Mycobacterium tuberculosis PE_PGRS1 promotes mycobacteria intracellular survival via reducing the concentration of intracellular free Ca2+ and suppressing endoplasmic reticulum stress
Xi Yu, Yu Huang, Yuzhu Li, Tongxin Li, Shuangquan Yan, Xuefeng Ai, Xi Lv, Lin Fan, Jianping Xie
Journal:MOLECULAR IMMUNOLOGY
IF:4.17
DOI:10.1016/j.molimm.2022.12.007
PMID:36584479
Published:2022-12-28
research field:细胞生物学免疫学微生物学
Abstract
Mycobacterium tuberculosis ( M. tuberculosis ) is the causative agent of tuberculosis (TB). And the PE_PGRS family members of M. tuberculosis are closely associated with virulence and antigen presentation but with function largely elusive. PE_PGRS1( Rv0109 ) contained 7 Ca 2+ binding domains of GGXGXD/NXUX (X is any amino acid), which can reduce intracellular Ca 2+ surge. In addition, PE_PGRS1 can mitigate the activation of PERK branch in endoplasmic reticulum (ER) stress by down-regulating the expression of CHOP, Bip, p-PERK, p-eIF2α, and ATF4 . Interestingly, we found that two splicing variations of Bax/Bcl-2, Baxβ, and Bcl-2α, were differentially expressed after infection with Ms_PE_PGRS1, and may be involved in the regulation of apoptosis . Hence, this study identified that PE_PGRS1 is a novel calcium-associated protein that can decrease intracellular Ca 2+ levels and the PERK axis. And the weakening of the PERK-eIF2α-ATF4 axis reduces THP-1 macrophages apoptosis, promotes the survival of mycobacteria in macrophages.
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