微泡
细胞生物学
ESCRT公司
外体
生物
信号转导
MAPK/ERK通路
PI3K/AKT/mTOR通路
基因
细胞内
内体
小RNA
生物化学
作者
Arpana Singh,Kaushik Das,Sampali Banerjee,Prosenjit Sen
出处
期刊:Immunology
[Wiley]
日期:2022-08-06
卷期号:168 (1): 63-82
摘要
Exosomes are extracellular vesicles released by all cell types; perform several important functions such as cell-to-cell communication, growth, differentiation and so on. Exosomes elicit several signalling mechanisms as they carry information in the form of DNA, RNA or protein docked on them. We show that exosomes released from Mycobacterium tuberculosis (Mtb)-infected macrophages not only induce differentiation of naïve monocytes but also generate functionally active macrophages via MAPK-dependent signalling mechanism through MK-2 and NF-κβ activation which is completely different from the differentiation induced by exosomes from uninfected macrophages. Further, we elucidate unequivocally the signalling mechanism behind the enhanced release of exosome generation from infected macrophages driven by AKT phosphorylation involving Rab7a and Rab11a. Genes of both ESCRT-dependent and -independent pathways are found to be involved in enhanced exosomes release and are modulated by AKT. However, interestingly, the genes of the ESCRT-independent pathway are dependent on NF-κβ activation while the genes of the dependent pathway are not, suggesting two parallel signalling cascades operating in tandem.
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