Brookes Steven J, Barron Martin J, Boot-Handford Ray, Kirkham Jennifer, Dixon Michael J
Department of Oral Biology, Leeds Dental Institute, University of Leeds, Clarendon Way, Leeds LS2 9LU, UK.
Hum Mol Genet. 2014 May 1;23(9):2468-80. doi: 10.1093/hmg/ddt642. Epub 2013 Dec 20.
Inherited diseases caused by genetic mutations can arise due to loss of protein function. Alternatively, mutated proteins may mis-fold, impairing endoplasmic reticulum (ER) trafficking, causing ER stress and triggering the unfolded protein response (UPR). The UPR attempts to restore proteostasis but if unsuccessful drives affected cells towards apoptosis. Previously, we reported that in mice, the p.Tyr64His mutation in the enamel extracellular matrix (EEM) protein amelogenin disrupts the secretory pathway in the enamel-forming ameloblasts, resulting in eruption of malformed tooth enamel that phenocopies human amelogenesis imperfecta (AI). Defective amelogenin post-secretory self-assembly and processing within the developing EEM has been suggested to underlie the pathogenesis of X chromosome-linked AI. Here, we challenge this concept by showing that AI pathogenesis associated with the p.Tyr64His amelogenin mutation involves ameloblast apoptosis induced by ER stress. Furthermore, we show that 4-phenylbutyrate can rescue the enamel phenotype in affected female mice by promoting cell survival over apoptosis such that they are able to complete enamel formation despite the presence of the mutation, offering a potential therapeutic option for patients with this form of AI and emphasizing the importance of ER stress in the pathogenesis of this inherited conformational disease.
由基因突变引起的遗传性疾病可能是由于蛋白质功能丧失所致。另外,突变的蛋白质可能会错误折叠,损害内质网(ER)运输,导致内质网应激并触发未折叠蛋白反应(UPR)。UPR试图恢复蛋白质稳态,但如果不成功,就会使受影响的细胞走向凋亡。此前,我们报道在小鼠中,釉质细胞外基质(EEM)蛋白釉原蛋白中的p.Tyr64His突变会破坏成釉细胞中的分泌途径,导致畸形牙釉质萌出,其表现类似于人类牙釉质发育不全(AI)。有研究表明,发育中的EEM内釉原蛋白分泌后自组装和加工缺陷是X染色体连锁AI发病机制的基础。在此,我们对这一概念提出质疑,通过研究表明与p.Tyr64His釉原蛋白突变相关的AI发病机制涉及内质网应激诱导的成釉细胞凋亡。此外,我们还表明,4-苯基丁酸盐可以通过促进细胞存活而非凋亡来挽救受影响雌性小鼠的牙釉质表型,使得它们尽管存在突变仍能够完成牙釉质形成,为患有这种形式AI的患者提供了一种潜在的治疗选择,并强调了内质网应激在这种遗传性构象疾病发病机制中的重要性。