Max Planck Institute of Colloids and Interfaces, Department of Biomaterials, 14476 Potsdam, Germany.
Max Planck Institute of Colloids and Interfaces, Department of Biomaterials, 14476 Potsdam, Germany.
Bone. 2024 Dec;189:117236. doi: 10.1016/j.bone.2024.117236. Epub 2024 Aug 14.
Osteocytes are mechanosensitive, bone-embedded cells which are connected via dendrites in a lacuno-canalicular network and regulate bone resorption and formation balance. Alterations in osteocyte lacunar volume, shape and density have been identified in conditions of aging, osteoporosis and osteolytic bone metastasis, indicating patterns of impaired bone remodeling, osteolysis and disease progression. Osteolytic bone disease is a hallmark of the hematologic malignancy multiple myeloma (MM), in which monoclonal plasma cells in the bone marrow disrupt the bone homeostasis and induce excessive resorption at local and distant sites. Qualitative and quantitative changes in the 3D osteocyte lacunar morphometry have not yet been evaluated in MM, nor in the precursor conditions monoclonal gammopathy of undetermined significance (MGUS) and smoldering multiple myeloma (SMM). In this study, we characterized the osteocyte lacunar morphology in trabecular bone of the iliac crest at the ultrastructural level using high resolution microCT in human bone biopsy samples of three MGUS, two SMM and six newly diagnosed MM. In MGUS, SMM and MM we found a trend for lower lacunar density and a shift towards larger lacunae with disease progression (higher 50 % cutoff of the lacunar volume cumulative distribution) in the small osteocyte lacunae 20-900 μm range compared to control samples. In the larger lacunae 900-3000 μm range, we detected significantly higher lacunar density and microporosity in the MM group compared to the MGUS/SMM group. Regarding the shape distribution, the MGUS/SMM group showed a trend for flatter, more elongated and anisotropic osteocyte lacunae compared to the control group. Altogether, our findings suggest that osteocytes in human MM bone disease undergo changes in their lacunae density, volume and shape, which could be an indicator for osteolysis and disease progression. Future studies are needed to understand whether alterations of the lacunae architecture affect the mechanoresponsiveness of osteocytes, and ultimately bone adaptation and fracture resistance in MM and its precursors conditions.
成骨细胞是机械敏感的,嵌入在骨中的细胞,通过在腔隙 - 小管网络中的树突连接,并调节骨吸收和形成平衡。在衰老、骨质疏松症和溶骨性骨转移等情况下,已经发现成骨细胞腔隙体积、形状和密度发生了改变,表明骨重塑、溶骨和疾病进展受损的模式。溶骨性骨疾病是血液恶性肿瘤多发性骨髓瘤(MM)的标志,骨髓中的单克隆浆细胞破坏骨内稳态并在局部和远处部位诱导过度吸收。在 MM 中,尚未评估 3D 成骨细胞腔隙形态计量学的定性和定量变化,也未在其前体单克隆丙种球蛋白病(MGUS)和冒烟型多发性骨髓瘤(SMM)中评估。在这项研究中,我们使用高分辨率微 CT 在人类骨活检样本中对髂嵴小梁骨中的成骨细胞腔隙形态进行了超微结构水平的特征描述,这些样本包括 3 例 MGUS、2 例 SMM 和 6 例新诊断的 MM。在 MGUS、SMM 和 MM 中,我们发现随着疾病进展(较小的成骨细胞腔隙 20-900 μm 范围内的腔隙体积累积分布的 50%截点更高),腔隙密度呈下降趋势,并且腔隙向更大的腔隙转移。在较大的腔隙 900-3000 μm 范围内,我们发现 MM 组的腔隙密度和微孔率明显高于 MGUS/SMM 组。关于形状分布,MGUS/SMM 组的成骨细胞腔隙比对照组更平坦、更长和各向异性。总的来说,我们的研究结果表明,人类 MM 骨疾病中的成骨细胞在其腔隙密度、体积和形状方面发生了变化,这可能是溶骨和疾病进展的指标。未来的研究需要了解腔隙结构的改变是否会影响成骨细胞的机械响应性,以及最终影响 MM 及其前体条件下的骨适应和抗骨折能力。