Wang Xiaomin, Li Minghao, Gao Yanan, Gao Juan, Yang Wanzhu, Liang Haoyue, Ji Qing, Li Yanxin, Liu Hanzhi, Huang Jian, Cheng Tao, Yuan Weiping
State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Center for Stem Cell Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin 300020, China.
Department of Pathology and Laboratory Medicine, School of Medicine, Temple University, Philadelphia, PA 19140, USA.
Exp Cell Res. 2016 Jun 10;344(2):219-28. doi: 10.1016/j.yexcr.2016.04.017. Epub 2016 May 7.
Ras homolog enriched in brain (Rheb1) is a small GTPase and is known to be a direct activator of mTORC1. Dysregulation of Rheb1 has been shown to impair the cellular-energetic state and cell homeostasis. However, the role of Rheb1 in monocytes/macrophages differentiation and maturation is not clear. Here, we investigate the role of Rheb1 in mouse myelopoiesis using a Rheb1 conditional deletion murine model. We found that the absolute number of macrophages decreased in the bone marrow (BM) of Rheb1-deficient mice. Loss of Rheb1 inhibited the monocyte-to-macrophage differentiation process. Additionally, Rheb1 deletion reduced phagocytosis ability of macrophages by inhibiting the mTORC1 signaling pathway. Furthermore, 3BDO (an activator of mTORC1) rescued the phagocytosis ability of Rheb1-deficient macrophages. Thus, Rheb1 is critical for macrophage production and phagocytosis and executes these activities possibly via mTORC1-dependent pathway.
富含脑的Ras同源物(Rheb1)是一种小GTP酶,已知是mTORC1的直接激活剂。已表明Rheb1的失调会损害细胞能量状态和细胞稳态。然而,Rheb1在单核细胞/巨噬细胞分化和成熟中的作用尚不清楚。在此,我们使用Rheb1条件性缺失小鼠模型研究Rheb1在小鼠骨髓生成中的作用。我们发现Rheb1缺陷小鼠骨髓(BM)中巨噬细胞的绝对数量减少。Rheb1的缺失抑制了单核细胞向巨噬细胞的分化过程。此外,Rheb1的缺失通过抑制mTORC1信号通路降低了巨噬细胞的吞噬能力。此外,3BDO(mTORC1的激活剂)挽救了Rheb1缺陷巨噬细胞的吞噬能力。因此,Rheb1对巨噬细胞的产生和吞噬至关重要,并可能通过mTORC1依赖性途径执行这些活动。