
Suzanne Jackowski ◽  
Kazutoshi Mori ◽  
Joseph W. Brewer

2013 ◽  
Vol 144 (5) ◽  
pp. 989-1000.e6 ◽  
Author(s):  
Stewart Siyan Cao ◽  
Ellen M. Zimmermann ◽  
Brandy–Mengchieh Chuang ◽  
Benbo Song ◽  
Anosike Nwokoye ◽  
...  

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