| Autor: |
Li, Rongqing, Sun, Na, Chen, Xin, Li, Xueqin, Zhao, Jie, Cheng, Wanpeng, Hua, Hui, Fukatsu, Masahiko, Mori, Hirotaka, Takahashi, Hiroshi, Ohkawara, Hiroshi, Fukami, Miwa, Okamoto, Masatoshi, Hamazaki, Yoichi, Zheng, Kuiyang, Yang, Jing, Ikezoe, Takayuki |
| Předmět: |
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| Zdroj: |
Frontiers in Immunology; 2/8/2021, Vol. 11, pN.PAG-N.PAG, 12p |
| Abstrakt: |
A substitution mutation of valine to phenylalanine at codon encoding position 617 of the Janus kinase 2 (JAK2) gene (JAK2V617F) has been detected in myeloid cells of some individuals with higher levels of proinflammatory cytokine production such as interleukin (IL)-6. However, the mechanisms by which JAK2V617F mutation mediating those cytokines remain unclear. We, therefore, established JAK2V617F -expressing murine macrophages (JAK2V617F macrophages) and found that the levels of p-STAT3 were markedly elevated in JAK2V617F macrophages in association with an increase in IL-6 production. However, inhibition of STAT3 by C188-9 significantly decreased the production of IL-6. Furthermore, the JAK2V617F mutation endowed macrophages with an elevated glycolytic phenotype in parallel with aberrant expression of PKM1. Interestingly, silencing of PKM1 inactivated STAT3 in parallel with reduced IL-6 production. In contrast, ectopic expression of PKM1 elevated IL-6 production via STAT3 activation. Importantly, the JAK2V617F mutation contributed to PKM1 protein stabilization via blockade of lysosomal-dependent degradation via chaperone-mediated autophagy (CMA), indicating that the JAK2V617F mutation could protect PKM1 from CMA-mediated degradation, leading to activation of STAT3 and promoting IL-6 production. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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