Lyngstadaas S P, Lundberg E, Ekdahl H, Andersson C, Gestrelius S
Department Research and Development, Biora AB, Malmö, Sweden.
J Clin Periodontol. 2001 Feb;28(2):181-8. doi: 10.1034/j.1600-051x.2001.028002181.x.
Enamel extracellular matrix proteins in the form of the enamel matrix derivative EMDOGAIN (EMD) have been successfully employed to mimic natural cementogenesis to restore fully functional periodontal ligament, cementum and alveolar bone in patients with severe periodontitis. When applied to denuded root surfaces EMD forms a matrix that locally facilitates regenerative responses in the adjacent periodontal tissues. The cellular mechanism(s), e.g. autocrine growth factors, extracellular matrix synthesis and cell growth, underlying PDL regeneration with EMD is however poorly investigated.
Human periodontal ligament (PDL) cells were cultured on EMD and monitored for cellular attachment rate, proliferation, DNA replication and metabolism. Furthermore, intracellular cyclic-AMP levels and autocrine production of selected growth factors were monitored by immunological assays. Controls included PDL and epithelial cells in parallel cultures.
PDL cell attachment rate, growth and metabolism were all significantly increased when EMD was present in cultures. Also, cells exposed to EMD showed increased intracellular cAMP signalling and autocrine production of TGF-beta1, IL-6 and PDGF AB when compared to controls. Epithelial cells increased cAMP and PDGF AB secretion when EMD was present, but proliferation and growth were inhibited.
Cultured PDL cells exposed to EMD increase attachment rate, growth rate and metabolism, and subsequently release several growth factors into the medium. The cellular interaction with EMD generates an intracellular cAMP signal, after which cells secrete TGF-beta1, IL-6 and PDGF AB. Epithelial cell growth however, is inhibited by the same signal. This suggest that EMD favours mesenchymal cell growth over epithelium, and that autocrine growth factors released by PDL cells exposed to EMD contribute to periodontal healing and regeneration in a process mimicking natural root development.
牙釉质基质衍生物EMDOGAIN(EMD)形式的牙釉质细胞外基质蛋白已成功用于模拟天然牙骨质生成,以恢复重度牙周炎患者的全功能牙周韧带、牙骨质和牙槽骨。当应用于裸露的牙根表面时,EMD形成一种基质,局部促进相邻牙周组织的再生反应。然而,关于EMD促进牙周韧带再生的细胞机制,如自分泌生长因子、细胞外基质合成和细胞生长,研究较少。
将人牙周韧带(PDL)细胞培养在EMD上,并监测细胞附着率、增殖、DNA复制和代谢。此外,通过免疫测定法监测细胞内环磷酸腺苷(cAMP)水平和选定生长因子的自分泌产生。对照组包括平行培养的PDL细胞和上皮细胞。
当培养物中存在EMD时,PDL细胞的附着率、生长和代谢均显著增加。此外,与对照组相比,暴露于EMD的细胞显示细胞内cAMP信号增加,以及TGF-β1、IL-6和PDGF AB的自分泌产生。当存在EMD时,上皮细胞的cAMP和PDGF AB分泌增加,但增殖和生长受到抑制。
暴露于EMD的培养PDL细胞增加附着率、生长速率和代谢,随后将几种生长因子释放到培养基中。细胞与EMD的相互作用产生细胞内cAMP信号,之后细胞分泌TGF-β1、IL-6和PDGF AB。然而,上皮细胞的生长受到相同信号的抑制。这表明EMD更有利于间充质细胞生长而非上皮细胞生长,并且暴露于EMD的PDL细胞释放的自分泌生长因子在模拟天然牙根发育的过程中有助于牙周愈合和再生。