C Qiu1, J Ma, M-L Wang, Q Zhang, Y-B Li. 1. Department of Neurosurgery, the Second Affiliated Hospital of Nanjing Medical University, Nanjing, China. 352430864@qq.com.
Abstract
OBJECTIVE: A lot of mammalian micro-RNAs have been identified in regulating immune system function. Here, the aim of this study was to investigate the role of microRNA-155 in promoting anti-glioma ability and its potential mechanism. MATERIALS AND METHODS: In this study, we constructed microRNA-155 knockout mouse model and glioma mouse model. Subsequently, the progression of glioma and the accumulation of CD8+ T cells were compared between WT and miR-155-/- mice. T cells were transfected with miR-155 mimics and inhibitors, and the proliferative and invasive activities were analyzed. At the same time, we evaluated Akt and Stat5 signaling transduction and the expression level of FoxO3a. Finally, the regulatory ability of FoxO3a to Akt and Stat5 signaling was determined by changing the expression level of FoxO3a in T cells. RESULTS: We found significantly increased progression of glioma in MicroRNA-155 deficiency mice with reduced accumulation of CD8+ T cells in glioma. The proliferative and invasive abilities of T cells were regulated by MicroRNA-155. Besides, microRNA-155 could induce the activation of Akt and Stat5 signaling by inhibiting its target gene FoxO3a. Furthermore, FoxO3a was a negative regulator of Akt and Stat5 signaling. CONCLUSIONS: MicroRNA-155 deficiency in CD8+ T cells inhibited anti-tumor activity by suppressing the proliferative and invasive activities of T cells. FoxO3a was a negative regulator of Akt and Stat5 signaling. Besides, microRNA-155 regulated the function of T cells by inhibiting the expression of FoxO3a. Our findings might be a new strategy for the immunotherapy of glioma.
OBJECTIVE: A lot of mammalian micro-RNAs have been identified in regulating immune system function. Here, the aim of this study was to investigate the role of microRNA-155 in promoting anti-glioma ability and its potential mechanism. MATERIALS AND METHODS: In this study, we constructed microRNA-155 knockout mouse model and gliomamouse model. Subsequently, the progression of glioma and the accumulation of CD8+ T cells were compared between WT and miR-155-/- mice. T cells were transfected with miR-155 mimics and inhibitors, and the proliferative and invasive activities were analyzed. At the same time, we evaluated Akt and Stat5 signaling transduction and the expression level of FoxO3a. Finally, the regulatory ability of FoxO3a to Akt and Stat5 signaling was determined by changing the expression level of FoxO3a in T cells. RESULTS: We found significantly increased progression of glioma in MicroRNA-155 deficiency mice with reduced accumulation of CD8+ T cells in glioma. The proliferative and invasive abilities of T cells were regulated by MicroRNA-155. Besides, microRNA-155 could induce the activation of Akt and Stat5 signaling by inhibiting its target gene FoxO3a. Furthermore, FoxO3a was a negative regulator of Akt and Stat5 signaling. CONCLUSIONS:MicroRNA-155 deficiency in CD8+ T cells inhibited anti-tumor activity by suppressing the proliferative and invasive activities of T cells. FoxO3a was a negative regulator of Akt and Stat5 signaling. Besides, microRNA-155 regulated the function of T cells by inhibiting the expression of FoxO3a. Our findings might be a new strategy for the immunotherapy of glioma.
Authors: Mohammad Taheri; Dominik A Barth; Julia Kargl; Omidvar Rezaei; Soudeh Ghafouri-Fard; Martin Pichler Journal: Front Immunol Date: 2021-11-04 Impact factor: 7.561