Shao Yankun, Li Miao, Wu Miao, Shi Kai, Fang Boyan, Wang Jie
Department of Neurology, The China-Japan Union Hospital of Jilin University 130033, China.
Department of Neurosurgery, The China-Japan Union Hospital of Jilin University 130033, China.
Int J Clin Exp Med. 2015 Nov 15;8(11):20742-50. eCollection 2015.
We report a PS1 gene mutation (Val 97Leu) in a Chinese familial Alzheimer's disease (FAD) pedigree and a cell model of FAD built by transfecting PS1 v97L mutants into human neuroblastoma SH-SY5Y cells. To test our hypothesis that the PS1 v97L mutation is pathogenic, we investigated possible alterations in transport regulation and intracellular Ca(2+) homeostasis in endoplasmic reticulum (ER). Grp78 is an ER-resident chaperone mediating the unfolded protein response (UPR) and is a key regulator of ER stress transducers. KDEL is a 4-amino-acid retention sequence made of Lys-Asp-Glu-Leu-COO. KDEL is a "resident" sequence as protein residence in ER is consistently associated with KDEL at the C-extremity. Our group used KDEL recognizing anti-Grp78 monoclonal antibody to detect the level of Grp78. We found increased KDEL level in all the transfected cells including cells transfected with PS1 V97L genes, wild-type and the mock. However cells with PS1 V97L mutation expressed a relatively lower KDEL compared with the wild-type and the mock, and a significantly lower Grp78 level compared with the wild-type, the mock and control. These results suggest that PS1 V97L mutation impedes intracellular transport regulation in ER. PS1 V97L mutation mediates increased ER Ca(2+) content in human neuroblastoma SH-SY5Y cells. The increased intracellular Ca(2+) release is due to depleted Ca(2+) storing content of ER but not due to extracellular environment as capacitative Ca(2+) entry (CCE) is invariant. PS1 V97L mutation interferes with intracellular Ca(2+) homeostasis. Abnormal transport regulation and Ca(2+) homeostasis attributed to PS1 V97L mutation may be associated with the pathology of Chinese familial FAD.
我们报道了一个中国家族性阿尔茨海默病(FAD)家系中的PS1基因突变(Val 97Leu),以及通过将PS1 v97L突变体转染到人神经母细胞瘤SH-SY5Y细胞构建的FAD细胞模型。为了验证我们关于PS1 v97L突变具有致病性的假设,我们研究了内质网(ER)中转运调节和细胞内Ca(2+)稳态的可能改变。Grp78是一种内质网驻留伴侣蛋白,介导未折叠蛋白反应(UPR),是内质网应激传感器的关键调节因子。KDEL是由Lys-Asp-Glu-Leu-COO组成的四氨基酸保留序列。KDEL是一个“驻留”序列,因为内质网中的蛋白质驻留始终与C末端的KDEL相关。我们小组使用识别KDEL的抗Grp78单克隆抗体来检测Grp78的水平。我们发现所有转染细胞中的KDEL水平都有所增加,包括转染PS1 V97L基因、野生型和空载体的细胞。然而,与野生型和空载体相比,具有PS1 V97L突变的细胞表达的KDEL相对较低,与野生型、空载体和对照相比,Grp78水平显著较低。这些结果表明,PS1 V97L突变阻碍了内质网中的细胞内转运调节。PS1 V97L突变介导人神经母细胞瘤SH-SY5Y细胞内质网Ca(2+)含量增加。细胞内Ca(2+)释放增加是由于内质网Ca(2+)储存含量减少,而不是由于细胞外环境,因为钙池操纵性Ca(2+)内流(CCE)不变。PS1 V97L突变干扰细胞内Ca(2+)稳态。PS1 V97L突变导致的异常转运调节和Ca(2+)稳态可能与中国家族性FAD的病理有关。