Institute of Molecular Pharmacology, University Hospital RWTH Aachen, Pauwelsstr. 30, 52074, Aachen, Germany.
Institute of Anatomy and Cell Biology, University Hospital RWTH Aachen, Aachen, Germany.
Cell Commun Signal. 2024 Jun 11;22(1):322. doi: 10.1186/s12964-024-01690-y.
Bone resorption is driven through osteoclast differentiation by macrophage colony-stimulating factor (M-CSF) and receptor activator of nuclear factor kappa-Β ligand (RANKL). We noted that a disintegrin and metalloproteinase (ADAM) 10 and ADAM17 are downregulated at the expression level during osteoclast differentiation of the murine monocytic cell line RAW264.7 in response to RANKL. Both proteinases are well known to shed a variety of single-pass transmembrane molecules from the cell surface. We further showed that inhibitors of ADAM10 or ADAM17 promote osteoclastic differentiation and furthermore enhance the surface expression of receptors for RANKL and M-CSF on RAW264.7 cells. Using murine bone marrow-derived monocytic cells (BMDMCs), we demonstrated that a genetic deficiency of ADAM17 or its required regulator iRhom2 leads to increased osteoclast development in response to M-CSF and RANKL stimulation. Moreover, ADAM17-deficient osteoclast precursor cells express increased levels of the receptors for RANKL and M-CSF. Thus, ADAM17 negatively regulates osteoclast differentiation, most likely through shedding of these receptors. To assess the time-dependent contribution of ADAM10, we blocked this proteinase by adding a specific inhibitor on day 0 of BMDMC stimulation with M-CSF or on day 7 of subsequent stimulation with RANKL. Only ADAM10 inhibition beginning on day 7 increased the size of developing osteoclasts indicating that ADAM10 suppresses osteoclast differentiation at a later stage. Finally, we could confirm our findings in human peripheral blood mononuclear cells (PBMCs). Thus, downregulation of either ADAM10 or ADAM17 during osteoclast differentiation may represent a novel regulatory mechanism to enhance their differentiation process. Enhanced bone resorption is a critical issue in osteoporosis and is driven through osteoclast differentiation by specific osteogenic mediators. The present study demonstrated that the metalloproteinases ADAM17 and ADAM10 critically suppress osteoclast development. This was observed for a murine cell line, for isolated murine bone marrow cells and for human blood cells by either preferential inhibition of the proteinases or by gene knockout. As a possible mechanism, we studied the surface expression of critical receptors for osteogenic mediators on developing osteoclasts. Our findings revealed that the suppressive effects of ADAM17 and ADAM10 on osteoclastogenesis can be explained in part by the proteolytic cleavage of surface receptors by ADAM10 and ADAM17, which reduces the sensitivity of these cells to osteogenic mediators. We also observed that osteoclast differentiation was associated with the downregulation of ADAM10 and ADAM17, which reduced their suppressive effects. We therefore propose that this downregulation serves as a feedback loop for enhancing osteoclast development.
破骨细胞的分化是由巨噬细胞集落刺激因子 (M-CSF) 和核因子 κB 配体受体激活剂 (RANKL) 驱动的。我们注意到,在对 RANKL 的反应中,鼠单核细胞系 RAW264.7 的破骨细胞分化过程中,一种解整合素和金属蛋白酶 (ADAM) 10 和 ADAM17 的表达水平下调。这两种蛋白酶都非常著名,可以从细胞表面脱落各种单次跨膜分子。我们进一步表明,ADAM10 或 ADAM17 的抑制剂促进破骨细胞分化,并进一步增强 RAW264.7 细胞表面 RANKL 和 M-CSF 受体的表达。使用鼠骨髓来源的单核细胞 (BMDMCs),我们证明 ADAM17 或其必需的调节剂 iRhom2 的遗传缺陷导致对 M-CSF 和 RANKL 刺激的破骨细胞发育增加。此外,ADAM17 缺陷的破骨细胞前体细胞表达增加的 RANKL 和 M-CSF 受体。因此,ADAM17 通过脱落这些受体负调节破骨细胞分化。为了评估 ADAM10 的时间依赖性贡献,我们在 BMDMC 用 M-CSF 刺激的第 0 天或随后用 RANKL 刺激的第 7 天添加特定抑制剂来阻断这种蛋白酶。仅在第 7 天开始抑制 ADAM10 增加了正在发育的破骨细胞的大小,表明 ADAM10 在后期抑制破骨细胞分化。最后,我们可以在人外周血单核细胞 (PBMCs) 中证实我们的发现。因此,在破骨细胞分化过程中 ADAM10 或 ADAM17 的下调可能代表一种增强其分化过程的新型调节机制。增强的骨吸收是骨质疏松症的一个关键问题,是通过特定的成骨介质驱动破骨细胞分化的。本研究表明,金属蛋白酶 ADAM17 和 ADAM10 可显著抑制破骨细胞的发育。通过优先抑制蛋白酶或基因敲除,在鼠细胞系、分离的鼠骨髓细胞和人血细胞中均观察到这种情况。作为一种可能的机制,我们研究了正在发育的破骨细胞上关键成骨介质受体的表面表达。我们的发现表明,ADAM17 和 ADAM10 对破骨细胞生成的抑制作用部分可以通过 ADAM10 和 ADAM17 对表面受体的蛋白水解切割来解释,这降低了这些细胞对成骨介质的敏感性。我们还观察到破骨细胞分化与 ADAM10 和 ADAM17 的下调有关,这降低了它们的抑制作用。因此,我们提出这种下调可作为增强破骨细胞发育的反馈回路。
Cell Commun Signal. 2024-6-11
Cochrane Database Syst Rev. 2022-5-20
J Biol Chem. 2024-7
Psychopharmacol Bull. 2024-7-8
Cochrane Database Syst Rev. 2020-12-3
Cochrane Database Syst Rev. 2021-4-19
Cancers (Basel). 2025-5-19
Front Public Health. 2025-3-27
Cell Mol Life Sci. 2021-6
Front Cardiovasc Med. 2020-12-1
Int J Mol Sci. 2020-11-19
Int J Mol Sci. 2020-8-19
Biochim Biophys Acta Mol Cell Res. 2019-7-19