Norton L A, Rovetti L A
Department of Orthodontics, University of Connecticut Health Center, School of Dental Medicine, Farmington 06032.
J Orthop Res. 1988;6(4):559-66. doi: 10.1002/jor.1100060413.
We tested the hypothesis that electric perturbation influences 45Ca incorporation in extracellular matrix (ECM) of cartilage in vitro. Hypertrophic chondroblasts of tibial epiphyses (HC), sternum (SC), and skin fibroblasts (F) were cultured from chick embryos. HC, SC, and F cells were micromass seeded three times per week and maintained at 37.5 degrees C with 5% CO2 for two weeks. Cultures were randomly designated control (C) or exposed (E) to a pulsed electromagnetic field (PEMF). A time course experiment of calcium incorporation for all cultured groups showed that 24 h of exposure produced the largest biological response in chondroblasts. Calcium incorporation required supplemental phosphate. Autoradiography data indicated that the calcium incorporation into macromolecules largely occurred in the ECM. 45Ca steady-state perturbation was enhanced by Streptomyces hyaluronidase (SH) but not by testicular hyaluronidase (TH). 45Ca incorporation experiments tested the effects of phosphate, SH, TH, and PEMF alone and in various combinations on these cultures. Only PEMF or SH plus PEMF with phosphate enhanced 45Ca incorporation. Other experiments examined the effect of rotenone or freeze-thawing on cells exposed to PEMF. PEMF plus freeze-thaw enhanced calcium incorporation in HC only. PEMF appeared to cause disruption of the ECM, enhancing the probability of matrix calcification.
电扰动在体外影响软骨细胞外基质(ECM)中45Ca的掺入。从鸡胚中培养出胫骨骨骺的肥大软骨细胞(HC)、胸骨软骨细胞(SC)和皮肤成纤维细胞(F)。HC、SC和F细胞每周进行三次微团接种,并在37.5摄氏度、5%二氧化碳条件下培养两周。将培养物随机分为对照组(C)或暴露于脉冲电磁场(PEMF)的暴露组(E)。对所有培养组进行的钙掺入时间进程实验表明,暴露24小时在软骨细胞中产生了最大的生物学反应。钙掺入需要补充磷酸盐。放射自显影数据表明,钙掺入大分子主要发生在ECM中。透明质酸酶(SH)可增强45Ca稳态扰动,但睾丸透明质酸酶(TH)则无此作用。45Ca掺入实验测试了磷酸盐、SH、TH和PEMF单独及各种组合对这些培养物的影响。只有PEMF或SH加PEMF与磷酸盐一起可增强45Ca掺入。其他实验研究了鱼藤酮或冻融对暴露于PEMF的细胞的影响。PEMF加冻融仅增强了HC中的钙掺入。PEMF似乎导致了ECM的破坏,增加了基质钙化的可能性。