NAD+激酶
CD38
烟酰胺腺嘌呤二核苷酸
细胞内
细胞生物学
信号转导
免疫系统
生物化学
生物
细胞
化学
酶
干细胞
川地34
作者
Anwesha Kar,Shikhar Mehrotra,Shilpak Chatterjee
出处
期刊:Cells
[Multidisciplinary Digital Publishing Institute]
日期:2020-07-17
卷期号:9 (7): 1716-1716
被引量:38
摘要
Activation and subsequent differentiation of T cells following antigenic stimulation are triggered by highly coordinated signaling events that lead to instilling cells with a discrete metabolic and transcriptional feature. Compelling studies indicate that intracellular nicotinamide adenine dinucleotide (NAD+) levels have profound influence on diverse signaling and metabolic pathways of T cells, and hence dictate their functional fate. CD38, a major mammalian NAD+ glycohydrolase (NADase), expresses on T cells following activation and appears to be an essential modulator of intracellular NAD+ levels. The enzymatic activity of CD38 in the process of generating the second messenger cADPR utilizes intracellular NAD+, and thus limits its availability to different NAD+ consuming enzymes (PARP, ART, and sirtuins) inside the cells. The present review discusses how the CD38-NAD+ axis affects T cell activation and differentiation through interfering with their signaling and metabolic processes. We also describe the pivotal role of the CD38-NAD+ axis in influencing the chromatin remodeling and rewiring T cell response. Overall, this review emphasizes the crucial contribution of the CD38-NAD+ axis in altering T cell response in various pathophysiological conditions.
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