Periodontal tissue regeneration with cementogenesis after application of brain‐derived neurotrophic factor in 3‐wall inflamed intra‐bony defect

Author:

Kiyota Mari1,Iwata Tomoyuki1ORCID,Hasegawa Naohiko1,Sasaki Shinya1,Taniguchi Yuri1,Hamamoto Yuta1,Matsuda Shinji1ORCID,Ouhara Kazuhisa1,Takeda Katsuhiro12,Fujita Tsuyoshi1,Kurihara Hidemi1,Kawaguchi Hiroyuki13,Mizuno Noriyoshi1

Affiliation:

1. Department of Periodontal Medicine Hiroshima University Graduate School of Biomedical and Health Sciences Hiroshima Japan

2. Department of Biological Endodontics Hiroshima University Graduate School of Biomedical and Health Sciences Hiroshima Japan

3. Department of General Dentistry Hiroshima University hospital Hiroshima Japan

Abstract

AbstractObjectiveThe purpose of this study is to investigate regenerative process by immunohistochemical analysis and evaluate periodontal tissue regeneration following a topical application of BDNF to inflamed 3‐wall intra‐bony defects.BackgroundBrain‐derived neurotrophic factor (BDNF) plays a role in the survival and differentiation of central and peripheral neurons. BDNF can regulate the functions of non‐neural cells, osteoblasts, periodontal ligament cells, endothelial cells, as well as neural cells. Our previous study showed that a topical application of BDNF enhances periodontal tissue regeneration in experimental periodontal defects of dog and that BDNF stimulates the expression of bone (cementum)‐related proteins and proliferation of human periodontal ligament cells.MethodsSix weeks after extraction of mandibular first and third premolars, 3‐wall intra‐bony defects were created in mandibular second and fourth premolars of beagle dogs. Impression material was placed in all of the artificial defects to induce inflammation. Two weeks after the first operation, BDNF (25 and 50 μg/mL) immersed into atelocollagen sponge was applied to the defects. As a control, only atelocollagen sponge immersed in saline was applied. Two and four weeks after the BDNF application, morphometric analysis was performed. Localizations of osteopontin (OPN) and proliferating cell nuclear antigen (PCNA)‐positive cells were evaluated by immunohistochemical analysis.ResultsTwo weeks after application of BDNF, periodontal tissue was partially regenerated. Immunohistochemical analyses revealed that cells on the denuded root surface were positive with OPN and PCNA. PCNA‐positive cells were also detected in the soft connective tissue of regenerating periodontal tissue. Four weeks after application of BDNF, the periodontal defects were regenerated with cementum, periodontal ligament, and alveolar bone. Along the root surface, abundant OPN‐positive cells were observed. Morphometric analyses revealed that percentage of new cementum length and percentage of new bone area of experimental groups were higher than control group and dose‐dependently increased.ConclusionThese findings suggest that BDNF could induce cementum regeneration in early regenerative phase by stimulating proliferation of periodontal ligament cells and differentiation into periodontal tissue cells, resulting in enhancement of periodontal tissue regeneration in inflamed 3‐wall intra‐bony defects.

Publisher

Wiley

Reference61 articles.

1. Biology and principles of periodontal wound healing/regeneration;Polimeni G;Periodontology,2000

2. Regeneration of periodontal tissues: cementogenesis revisited;Zeichner‐David M;Periodontology,2000

3. A combination of platelet-derived and insulin-like growth factors enhances periodontal regeneration

4. Regeneration of periodontal tissues by basic fibroblast growth factor

5. Periodontal Repair in Dogs: Recombinant Human Bone Morphogenetic Protein-2 Significantly Enhances Periodontal Regeneration

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3