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光生物调节对成骨细胞-破骨细胞共培养体系中骨重塑的影响。

Effects of photobiomodulation on bone remodeling in an osteoblast-osteoclast co-culture system.

机构信息

Department of Oral and Maxillofacial Surgery, Dental Research Institute, and Dental and Life Science Institute, School of Dentistry, Pusan National University, Yangsan, 50611, Korea.

Department of Oral Physiology, Periodontal Diseases Signaling Network Research Center, and Dental and Life Science Institute, School of Dentistry, Pusan National University, Yangsan, 50611, Korea.

出版信息

Lasers Med Sci. 2022 Mar;37(2):1049-1059. doi: 10.1007/s10103-021-03352-8. Epub 2021 Jun 17.

Abstract

The general bone anabolic effect of photobiomodulation (PBM) is largely accepted. As a result, PBM therapy is expected to be beneficial in the medical fields of dentistry and bone healing. However, most of the previous in vitro studies on PBM and bone metabolism were performed with single-cell cultures of osteoclast-lineage cells or osteoblast-lineage cells. In the present study, the bone-modulating effects of PBM were evaluated in an in vitro osteoblast/osteoclast co-culture system. Mouse bone marrow-derived macrophages (BMMs) and mouse calvarial pre-osteoblasts cells were purified and used as precursor cells for osteoclasts and osteoblasts, respectively. The PBM effects on single-cell culture of osteoclasts or osteoblasts as well as co-culture were examined by 1.2 J/cm low-level Ga-Al-As laser (λ  = 808 ± 3 nm, 80 mW, and 80 mA; spot size, 1cm; NDLux, Seoul, Korea) irradiation for 30 s at daily intervals throughout culture period. At the end of culture, the osteoclast differentiation and osteoblast differentiation were assessed by TRAP staining and ALP staining, respectively. The expressions of osteoclastogenic cytokines were evaluated by RT-PCR and Western blot analyses. Under the single-cell culture condition, PBM enhanced osteoblast differentiation but had minor effects on osteoclast differentiation. However, in the co-culture condition, its osteoblastogenic effect was maintained, and osteoclast differentiation was substantially reduced. Subsequent RT-PCR analyses and western blot results revealed marked reduction in receptor activator of NF-κB ligand (RANKL) expression and elevation in osteoprotegerin (OPG) expression by PBM in co-cultured cells. More importantly, these alterations in RANKL/OPG levels were not observed under the single-cell culture conditions. Our results highlight the different effects of PBM on bone cells based on culture conditions. Further, our findings suggest the indirect anti-osteoclastogenic effect of PBM, which is accompanied by a decrease in RANKL expression and an increase in OPG expression.

摘要

光生物调节(PBM)的普遍骨 anabolic 效应已被广泛接受。因此,PBM 疗法有望在牙科和骨愈合等医学领域发挥作用。然而,之前大多数关于 PBM 和骨代谢的体外研究都是在破骨细胞系细胞或成骨细胞系细胞的单细胞培养中进行的。在本研究中,我们在体外成骨细胞/破骨细胞共培养系统中评估了 PBM 的骨调节作用。从小鼠骨髓来源的巨噬细胞(BMM)和小鼠颅骨前成骨细胞中分离纯化出破骨细胞和成骨细胞的前体细胞,并分别用作破骨细胞和成骨细胞的前体细胞。通过每日间隔对细胞进行 1.2 J/cm 低水平 Ga-Al-As 激光(λ  = 808 ± 3 nm、80 mW 和 80 mA;光斑尺寸 1cm;NDLux,首尔,韩国)照射 30 s,在整个培养过程中进行照射。在培养结束时,通过 TRAP 染色和 ALP 染色分别评估破骨细胞分化和成骨细胞分化。通过 RT-PCR 和 Western blot 分析评估破骨细胞生成细胞因子的表达。在单细胞培养条件下,PBM 增强了成骨细胞分化,但对破骨细胞分化的影响较小。然而,在共培养条件下,其成骨细胞作用得以维持,破骨细胞分化则显著减少。随后的 RT-PCR 分析和 Western blot 结果表明,PBM 可显著降低共培养细胞中核因子 κB 受体激活剂配体(RANKL)的表达,并升高护骨素(OPG)的表达。更重要的是,在单细胞培养条件下,未观察到 RANKL/OPG 水平的这些变化。我们的研究结果强调了基于培养条件的 PBM 对骨细胞的不同作用。此外,我们的研究结果表明,PBM 具有间接的抗破骨细胞生成作用,其机制是降低 RANKL 表达和增加 OPG 表达。

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