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在小鼠中删除假定的巨噬细胞迁移抑制因子(MIF)受体CD74会增强破骨细胞生成并降低骨量。

Deletion of CD74, a putative MIF receptor, in mice enhances osteoclastogenesis and decreases bone mass.

作者信息

Mun Se Hwan, Won Hee Yeon, Hernandez Paula, Aguila Hector Leonardo, Lee Sun-Kyeong

机构信息

UCONN Center on Aging, University of Connecticut Health Center, Farmington, CT 06030-1835, USA.

出版信息

J Bone Miner Res. 2013 Apr;28(4):948-59. doi: 10.1002/jbmr.1787.

Abstract

CD74 is a type II transmembrane protein that can act as a receptor for macrophage migration inhibitory factor (MIF) and plays a role in MIF-regulated responses. We reported that MIF inhibited osteoclast formation and MIF knockout (KO) mice had decreased bone mass. We therefore examined if CD74 was involved in the ability of MIF to alter osteoclastogenesis in cultured bone marrow (BM) from wild-type (WT) and CD74-deficient (KO) male mice. We also measured the bone phenotype of CD74 KO male mice. Bone mass in the femur of 8-week-old mice was measured by micro-computed tomography and histomorphometry. Bone marrow cells from CD74 KO mice formed 15% more osteoclast-like cells (OCLs) with macrophage colony-stimulating factor (M-CSF) and receptor activator of NF-κB ligand (RANKL) (both at 30 ng/mL) compared to WT. Addition of MIF to WT cultures inhibited OCL formation by 16% but had no effect on CD74KO cultures. The number of colony forming unit granulocyte-macrophage (CFU-GM) in the bone marrow of CD74 KO mice was 26% greater than in WT controls. Trabecular bone volume (TBV) in the femurs of CD74 KO male mice was decreased by 26% compared to WT. In addition, cortical area and thickness were decreased by 14% and 11%, respectively. Histomorphometric analysis demonstrated that tartrate-resistant acid phosphatase (TRAP)(+) osteoclast number and area were significantly increased in CD74 KO by 35% and 43%, respectively compared to WT. Finally, we examined the effect of MIF on RANKL-induced-signaling pathways in bone marrow macrophage (BMM) cultures. MIF treatment decreased RANKL-induced nuclear factor of activated T cells, cytoplasmic 1 (NFATc1) and c-Fos protein in BMM cultures by 70% and 41%, respectively. Our data demonstrate that CD74 is required for MIF to affect in vitro osteoclastogenesis. Further, the bone phenotype of CD74 KO mice is similar to that of MIF KO mice. MIF treatment of WT cultures suppressed RANKL-induced activator protein 1 (AP-1) expression, which resulted in decreased osteoclast differentiation in vitro. We propose that CD74 plays a critical role in the MIF inhibition of osteoclastogenesis.

摘要

CD74是一种II型跨膜蛋白,可作为巨噬细胞迁移抑制因子(MIF)的受体,并在MIF调节的反应中发挥作用。我们报道过MIF抑制破骨细胞形成,且MIF基因敲除(KO)小鼠的骨量减少。因此,我们研究了CD74是否参与MIF改变野生型(WT)和CD74缺陷型(KO)雄性小鼠培养骨髓(BM)中破骨细胞生成的能力。我们还测量了CD74 KO雄性小鼠的骨表型。通过显微计算机断层扫描和组织形态计量学测量8周龄小鼠股骨的骨量。与WT相比,CD74 KO小鼠的骨髓细胞在巨噬细胞集落刺激因子(M-CSF)和核因子κB受体活化因子配体(RANKL)(均为30 ng/mL)作用下形成的破骨细胞样细胞(OCL)多15%。向WT培养物中添加MIF可使OCL形成减少16%,但对CD74 KO培养物无影响。CD74 KO小鼠骨髓中的粒细胞-巨噬细胞集落形成单位(CFU-GM)数量比WT对照多26%。与WT相比,CD74 KO雄性小鼠股骨的小梁骨体积(TBV)减少了26%。此外,皮质面积和厚度分别减少了14%和11%。组织形态计量学分析表明,与WT相比,CD74 KO中抗酒石酸酸性磷酸酶(TRAP)(+)破骨细胞数量和面积分别显著增加35%和43%。最后,我们研究了MIF对骨髓巨噬细胞(BMM)培养物中RANKL诱导的信号通路的影响。MIF处理使BMM培养物中RANKL诱导的活化T细胞核因子细胞质1(NFATc1)和c-Fos蛋白分别减少70%和41%。我们的数据表明,MIF影响体外破骨细胞生成需要CD74。此外,CD74 KO小鼠的骨表型与MIF KO小鼠相似。WT培养物经MIF处理可抑制RANKL诱导的活化蛋白1(AP-1)表达,从而导致体外破骨细胞分化减少。我们认为CD74在MIF抑制破骨细胞生成中起关键作用。

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