Cell volume controlled by LRRC8A-formed volume-regulated anion channels fine-tunes T cell activation and function
Year: 2023
Type: article
Abstract: Biosynthesis drives the cell volume increase during T cell activation. However, the contribution of cell volume regulation in TCR signaling during T lymphoblast formation and its underlying mechanisms remain unclear. Here we show that cell volume regulation is required for optimal T cell activation. Inhibition of VRACs (volume-regulated anion channels) and deletion of leucine-rich repeat-containing protein 8A (LRRC8A) channel components impair T cell activation and function, particularly under weak TCR stimulation. Additionally, LRRC8A has distinct influences on mRNA transcriptional profiles, indicating the prominent effects of cell volume regulation for T cell functions. Moreover, cell volume regulation via LRRC8A controls T cell-mediated antiviral immunity and shapes the TCR repertoire in the thymus. Mechanistically, LRRC8A governs stringent cell volume increase via regulated volume decrease (RVD) during T cell blast formation to keep the TCR signaling molecules at an adequate density. Together, our results show a further layer of T cell activation regulation that LRRC8A functions as a cell volume controlling "valve" to facilitate T cell activation.
Source: Nature Communications
Authors: Yuman Wang, Zaiqiao Sun, Jieming Ping, Jianlong Tang, Boxiao He, Teding Chang, Qian Zhou, Shijie Yuan, Zhaohui Tang, Xin Li, Yan Lu, Ran He, Ximiao He, Zheng Liu, Lei Yin, Ning Wu
Institutions: Huazhong University of Science and Technology, Wuhan University, Renmin Hospital of Wuhan University, State Key Laboratory of Virology, Tongji Hospital, Guangdong Academy of Medical Sciences, Guangdong Provincial People's Hospital, Third Affiliated Hospital of Sun Yat-sen University, Anhui Medical University, First Affiliated Hospital of Anhui Medical University
Language: English
Topic: T-cell and B-cell Immunology
Subfield: Immunology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $6,290
Awards: G5399820550, G838428866
OpenAlex ID: W4388348232
