Rufas Pierre, Jeanneau Charlotte, Rombouts Charlotte, Laurent Patrick, About Imad
Aix Marseille Université, CNRS, ISM, Institute of Movement Sciences, Marseille, France.
Aix Marseille Université, CNRS, ISM, Institute of Movement Sciences, Marseille, France; APHM, Service d'Odontologie, Hôpital Timone, Marseille, France.
J Endod. 2016 Sep;42(9):1377-84. doi: 10.1016/j.joen.2016.06.011. Epub 2016 Aug 3.
Complement activation is considered a major mechanism in innate immunity. Although it is mainly involved in initiating inflammation, recent data reported its involvement in other processes such as tissue regeneration. In the dental pulp, complement C5a fragment has been shown to be involved in the recruitment of dental pulp stem cells (DPSCs). This study sought to investigate the possible role of C3a, another complement fragment, in the early steps of dentin-pulp regeneration.
Expression of C3a receptor (C3aR) was investigated by immunofluorescence and reverse transcriptase polymerase chain reaction on cultured pulp fibroblasts, STRO-1-sorted DPSCs, as well as on human tooth sections in vivo. The effect of C3a on proliferation of both DPSCs and pulp fibroblasts was investigated by MTT assay. Cell migration under a C3a gradient was investigated by using microfluidic chemotaxis chambers.
C3aR was expressed in vivo as well as in cultured pulp fibroblasts co-expressing fibroblast surface protein and in DPSCs co-expressing STRO-1. Addition of recombinant C3a induced a significant proliferation of both cell types. When subjected to a C3a gradient, DPSCs were mobilized but not specifically recruited, whereas pulp fibroblasts were specifically recruited following a C3a gradient.
These results provide the first demonstration of C3aR expression in the dental pulp and demonstrate that C3a is involved in increasing DPSCs and fibroblast proliferation, in mobilizing DPSCs, and in specifically guiding fibroblast recruitment. This provides an additional link to the tight correlation between inflammation and tissue regeneration.
补体激活被认为是固有免疫中的一种主要机制。尽管它主要参与引发炎症,但最近的数据表明其还参与其他过程,如组织再生。在牙髓中,补体C5a片段已被证明参与牙髓干细胞(DPSC)的募集。本研究旨在探讨另一种补体片段C3a在牙本质-牙髓再生早期阶段可能发挥的作用。
通过免疫荧光和逆转录聚合酶链反应,对培养的牙髓成纤维细胞、经STRO-1分选的DPSC以及体内的人牙切片进行C3a受体(C3aR)表达的研究。通过MTT法研究C3a对DPSC和成纤维细胞增殖的影响。使用微流控趋化室研究在C3a梯度下的细胞迁移。
C3aR在体内以及共表达成纤维细胞表面蛋白的培养牙髓成纤维细胞和共表达STRO-1的DPSC中均有表达。添加重组C3a可诱导这两种细胞类型显著增殖。当处于C3a梯度中时,DPSC被动员但未被特异性募集,而牙髓成纤维细胞在C3a梯度下被特异性募集。
这些结果首次证明了C3aR在牙髓中的表达,并表明C3a参与增加DPSC和成纤维细胞的增殖、动员DPSC以及特异性引导成纤维细胞的募集。这为炎症与组织再生之间的紧密关联提供了又一联系。