Vicioso Yorleny, Wong Derek P, Roy Nand K, Das Nayanika, Zhang Keman, Ramakrishnan Parameswaran, Parameswaran Reshmi
Department of Pathology, Case Western Reserve University, Cleveland, OH, United States.
Division of Hematology/Oncology, Department of Medicine, Case Western Reserve University, Cleveland, OH, United States.
Front Immunol. 2021 Apr 29;12:652786. doi: 10.3389/fimmu.2021.652786. eCollection 2021.
Natural Killer (NK) cells are cytotoxic lymphocytes critical to the innate immune system. We found that germline deficiency of NF-κB c-Rel results in a marked decrease in cytotoxic function of NK cells, both and , with no significant differences in the stages of NK cell development. We found that c-Rel binds to the promoters of perforin and granzyme B, two key proteins required for NK cytotoxicity, and controls their expression. We generated a NK cell specific c-Rel conditional knockout to study NK cell intrinsic role of c- Rel and found that both global and conditional c-Rel deficiency leads to decreased perforin and granzyme B expression and thereby cytotoxic function. We also confirmed the role of c-Rel in perforin and granzyme B expression in human NK cells. c-Rel reconstitution rescued perforin and granzyme B expressions in c-Rel deficient NK cells and restored their cytotoxic function. Our results show a previously unknown role of c-Rel in transcriptional regulation of perforin and granzyme B expressions and control of NK cell cytotoxic function.
自然杀伤(NK)细胞是先天性免疫系统中至关重要的细胞毒性淋巴细胞。我们发现,NF-κB c-Rel的种系缺陷导致NK细胞的细胞毒性功能显著下降,无论是在[此处可能缺失部分内容]还是[此处可能缺失部分内容],而NK细胞发育阶段无显著差异。我们发现,c-Rel与穿孔素和颗粒酶B的启动子结合,这两种是NK细胞毒性所需的关键蛋白质,并控制它们的表达。我们构建了NK细胞特异性的c-Rel条件性敲除小鼠,以研究c-Rel在NK细胞中的内在作用,发现全身性和条件性c-Rel缺陷均导致穿孔素和颗粒酶B表达降低,从而导致细胞毒性功能下降。我们还证实了c-Rel在人NK细胞中对穿孔素和颗粒酶B表达的作用。c-Rel的重建挽救了c-Rel缺陷型NK细胞中穿孔素和颗粒酶B的表达,并恢复了它们的细胞毒性功能。我们的结果显示了c-Rel在穿孔素和颗粒酶B表达的转录调控以及NK细胞毒性功能控制方面以前未知的作用。