The Pathology of Bone Tissue during Peri-Implantitis

被引:83
作者
Schminke, B. [1 ]
vom Orde, F. [1 ]
Gruber, R. [2 ]
Schliephake, H. [2 ]
Buergers, R. [1 ]
Miosge, N. [1 ]
机构
[1] Univ Gottingen, Tissue Regenerat & Oral Biol Work Grp, Dept Prosthodont, D-37075 Gottingen, Germany
[2] Univ Gottingen, Dept Oral & Maxillofacial Surg, D-37075 Gottingen, Germany
关键词
bone matrix degradation; RUNX2; BMP2; micro array; dental implants; IL8; NONSURGICAL TREATMENT; DIFFERENTIATION; PROTEINS; TITANIUM; FAILURES; THERAPY; CELLS; MODEL;
D O I
10.1177/0022034514559128
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Dental implants are one of the most frequently used treatment options for tooth replacement. Approximately 30% of patients with dental implants develop peri-implantitis, which is an oral inflammatory disease that leads to loss of the supporting tissues, predominately the bone. For the development of future therapeutic strategies, it is essential to understand the molecular pathophysiology of human dental peri-implant infections. Here, we describe the gene and protein expression patterns of peri-implantitis bone tissue compared with healthy peri-implant bone tissue. Furthermore, cells from the osteoblastic lineage derived from peri-implantitis samples were immortalized and characterized. We applied microarray, quantitative reverse transcription polymerase chain reaction, fluorescence-activated cell sorting, and Western blot analyses. The levels of typical bone matrix molecules, including SPP1, BGLAP, and COL9A1, in patients with peri-implantitis were reduced, while the inflammation marker interleukin 8 (IL8) was highly expressed. RUNX2, one of the transcription factors of mature osteoblasts, was also decreased in peri-implantitis. Finally, the human telomerase reverse transcriptase immortalized cell line from peri-implantitis exhibited a more fibro-osteoblastic character than did the healthy control.
引用
收藏
页码:354 / 361
页数:8
相关论文
共 40 条
  • [21] Periimplant diseases: where are we now? - Consensus of the Seventh European Workshop on Periodontology
    Lang, Niklaus P.
    Berglundh, Tord
    [J]. JOURNAL OF CLINICAL PERIODONTOLOGY, 2011, 38 : 178 - 181
  • [22] Microbial findings at failing implants
    Leonhardt, Å
    Renvert, S
    Dahlén, G
    [J]. CLINICAL ORAL IMPLANTS RESEARCH, 1999, 10 (05) : 339 - 345
  • [23] Building strong bones: molecular regulation of the osteoblast lineage
    Long, Fanxin
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2012, 13 (01) : 27 - 38
  • [24] The epidemiology of peri-implantitis
    Mombelli, Andrea
    Mueller, Nada
    Cionca, Norbert
    [J]. CLINICAL ORAL IMPLANTS RESEARCH, 2012, 23 : 67 - 76
  • [25] The novel zinc finger-containing transcription factor Osterix is required for osteoblast differentiation and bone formation
    Nakashima, K
    Zhou, X
    Kunkel, G
    Zhang, ZP
    Deng, JM
    Behringer, RR
    de Crombrugghe, B
    [J]. CELL, 2002, 108 (01) : 17 - 29
  • [26] PALUMBO C, 1990, ACTA ANAT, V137, P350
  • [27] Ex vivo bone morphogenetic protein 2 gene delivery using periodontal ligament stem cells for enhanced re-osseointegration in the regenerative treatment of peri-implantitis
    Park, Shin-Young
    Kim, Kyoung-Hwa
    Gwak, Eun-Hye
    Rhee, Sang-Hoon
    Lee, Jeong-Cheol
    Shin, Seung-Yun
    Koo, Ki-Tae
    Lee, Yong-Moo
    Seol, Yang-Jo
    [J]. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2015, 103 (01) : 38 - 47
  • [28] A new mathematical model for relative quantification in real-time RT-PCR
    Pfaffl, MW
    [J]. NUCLEIC ACIDS RESEARCH, 2001, 29 (09) : E45
  • [29] Non-surgical treatment of peri-implant mucositis and peri-implantitis:: a literature review
    Renvert, Stefan
    Roos-Jansaker, Ann-Marie
    Claffey, Noel
    [J]. JOURNAL OF CLINICAL PERIODONTOLOGY, 2008, 35 : 305 - 315
  • [30] Nine- to fourteen-year follow-up of implant treatment.: Part II:: presence of peri-implant lesions
    Roos-Jansåker, AM
    Lindahl, C
    Renvert, H
    Renvert, S
    [J]. JOURNAL OF CLINICAL PERIODONTOLOGY, 2006, 33 (04) : 290 - 295