Division of Tumor and Cellular Biochemistry, Department of Medical Sciences, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Laboratory of Molecular and Cellular Physiology, Graduate School of Pharmaceutical Sciences, Osaka University, Osaka, Japan.
Sci Rep. 2019 Jan 23;9(1):429. doi: 10.1038/s41598-018-36796-0.
Ecotropic viral integration site-1 (EVI1) has a critical role in normal and malignant hematopoiesis. Since we previously identified high expression of calcitonin receptor like receptor (CRLR) in acute myeloid leukemia (AML) with high EVI1 expression, we here characterized the function of CRLR in hematopoiesis. Since higher expression of CRLR and receptor activity modifying protein 1 (RAMP1) was identified in immature hematopoietic bone marrow (BM) cells, we focused on calcitonin gene-related peptide (CGRP), a specific ligand for the CRLR/RAMP1 complex. To elucidate the role of CGRP in hematopoiesis, Ramp1-deficient (Ramp1) mice were used. The steady-state hematopoiesis was almost maintained in Ramp1 mice; however, the BM repopulation capacity of Ramp1 mice was significantly decreased, and the transplanted Ramp1 BM mononuclear cells had low proliferation capacity with enhanced reactive oxygen species (ROS) production and cell apoptosis. Thus, CGRP is important for maintaining hematopoiesis during temporal exposures with proliferative stress. Moreover, continuous CGRP exposure to mice for two weeks induced a reduction in the number of BM immature hematopoietic cells along with differentiated myeloid cells. Since CGRP is known to be increased under inflammatory conditions to regulate immune responses, hematopoietic exhaustion by continuous CGRP secretion under chronic inflammatory conditions is probably one of the important mechanisms of anti-inflammatory responses.
嗜病毒整合位点 1(EVI1)在正常和恶性造血中具有关键作用。由于我们之前在高表达 EVI1 的急性髓系白血病(AML)中发现了降钙素受体样受体(CRLR)的高表达,因此我们在此表征了 CRLR 在造血中的功能。由于在不成熟的造血骨髓(BM)细胞中鉴定出更高表达的 CRLR 和受体活性修饰蛋白 1(RAMP1),我们专注于降钙素基因相关肽(CGRP),它是 CRLR/RAMP1 复合物的特异性配体。为了阐明 CGRP 在造血中的作用,使用了缺乏 RAMP1(Ramp1)的小鼠。Ramp1 小鼠中的稳态造血几乎得到维持;然而,Ramp1 小鼠的 BM 重编程能力显著降低,并且移植的 Ramp1 BM 单核细胞增殖能力降低,同时产生更多的活性氧(ROS)并发生细胞凋亡。因此,CGRP 对于在增殖应激的短暂暴露期间维持造血很重要。此外,连续两周向小鼠暴露于 CGRP 会导致 BM 不成熟造血细胞数量减少,同时分化的髓样细胞也减少。由于已知 CGRP 在炎症条件下增加以调节免疫反应,因此在慢性炎症条件下持续 CGRP 分泌引起的造血衰竭可能是抗炎反应的重要机制之一。