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转录因子与骨髓基质细胞在牙种植体骨整合中的作用

Transcription factor and bone marrow stromal cells in osseointegration of dental implants.

机构信息

Division of Oral Biology, Tufts University School of Dental Medicine, One Kneeland Street, Boston MA, 02111,

出版信息

Eur Cell Mater. 2013 Dec 19;26:263-70; discussion 270-1. doi: 10.22203/ecm.v026a19.

Abstract

Titanium implants are widely used in dental clinics and orthopaedic surgery. However, bone formation surrounding the implant is relatively slow after inserting the implant. The current study assessed the effects of bone marrow stromal cells (BMSCs) with forced expression of special AT-rich sequence-binding protein 2 (SATB2) on the osseointegration of titanium implants. To determine whether SATB2 overexpression in BMSCs can enhance the osseointegration of implants, BMSCs were infected with the retrovirus encoding Satb2 (pBABE-Satb2) and were locally applied to bone defects before implanting the titanium implants in the mouse femur. Seven and twenty-one days after implantation, the femora were isolated for immunohistochemical (IHC) staining, haematoxylin eosin (H&E) staining, real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR), and micro-computed tomography (μCT) analysis. IHC staining analysis revealed that SATB2-overexpressing BMSCs were intensely distributed in the bone tissue surrounding the implant. Histological analysis showed that SATB2-overexpressing BMSCs significantly enhanced new bone formation and bone-to-implant contact 3 weeks after implantation. Real-time qRT-PCR results showed that the local delivery of SATB2-overexpressing BMSCs enhanced expression levels of potent osteogenic transcription factors and bone matrix proteins in the implantation sites. μCT analysis demonstrated that SATB2-overexpressing BMSCs significantly increased the density of the newly formed bone surrounding the implant 3 weeks post-operatively. These results conclude that local delivery of SATB2-overexpressing BMSCs significantly accelerates osseointegration of titanium implants. These results provide support for future pharmacological and clinical applications of SATB2, which accelerates bone regeneration around titanium implants.

摘要

钛植入物在牙科诊所和矫形外科中被广泛应用。然而,在植入植入物后,周围骨的形成相对较慢。本研究评估了强制表达特殊富含 AT 序列结合蛋白 2(SATB2)的骨髓基质细胞(BMSCs)对钛植入物骨整合的影响。为了确定 BMSCs 中 SATB2 的过表达是否可以增强植入物的骨整合,用编码 Satb2 的逆转录病毒(pBABE-Satb2)感染 BMSCs,并在将钛植入物植入小鼠股骨前将其局部应用于骨缺损。植入后 7 天和 21 天,分离股骨进行免疫组织化学(IHC)染色、苏木精-伊红(H&E)染色、实时定量逆转录聚合酶链反应(qRT-PCR)和微计算机断层扫描(μCT)分析。IHC 染色分析显示,SATB2 过表达的 BMSCs 在植入物周围的骨组织中强烈分布。组织学分析表明,SATB2 过表达的 BMSCs 显著增强了植入后 3 周时的新骨形成和骨-植入物接触。实时 qRT-PCR 结果显示,SATB2 过表达的 BMSCs 增强了植入部位的潜在成骨转录因子和骨基质蛋白的表达水平。μCT 分析表明,SATB2 过表达的 BMSCs 显著增加了术后 3 周时植入物周围新形成骨的密度。这些结果表明,局部递送 SATB2 过表达的 BMSCs 可显著加速钛植入物的骨整合。这些结果为 SATB2 加速钛植入物周围骨再生的未来药理学和临床应用提供了支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f37b/7700752/4dd9df3783e6/nihms-1646990-f0001.jpg

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