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在牵张成骨过程中,单轴静态应变增强了低氧条件下的成骨和成血管潜力。

Uniaxial static strain enhances osteogenic and angiogenic potential under hypoxic conditions in distraction osteogenesis.

机构信息

Department of Oral and Maxillofacial Surgery, Stomatological Hospital, School of Stomatology, Southern Medical University, S366 Jiangnan Boulevard,Haizhu District, Guangzhou City, Guangdong Province, China.

出版信息

J Orthop Surg Res. 2024 Nov 1;19(1):711. doi: 10.1186/s13018-024-05212-x.

Abstract

OBJECTIVE

Bone incision leads to interrupted and sluggish blood flow in the process of distraction osteogenesis (DO), creating a hypoxia (0-2% oxygen tension) at the center of the bone callus. This hypoxia is critical in the coupling of osteogenesis and angiogenesis during DO. This study aimed to investigate the effect of Uniaxial Static Strain (USS) on osteogenesis in osteoblasts under hypoxic conditions, with a focus on the expression of osteogenic markers and angiogenic factors.

METHODS

The USS was made by a multi-unit tension compression device.Osteoblasts were subjected to 10% USS made under hypoxic conditions to mimic the process of DO in vitro. The cell proliferation, alkaline phosphatase (ALP) activity, mineralized nodule formation, and expression of osteogenic and angiogenic markers were evaluated by using a CCK-8 assay, alkaline phosphatase (ALP) staining, ALP activity assay, alizarin red S staining, qRT-PCR, Western blotting and ELISA.

RESULTS

Hypoxia inhibited osteoblast cell proliferation, ALP activity, mineralized nodule formation, and the expression of runt-related transcription factor 2 (Runx- 2), osteopontin(OPN), osteocalcin (OCN), collagen type I (Col1a1). Conversely, hypoxia upregulated the expression of hypoxia-inducible factor 1-alpha (HIF-1α) and vascular endothelial growth factor (VEGF), which are associated with angiogenesis. However, the application of USS enhanced osteoblasts' osteogenic capacity and upregulated angiogenic factors under hypoxic conditions.

CONCLUSION

USS can enhance osteogenesis in osteoblasts under hypoxic conditions. Moreover, it may stimulate angiogenesis by promoting the expression of VEGF, which further contributes to bone formation. This finding provides important implications for understanding the mechanisms involved in bone regeneration and may have clinical applications in optimizing the effectiveness of DO techniques.

摘要

目的

在骨牵张成骨(DO)过程中,骨切开会导致血流中断和缓慢,在骨痂中心产生缺氧(0-2%氧气张力)。这种缺氧对于 DO 过程中成骨和血管生成的偶联至关重要。本研究旨在探讨单轴静态应变(USS)对缺氧条件下成骨细胞成骨的影响,重点研究成骨标志物和血管生成因子的表达。

方法

采用多单元张力压缩装置施加 USS。将成骨细胞置于 10%的 USS 下,在缺氧条件下模拟 DO 的体外过程。通过 CCK-8 检测、碱性磷酸酶(ALP)染色、ALP 活性测定、茜素红 S 染色、qRT-PCR、Western blot 和 ELISA 评估细胞增殖、碱性磷酸酶(ALP)活性、矿化结节形成以及成骨和血管生成标志物的表达。

结果

缺氧抑制成骨细胞增殖、ALP 活性、矿化结节形成以及 runt 相关转录因子 2(Runx-2)、骨桥蛋白(OPN)、骨钙素(OCN)、Ⅰ型胶原(Col1a1)的表达。相反,缺氧上调了与血管生成相关的缺氧诱导因子 1-α(HIF-1α)和血管内皮生长因子(VEGF)的表达。然而,在缺氧条件下,应用 USS 增强了成骨细胞的成骨能力并上调了血管生成因子。

结论

USS 可增强缺氧条件下成骨细胞的成骨能力。此外,它可能通过促进 VEGF 的表达刺激血管生成,从而进一步促进骨形成。这一发现对于理解骨再生过程中的机制具有重要意义,并可能在优化 DO 技术的有效性方面具有临床应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3901/11531187/59828af73406/13018_2024_5212_Fig1_HTML.jpg

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