Brookes Steven J, Barron Martin J, Dixon Michael J, Kirkham Jennifer
Division of Oral Biology, School of Dentistry, University of Leeds, St James's University HospitalLeeds, United Kingdom.
Faculty of Biology, Medicine and Health, Manchester Academic Health Sciences Centre, University of ManchesterManchester, United Kingdom.
Front Physiol. 2017 Sep 8;8:653. doi: 10.3389/fphys.2017.00653. eCollection 2017.
During the secretory phase of their life-cycle, ameloblasts are highly specialized secretory cells whose role is to elaborate an extracellular matrix that ultimately confers both form and function to dental enamel, the most highly mineralized of all mammalian tissues. In common with many other "professional" secretory cells, ameloblasts employ the unfolded protein response (UPR) to help them cope with the large secretory cargo of extracellular matrix proteins transiting their ER (endoplasmic reticulum)/Golgi complex and so minimize ER stress. However, the UPR is a double-edged sword, and, in cases where ER stress is severe and prolonged, the UPR switches from pro-survival to pro-apoptotic mode. The purpose of this review is to consider the role of the ameloblast UPR in the biology and pathology of amelogenesis; specifically in respect of amelogenesis imperfecta (AI) and fluorosis. Some forms of AI appear to correspond to classic proteopathies, where pathological intra-cellular accumulations of protein tip the UPR toward apoptosis. Fluorosis also involves the UPR and, while not of itself a classic proteopathic disease, shares some common elements through the involvement of the UPR. The possibility of therapeutic intervention by pharmacological modulation of the UPR in AI and fluorosis is also discussed.
在其生命周期的分泌阶段,成釉细胞是高度特化的分泌细胞,其作用是形成一种细胞外基质,最终赋予牙釉质形态和功能,牙釉质是所有哺乳动物组织中矿化程度最高的。与许多其他“专业”分泌细胞一样,成釉细胞利用未折叠蛋白反应(UPR)来帮助它们应对大量通过内质网/高尔基体复合物转运的细胞外基质蛋白分泌货物,从而将内质网应激降至最低。然而,UPR是一把双刃剑,在严重和长期内质网应激的情况下,UPR会从促生存模式转变为促凋亡模式。本综述的目的是探讨成釉细胞UPR在釉质形成的生物学和病理学中的作用;特别是关于成釉不全(AI)和氟斑牙。某些形式的AI似乎对应于经典的蛋白病,其中蛋白质在细胞内的病理性积累使UPR倾向于凋亡。氟斑牙也涉及UPR,虽然它本身不是一种经典的蛋白病,但通过UPR的参与有一些共同的元素。还讨论了通过药理学调节UPR对AI和氟斑牙进行治疗干预的可能性。