Porcine TLR8 signaling and its anti-infection function are disturbed by immune checkpoint receptor TIM-3 via inhibition of P13K-AKT pathway

蛋白激酶B 先天免疫系统 信号转导 免疫系统 下调和上调 PI3K/AKT/mTOR通路 磷酸化 受体 细胞生物学 生物 免疫学 生物化学 基因
作者
Wangli Zheng,Da Ao,Qi Cao,Anjing Liu,Mengjia Lv,Ziyan Sun,Huiling Zhang,Wanglong Zheng,Nanhua Chen,Jianzhong Zhu
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:269: 132018-132018
标识
DOI:10.1016/j.ijbiomac.2024.132018
摘要

Toll-like receptor 8 (TLR8), an important innate immune receptor recognizing single stranded RNA and the antiviral imidazoquinoline compounds, can activate intracellular signaling pathway and produce an inflammatory response to kill and eliminate pathogens. However, the molecular regulation mechanisms of TLR8 signaling and its anti-infection activity are not fully elucidated. Our previous transcriptome analysis of porcine TLR8 (pTLR8) signaling suggested the immune checkpoint receptor TIM-3 as the potential regulator for pTLR8. Here we investigated TIM-3 in the regulation of pTLR8 signaling and its anti-infection activity. Our results showed that porcine TIM-3 is upregulated by pTLR8 signaling and TIM-3 inhibits pTLR8 signaling activity in a negative feedback way. Accordingly, TIM-3 disturbs pTLR8 mediated anti-bacterial and anti-viral activity. Mechanistically, TIM-3 suppresses PI3K-AKT pathway by inhibiting the TLR8-PI3K p85 interaction and subsequent AKT phosphorylation which is essential for TLR8 signaling and anti-infection activity. Therefore, our study reveals new insights into innate immune TLR8 signaling and its anti-infection function.
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