From the Department of Biochemistry, Division of Genome Radiobiology and Medical Science, Graduate School of Biomedical Science, University of Hiroshima, Hiroshima 734-8553, Japan.
J Biol Chem. 2011 Feb 11;286(6):4809-18. doi: 10.1074/jbc.M110.152900. Epub 2010 Dec 6.
To avoid excess accumulation of unfolded proteins in the endoplasmic reticulum (ER), eukaryotic cells have signaling pathways from the ER to the cytosol or nucleus. These processes are collectively termed the ER stress response. Double stranded RNA activated protein kinase (PKR)-like endoplasmic reticulum kinase (PERK) is a major transducer of the ER stress response and directly phosphorylates eIF2α, resulting in translational attenuation. Phosphorylated eIF2α specifically promotes the translation of the transcription factor ATF4. ATF4 plays important roles in osteoblast differentiation and bone formation. Perk(-/-) mice are reported to exhibit severe osteopenia, and the phenotypes observed in bone tissues are very similar to those of Atf4(-/-) mice. However, the involvement of the PERK-eIF2α-ATF4 signaling pathway in osteogenesis is unclear. Phosphorylated eIF2α and ATF4 protein levels were attenuated in Perk(-/-) calvariae, and the gene expression levels of osteocalcin (Ocn) and bone sialoprotein (Bsp), which are targets for ATF4, were also down-regulated. Treatment of wild-type primary osteoblasts with BMP2, which is required for osteoblast differentiation, induced ER stress, leading to an increase in ATF4 protein expression levels. In contrast, the level of ATF4 in Perk(-/-) osteoblasts was severely diminished. The results indicate that PERK signaling is required for ATF4 activation during osteoblast differentiation. Perk(-/-) osteoblasts exhibited decreased alkaline phosphatase activities and delayed mineralized nodule formation relative to wild-type cultures. These abnormalities were almost completely restored by the introduction of ATF4 into Perk(-/-) osteoblasts. Taken together, ER stress occurs during osteoblast differentiation and activates the PERK-eIF2α-ATF4 signaling pathway followed by the promotion of gene expression essential for osteogenesis, such as Ocn and Bsp.
为了避免内质网(ER)中未折叠蛋白的过度积累,真核细胞具有从 ER 到细胞质或细胞核的信号通路。这些过程统称为内质网应激反应。双链 RNA 激活蛋白激酶(PKR)样内质网激酶(PERK)是内质网应激反应的主要传感器,可直接磷酸化 eIF2α,导致翻译衰减。磷酸化的 eIF2α 特异性促进转录因子 ATF4 的翻译。ATF4 在成骨细胞分化和骨形成中发挥重要作用。据报道,Perk(-/-) 小鼠表现出严重的骨质疏松症,并且在骨组织中观察到的表型与 Atf4(-/-) 小鼠非常相似。然而,PERK-eIF2α-ATF4 信号通路在成骨中的参与尚不清楚。Perk(-/-) 颅骨中的磷酸化 eIF2α 和 ATF4 蛋白水平降低,ATF4 的靶基因骨钙素(Ocn)和骨涎蛋白(Bsp)的基因表达水平也下调。用骨形态发生蛋白 2(BMP2)处理野生型原代成骨细胞,BMP2 是成骨细胞分化所必需的,诱导内质网应激,导致 ATF4 蛋白表达水平增加。相比之下,Perk(-/-) 成骨细胞中的 ATF4 水平严重减少。结果表明,PERK 信号在成骨细胞分化过程中激活 ATF4 是必需的。与野生型培养物相比,Perk(-/-) 成骨细胞的碱性磷酸酶活性降低,矿化结节形成延迟。通过将 ATF4 引入 Perk(-/-) 成骨细胞,几乎完全恢复了这些异常。总之,内质网应激发生在成骨细胞分化过程中,并激活 PERK-eIF2α-ATF4 信号通路,随后促进成骨所必需的基因表达,如 Ocn 和 Bsp。