Gronthos S, Mrozik K, Shi S, Bartold P M
Division of Haematology, Mesenchymal Stem Cell Group, Frome Road, Adelaide 5000, SA, Australia.
Calcif Tissue Int. 2006 Nov;79(5):310-7. doi: 10.1007/s00223-006-0040-4. Epub 2006 Oct 10.
Periodontal disease leads to destruction of the connective tissues responsible for restraining teeth within the jaw. To date, various conventional therapies for periodontal regeneration have shown limited and variable clinical outcomes. Recent studies have suggested that newly identified human periodontal ligament stem cells (PDLSCs) may offer an alternate and more reliable strategy for the treatment of periodontal disease using a cell-based tissue engineering approach. In the present study, we generated enriched preparations of PDLSCs derived from ovine periodontal ligament using immunomagnetic bead selection, based on expression of the mesenchymal stem cell-associated antigen CD106 (vascular cell adhesion molecule 1). These CD106+ ovine PDLSCs demonstrated the capacity to form adherent clonogenic clusters of fibroblast-like cells when plated at low densities in vitro. Ex vivo-expanded ovine PDLSCs exhibited a high proliferation rate in vitro and expressed a phenotype (CD44+, CD166+, CBFA-1+, collagen-I+, bone sialoprotein+) consistent with human-derived PDLSCs. Furthermore, cultured ovine PDLSCs expressed high transcript levels of the ligament/tendon-specific early transcription factor scleraxis. Importantly, ex vivo-expanded ovine PDLSCs demonstrated the capacity to regenerate both cementum-like mineral and periodontal ligament when transplanted into NOD/SCID mice. The results from the present study suggest that ovine PDLSCs may potentially be used as a novel cellular therapy to facilitate successful and more predictable regeneration of periodontal tissue using an ovine preclinical model of periodontal disease as a prelude to human clinical studies.
牙周病会导致负责将牙齿固定在颌骨内的结缔组织遭到破坏。迄今为止,各种传统的牙周再生疗法的临床效果有限且参差不齐。最近的研究表明,新发现的人牙周膜干细胞(PDLSCs)可能为采用基于细胞的组织工程方法治疗牙周病提供一种替代且更可靠的策略。在本研究中,我们基于间充质干细胞相关抗原CD106(血管细胞黏附分子1)的表达,利用免疫磁珠分选法从羊牙周膜中制备了富集的PDLSCs制剂。这些CD106 +羊PDLSCs在体外低密度接种时,表现出形成成纤维细胞样细胞的贴壁克隆集落的能力。体外扩增的羊PDLSCs在体外表现出高增殖率,并表达了与人类来源的PDLSCs一致的表型(CD44 +、CD166 +、CBFA - 1 +、胶原蛋白 - I +、骨唾液蛋白 +)。此外,培养的羊PDLSCs表达韧带/肌腱特异性早期转录因子硬骨素的高转录水平。重要的是,体外扩增的羊PDLSCs在移植到NOD/SCID小鼠体内时,表现出再生牙骨质样矿物质和牙周膜的能力。本研究结果表明,羊PDLSCs可能作为一种新型细胞疗法,利用牙周病的羊临床前模型,为人类临床研究做铺垫,促进牙周组织成功且更可预测的再生。