Department of Materials Sciences and Engineering, Stony Brook University, Stony Brook, NY 11794-2275, USA.
Biomaterials. 2011 Nov;32(31):7831-8. doi: 10.1016/j.biomaterials.2011.06.053. Epub 2011 Aug 4.
We have investigated the effects of moderate static magnetic fields (SMFs) on murine MC3T3-E1 osteoblasts, and found that they enhance proliferations and promote differentiation. The increase in proliferation rates in response to SMFs was greater in cultures grown on partially sulfonated polytstyrene (SPS, degree of sulfonation: 33%) than in cultures grown on tissue culture plastic. We have previously shown that when the degree of sulfonation exceeded a critical value (12%) [1], spontaneous fibrillogenesis occured which allowed for direct observation of the ECM fibrillar organization under the influence of external fields. We found that the ECM produced in cultures grown on the SPS in the presence of the SMFs assembled into a lattice with larger dimensions than the ECM of the cultures grown in the absence of SMFs. During the early stages of the biomineralization process (day 7), the SMF exposed cultures also templated mineral deposition more rapidly than the control cultures. The rapid response is attributed to orientation of diamagnetic ECM proteins already present in the serum, which could then initiate further cellular signaling. SMFs also influenced late stage osteoblast differentiation as measured by the increased rate of osteocalcin secretion and gene expression beginning 15 days after SFM exposure. This correlated with a large increase in mineral deposition, and in cell modulus. GIXD and EDXS analysis confirmed early deposition of crystalline hydroxyapatite. Previous studies on the effects of moderate SMF had focused on cellular gene and protein expression, but did not consider the organization of the ECM fibers. Our ability to form these fibers has allowed us explore this additional effect and highlight its significance in the initiation of the biomineralization process.
我们研究了中等静磁场(SMFs)对鼠 MC3T3-E1 成骨细胞的影响,发现它们能促进细胞增殖和分化。在部分磺化聚苯乙烯(SPS,磺化度:33%)上培养的细胞对 SMFs 的增殖反应比在组织培养塑料上培养的细胞更大。我们之前已经表明,当磺化度超过临界值(12%)[1]时,会自发发生原纤维形成,从而可以在外部场的影响下直接观察细胞外基质的纤维组织。我们发现,在 SMFs 存在下在 SPS 上培养的细胞产生的细胞外基质组装成具有比没有 SMFs 的细胞外基质更大尺寸的晶格。在生物矿化过程的早期阶段(第 7 天),暴露于 SMF 的培养物也比对照培养物更快地模板化矿物质沉积。这种快速响应归因于已经存在于血清中的抗磁性细胞外基质蛋白的取向,这可以启动进一步的细胞信号转导。SMFs 还通过增加骨钙素分泌和基因表达的速率来影响晚期成骨细胞分化,从暴露于 SFM 后 15 天开始。这与矿物质沉积和细胞模量的大幅增加相关。GIXD 和 EDXS 分析证实了早期结晶羟磷灰石的沉积。以前关于中等 SMF 影响的研究主要集中在细胞基因和蛋白质表达上,但没有考虑细胞外基质纤维的组织。我们形成这些纤维的能力使我们能够探索这种额外的效果,并强调其在生物矿化过程启动中的重要性。