Medical Research Center, The Affiliated Hospital of Qingdao University, Wutaishan road 1677, Qingdao, 266000, People's Republic of China.
Qingdao Municipal Hospital, University of Health and Rehabilitation Sciences, Jiaozhou road 1, Qingdao, 266000, People's Republic of China.
Sci Rep. 2024 Nov 20;14(1):28702. doi: 10.1038/s41598-024-79008-8.
Tregs and M2-type macrophages are essential for immune surveillance. CD38 + NK cells are involved in immunoregulation by modulating cytokine secretion. This study investigated how CD38 + NKs affect Tregs and macrophages in colorectal cancer (CRC). Higher proportions of CD38 + NKs and Tregs were detected in bloods and tumor tissues of CRC patients than that in the samples from healthy controls (HCs). Compared with CD38 + NKs from HCs, the NK cells from CRC promoted the differentiation of Tregs from CD4 + T cells, and secreted increased levels of IL-10, TGF-β and TNF-α and decreased levels of IFN-γ. CD38 + NKs from CRC expressed higher levels of CD38, NF-κB and acetyl-NF-κB and lower levels of Sirt1. When CRC CD38 + NK cells were treated with anti-CD38 monoclonal antibody, the above trends were reversed. CRC CD38 + NKs with treatment of NF-κB inhibitor also showed opposite effects on cytokine secretion and CD4 + T-cell differentiation. After treatment with a Sirt1 activator, NF-κB signaling was inhibited in these CD38 + NKs, whereas treatment with a Sirt1 inhibitor activated NF-κB signaling. The supernatants of CRC CD38 + NK culture promoted M0 macrophage polarization to M2-type. We suggest that CD38 modulates cytokine secretion by NK cells through Sirt1/NF-κB signaling pathway, thereby suppressing immune surveillance in tumorigenesis.
调节性 T 细胞(Tregs)和 M2 型巨噬细胞对于免疫监视至关重要。CD38+NK 细胞通过调节细胞因子分泌参与免疫调节。本研究旨在探讨 CD38+NK 细胞如何影响结直肠癌(CRC)中的 Tregs 和巨噬细胞。CRC 患者的血液和肿瘤组织中 CD38+NK 细胞和 Tregs 的比例高于健康对照(HC)样本。与 HC 来源的 CD38+NK 细胞相比,CRC 来源的 NK 细胞促进 CD4+T 细胞分化为 Tregs,且分泌更高水平的 IL-10、TGF-β 和 TNF-α,以及更低水平的 IFN-γ。CRC 来源的 CD38+NK 细胞表达更高水平的 CD38、NF-κB 和乙酰化-NF-κB,以及更低水平的 Sirt1。当用抗 CD38 单克隆抗体处理 CRC CD38+NK 细胞时,上述趋势被逆转。用 NF-κB 抑制剂处理的 CRC CD38+NK 细胞对细胞因子分泌和 CD4+T 细胞分化也表现出相反的作用。用 Sirt1 激活剂处理后,这些 CD38+NK 细胞中的 NF-κB 信号被抑制,而用 Sirt1 抑制剂处理则激活 NF-κB 信号。CRC CD38+NK 细胞培养物的上清液促进 M0 巨噬细胞向 M2 型极化。我们认为,CD38 通过 Sirt1/NF-κB 信号通路调节 NK 细胞细胞因子分泌,从而抑制肿瘤发生过程中的免疫监视。