Oral Biology, School of Dentistry, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Exp Cell Res. 2012 Nov 1;318(18):2397-406. doi: 10.1016/j.yexcr.2012.07.008. Epub 2012 Jul 20.
The present study aimed to determine whether dentine tissue and preparations of extracellular matrix (ECM) from pulp (pECM) and dentine (dECM), and breakdown products, influenced pulp cell migration. Chemotaxis transwell and agarose spot assays demonstrated that both dentine and pulp ECM molecules acted as chemoattractants for primary pulp cells. Chemoattractant activities of dECM and pECM were enhanced when subjected to acid and enzymatic breakdown, respectively. This enhanced activity following physiologically relevant breakdown may be pertinent to the disease environment. Pulp cell migration in response to dental ECMs was dependent on an active rho pathway. Recruited cells exhibited increased stem cell marker expression indicating that dental ECMs and their breakdown products selectively attract progenitor cells that contribute to repair processes. In conclusion, combined these results indicate that ECM molecules contribute to cell recruitment necessary for regeneration of the dentine-pulp complex after injury.
本研究旨在确定牙髓组织和细胞外基质(ECM)的制备物(pECM 和 dECM)以及其降解产物是否影响牙髓细胞的迁移。趋化性 Transwell 和琼脂糖斑点分析表明,牙本质和牙髓 ECM 分子均作为原发性牙髓细胞的趋化因子。牙本质和牙髓 ECM 的趋化活性在分别进行酸和酶分解后增强。这种生理相关的分解后增强的活性可能与疾病环境有关。牙髓细胞对牙 ECM 的迁移依赖于活跃的 rho 途径。募集的细胞表现出增加的干细胞标志物表达,表明牙 ECM 及其降解产物选择性地吸引有助于修复过程的祖细胞。总之,这些结果表明 ECM 分子有助于损伤后牙本质牙髓复合体再生所必需的细胞募集。