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通过与牙周膜来源的成纤维细胞进行细胞间黏附增强间充质干细胞的抗炎和成骨能力

Enhancement of Anti-Inflammatory and Osteogenic Abilities of Mesenchymal Stem Cells via Cell-to-Cell Adhesion to Periodontal Ligament-Derived Fibroblasts.

作者信息

Suzuki Keita, Chosa Naoyuki, Sawada Shunsuke, Takizawa Naoki, Yaegashi Takashi, Ishisaki Akira

机构信息

Division of Cellular Biosignal Sciences, Department of Biochemistry, Iwate Medical University, Yahaba, Iwate 028-3694, Japan; Division of Periodontology, Department of Conservative Dentistry, Iwate Medical University School of Dentistry, Morioka, Iwate 020-8505, Japan.

Division of Cellular Biosignal Sciences, Department of Biochemistry, Iwate Medical University, Yahaba, Iwate 028-3694, Japan.

出版信息

Stem Cells Int. 2017;2017:3296498. doi: 10.1155/2017/3296498. Epub 2017 Jan 12.

Abstract

Mesenchymal stem cells (MSCs) are involved in anti-inflammatory events and tissue repair; these functions are activated by their migration or homing to inflammatory tissues in response to various chemokines. However, the mechanism by which MSCs interact with other cell types in inflammatory tissue remains unclear. We investigated the role of periodontal ligament fibroblasts (PDL-Fs) in regulating the anti-inflammatory and osteogenic abilities of bone marrow-derived- (BM-) MSCs. The expression of monocyte chemotactic protein- (MCP-)1 was significantly enhanced by stimulation of PDL-Fs with inflammatory cytokines. MCP-1 induced the migratory ability of BM-MSCs but not PDL-Fs. Expression levels of anti-inflammatory and inflammatory cytokines were increased and decreased, respectively, by direct-contact coculture between MSCs and PDL-Fs. In addition, the direct-contact coculture enhanced the expression of MSC markers that play important roles in the self-renewal and maintenance of multipotency of MSCs, which in turn induced the osteogenic ability of the cells. These results suggest that MCP-1 induces the migration and homing of BM-MSCs into the PDL inflammatory tissue. The subsequent adherence of MSCs to PDL-Fs plays an immunomodulatory role to terminate inflammation during wound healing and upregulates the expression stem cell markers to enhance the stemness of MSCs, thereby facilitating bone formation in damaged PDL tissue.

摘要

间充质干细胞(MSCs)参与抗炎反应和组织修复;这些功能是通过它们迁移或归巢到炎症组织以响应各种趋化因子而被激活的。然而,MSCs在炎症组织中与其他细胞类型相互作用的机制仍不清楚。我们研究了牙周膜成纤维细胞(PDL-Fs)在调节骨髓来源的(BM-)MSCs的抗炎和成骨能力中的作用。用炎性细胞因子刺激PDL-Fs可显著增强单核细胞趋化蛋白-(MCP-)1的表达。MCP-1诱导BM-MSCs的迁移能力,但不诱导PDL-Fs的迁移能力。通过MSCs与PDL-Fs的直接接触共培养,抗炎和炎性细胞因子的表达水平分别升高和降低。此外,直接接触共培养增强了在MSCs自我更新和多能性维持中起重要作用的MSC标志物的表达,进而诱导了细胞的成骨能力。这些结果表明,MCP-1诱导BM-MSCs迁移并归巢到PDL炎症组织中。随后MSCs与PDL-Fs的黏附在伤口愈合过程中发挥免疫调节作用以终止炎症,并上调干细胞标志物的表达以增强MSCs的干性,从而促进受损PDL组织中的骨形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82a7/5266859/86723622d706/SCI2017-3296498.001.jpg

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