Călin C, Sajin M, Moldovan V T, Coman C, Stratul S I, Didilescu A C
Division of Embryology, Faculty of Dental Medicine, Carol Davila University of Medicine and Pharmacy, Romania.
Chair of Pathology, Faculty of Medicine, Carol Davila University of Medicine and Pharmacy, Romania.
Ann Anat. 2021 May;235:151674. doi: 10.1016/j.aanat.2020.151674. Epub 2021 Jan 2.
Extracellular matrix molecules (ECMM) expression during tertiary dentinogenesis provides useful information for regenerative applications and efficacy of pulp capping materials.
To identify and review the expression and roles of non-collagenous ECMM after successful direct pulp capping (DPC), following mechanical pulp exposures, via immunohistochemistry (IHC). The study addressed the question of where will successful DPC impact the IHC expression of these molecules.
In vivo animal and human original clinical studies reporting on ECMM in relation to different follow-up periods were screened and evaluated via descriptive analysis. The electronic literature search was carried out in three databases (MEDLINE/PubMed, Web of Science, Scopus), followed by manual screening of relevant journals and cross-referencing, up to December 2018.
STUDY ELIGIBILITY CRITERIA, PARTICIPANTS, AND INTERVENTIONS: Randomized and non-randomized controlled trials, conducted in humans and animals, were selected. Histological evidence for tertiary dentine formation was a prerequisite for IHC evaluation.
The methodological quality of the included articles was independently assessed using the Systematic Review Centre for Laboratory animal Experimentation (SYRCLE) and the Cochrane risk of bias tool (RoB 1), respectively.
From a total of 1534 identified studies, 18 were included. Thirteen papers evaluated animal subjects and five studies were carried out on humans. In animals and humans, fibronectin and tenascin expressions were detected in pulp and odontoblast-like cells (OLC); dentine sialoprotein was expressed in both soft and newly-formed mineralized tissue. In animals, bone sialoprotein was early expressed, in association with OLC and predentin; the immunoreactivity for dentine sialophosphoprotein and dentine matrix protein-1 was associated with the OLC and dentine bridge; osteopontin was expressed in OLC, predentine and reparative dentine. A considerable heterogeneity was found in the methodologies of the included studies, as well as interspecies variability of results in terms of time.
Within the limited scientific evidence, all non-collagenous ECMM expressions during tertiary dentinogenesis are active and related to soft and hard tissues. There is a shortage of human studies, and future research directions should focus more on them. PROSPERO Protocol: CRD42019121304.
第三期牙本质形成过程中细胞外基质分子(ECMM)的表达为再生应用和牙髓盖髓材料的疗效提供了有用信息。
通过免疫组织化学(IHC)鉴定和综述机械性牙髓暴露后成功直接盖髓(DPC)后非胶原ECMM的表达及作用。该研究探讨了成功的DPC会在何处影响这些分子的IHC表达这一问题。
通过描述性分析筛选和评估了报告不同随访期ECMM的体内动物和人类原始临床研究。在三个数据库(MEDLINE/PubMed、Web of Science、Scopus)中进行电子文献检索,随后人工筛选相关期刊并交叉引用,截至2018年12月。
研究入选标准、参与者和干预措施:选择在人类和动物中进行的随机和非随机对照试验。第三期牙本质形成的组织学证据是IHC评估的先决条件。
分别使用实验动物系统评价中心(SYRCLE)和Cochrane偏倚风险工具(RoB 1)独立评估纳入文章的方法学质量。
在总共1534项已识别研究中,纳入了18项。13篇论文评估了动物受试者,5项研究在人类中进行。在动物和人类中,纤连蛋白和腱生蛋白在牙髓和成牙本质样细胞(OLC)中被检测到;牙本质涎蛋白在软组织和新形成的矿化组织中均有表达。在动物中,骨涎蛋白早期表达,与OLC和前期牙本质相关;牙本质涎磷蛋白和牙本质基质蛋白-1的免疫反应性与OLC和牙本质桥相关;骨桥蛋白在OLC、前期牙本质和修复性牙本质中表达。在所纳入研究的方法学以及结果在时间方面存在相当大的种间变异性方面发现了相当大的异质性。
在有限的科学证据范围内,第三期牙本质形成过程中所有非胶原ECMM的表达都是活跃的,并与软组织和硬组织相关。人类研究不足,未来的研究方向应更多地关注它们。PROSPERO方案:CRD42019121304。