Submandibular saliva from male rats modulates osteogenic differentiation of bone marrow progenitor cells In Vitro

IF 2.3 4区 医学 Q2 DENTISTRY, ORAL SURGERY & MEDICINE
Archives of oral biology Pub Date : 2026-02-01 Epub Date: 2025-12-15 DOI:10.1016/j.archoralbio.2025.106484
Gastón R. Troncoso , María V. Gangoiti , Javier Fernández-Solari , Claudia E. Mohn , María S. Molinuevo
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Abstract

Objective

To investigate the effect of submandibular saliva from male rats on the proliferation and osteoblastic differentiation of bone marrow progenitor cells.

Design

Saliva was collected and pooled from adult male rats, and the total protein content was measured. Bone marrow progenitor cells (BMPC) from adult male rats were incubated with varying concentrations of salivary protein (ranging from 0 to 30 µg/mL) to assess cell proliferation. Osteoblastic differentiation was evaluated by measuring alkaline phosphatase activity, collagen type 1 production, mineral nodule formation, and molecular markers of differentiation after 7, 15, or 21 days of saliva exposure in a differentiating culture medium. The pro-inflammatory effects of saliva on BMPC were assessed by measuring tumor necrosis factor-alpha, interleukin 1 beta, prostaglandin E2, and matrix metalloproteinases 2 and 9.

Results

Low saliva concentration stimulated BMPC, promoting a pro-secretory and proliferative state. In contrast, higher concentration inhibited both processes under basal conditions. Furthermore, in osteogenic medium, saliva decreased alkaline phosphatase activity, collagen-1 production, and matrix mineralization in BMPC, demonstrating a dose- and time-dependent effect. Saliva also increased the secretion of interleukin 1β, tumor necrosis factor α, prostaglandin E2, and metalloproteinase activity in these cells, which inhibited osteoblastic differentiation.

Conclusion

Submandibular saliva has a biphasic effect on the osteogenic commitment of bone marrow progenitor cells, depending on the concentration and duration of exposure. This finding underscores the active role of saliva in the repair and regeneration of tooth sockets.
雄性大鼠下颌下唾液对骨髓祖细胞体外成骨分化的调节作用。
目的:探讨雄性大鼠下颌下唾液对骨髓祖细胞增殖和成骨分化的影响。设计:收集成年雄性大鼠唾液,测定总蛋白含量。将成年雄性大鼠骨髓祖细胞(BMPC)与不同浓度的唾液蛋白(0至30 µg/mL)孵育,以评估细胞增殖情况。通过测量碱性磷酸酶活性、1型胶原蛋白生成、矿物结节形成和唾液在分化培养基中暴露7、15或21天后分化的分子标记来评估成骨细胞分化。通过检测肿瘤坏死因子- α、白细胞介素- 1 β、前列腺素E2和基质金属蛋白酶2和9来评估唾液对BMPC的促炎作用。结果:低唾液浓度刺激BMPC,促进分泌和增殖状态。相反,在基础条件下,较高的浓度抑制了这两个过程。此外,在成骨培养基中,唾液降低碱性磷酸酶活性、胶原-1生成和BMPC基质矿化,显示出剂量和时间依赖性效应。唾液还增加了这些细胞中白细胞介素1β、肿瘤坏死因子α、前列腺素E2和金属蛋白酶的分泌,从而抑制成骨细胞的分化。结论:颌下腺唾液对骨髓祖细胞的成骨功能具有双相影响,其影响程度取决于唾液的浓度和暴露时间。这一发现强调了唾液在牙槽修复和再生中的积极作用。
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来源期刊
Archives of oral biology
Archives of oral biology 医学-牙科与口腔外科
CiteScore
5.10
自引率
3.30%
发文量
177
审稿时长
26 days
期刊介绍: Archives of Oral Biology is an international journal which aims to publish papers of the highest scientific quality in the oral and craniofacial sciences. The journal is particularly interested in research which advances knowledge in the mechanisms of craniofacial development and disease, including: Cell and molecular biology Molecular genetics Immunology Pathogenesis Cellular microbiology Embryology Syndromology Forensic dentistry
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