Lossdörfer S, Fiekens D, Salik M I, Götz W, Jäger A
Department of Orthodontics, Dental Clinic, University of Bonn, Bonn, Germany.
J Periodontal Res. 2008 Oct;43(5):563-9. doi: 10.1111/j.1600-0765.2008.01087.x. Epub 2008 Jul 4.
Although periodontal ligament cells display several osteoblastic traits, their phenotypic expression is still not well established. It remains a matter of debate whether they resemble a terminally differentiated cell type or an intermediate maturation state that potentially can be directed towards a fibroblastic or an osteoblastic phenotype.
To explore the characteristics of periodontal ligament cells in greater detail, fourth-passage, sixth-passage and eighth-passage human periodontal ligament cells were cultured for up to 3 wk. Ki-67, alkaline phosphatase, osteocalcin, osteoprotegerin and receptor activator of nuclear factor-kappaB ligand (RANKL) mRNA expression was quantified by real-time polymerase chain reaction. Furthermore, the cellular response to fibroblast growth factor-2 and bone morphogenetic protein-7 was examined in first-passage and fourth-passage cells. Dermal fibroblasts (1BR.3.G) and osteoblast-like cells (MG63) served as reference cell lines.
Proliferation decreased over time and was highest in fourth-passage cells. The expression of differentiation parameters, osteoprotegerin and RANKL increased with culture time and was higher in fourth-passage cells than in cells of later passages. The RANKL/osteoprotegerin ratio increased steadily until day 21. Administration of fibroblast growth factor-2 enhanced cell numbers in both passages, whereas alkaline phosphatase and osteocalcin production remained unchanged. By contrast, exposure of periodontal ligament cells to bone morphogenetic protein-7 resulted in a reduction of cell number in the first and fourth passages, whereas the production of alkaline phosphatase and osteocalcin was enhanced. In dermal fibroblasts, differentiation parameters did not respond to both stimuli. MG63 cells behaved similarly to periodontal ligament cells.
These results indicate that subculture affects the phenotypic expression of human periodontal ligament cells with respect to the characteristics that these cells share with osteoblasts. Furthermore, the periodontal ligament cell phenotype can be altered by fibroblastic and osteoblastic growth factors.
尽管牙周膜细胞表现出多种成骨细胞特征,但其表型表达仍未完全明确。它们是类似于终末分化细胞类型还是潜在可导向成纤维细胞或成骨细胞表型的中间成熟状态,仍存在争议。
为更详细地探究牙周膜细胞的特征,对第四代、第六代和第八代人牙周膜细胞进行长达3周的培养。通过实时聚合酶链反应定量检测Ki-67、碱性磷酸酶、骨钙素、骨保护素和核因子κB受体激活剂配体(RANKL)的mRNA表达。此外,在第一代和第四代细胞中检测了细胞对成纤维细胞生长因子-2和骨形态发生蛋白-7的反应。真皮成纤维细胞(1BR.3.G)和成骨样细胞(MG63)作为对照细胞系。
增殖随时间下降,在第四代细胞中最高。分化参数、骨保护素和RANKL的表达随培养时间增加,且第四代细胞中的表达高于后续代次的细胞。RANKL/骨保护素比值在第21天前稳步上升。成纤维细胞生长因子-2处理使两代细胞数量均增加,而碱性磷酸酶和骨钙素的产生保持不变。相比之下,牙周膜细胞暴露于骨形态发生蛋白-7导致第一代和第四代细胞数量减少,而碱性磷酸酶和骨钙素的产生增加。在真皮成纤维细胞中,分化参数对两种刺激均无反应。MG63细胞的表现与牙周膜细胞相似。
这些结果表明,传代培养会影响人牙周膜细胞与成骨细胞共有的表型表达特征。此外,牙周膜细胞表型可被成纤维细胞生长因子和成骨细胞生长因子改变。