Mattson M P, Guo Q, Furukawa K, Pedersen W A
Department of Anatomy and Neurobiology, University of Kentucky, Lexington 40536-0230, USA.
J Neurochem. 1998 Jan;70(1):1-14. doi: 10.1046/j.1471-4159.1998.70010001.x.
Many cases of autosomal dominant inherited forms of early-onset Alzheimer's disease are caused by mutations in the genes encoding presenilin-1 (PS-1; chromosome 14) and presenilin-2 (PS-2; chromosome 1). PSs are expressed in neurons throughout the brain wherein they appear to be localized primarily to the endoplasmic reticulum (ER) of cell bodies and dendrites. PS-1 and PS-2 show high homology and are predicted to have eight transmembrane domains with the C terminus, N terminus, and a loop domain all on the cytosolic side of the membrane; an enzymatic cleavage of PSs occurs at a site near the loop domain. The normal function of PSs is unknown, but data suggest roles in membrane trafficking, amyloid precursor protein processing, and regulation of ER calcium homeostasis. Homology of PSs to the C. elegans gene sel-12, which is involved in Notch signaling, and phenotypic similarities of PS-1 and Notch knockout mice suggest a developmental role for PSs in the nervous system. When expressed in cultured cells and transgenic mice, mutant PSs promote increased production of a long form of amyloid beta-peptide (A beta1-42) that may possess enhanced amyloidogenic and neurotoxic properties. PS mutations sensitize cultured neural cells to apoptosis induced by trophic factor withdrawal, metabolic insults, and amyloid beta-peptide. The mechanism responsible for the proapoptotic action of mutant PSs may involve perturbed calcium release from ER stores and increased levels of oxidative stress. Recent studies of apoptosis in many different cell types suggest that ER calcium signaling can modulate apoptosis. The evolving picture of PS roles in neuronal plasticity and Alzheimer's disease is bringing to the forefront the ER, an organelle increasingly recognized as a key regulator of neuronal plasticity and survival.
许多常染色体显性遗传的早发性阿尔茨海默病病例是由编码早老素-1(PS-1;14号染色体)和早老素-2(PS-2;1号染色体)的基因突变引起的。早老素在整个大脑的神经元中表达,在那里它们似乎主要定位于细胞体和树突的内质网(ER)。PS-1和PS-2显示出高度同源性,预计有八个跨膜结构域,其C端、N端和一个环结构域都在膜的胞质侧;早老素的酶切发生在环结构域附近的一个位点。早老素的正常功能尚不清楚,但数据表明其在膜运输、淀粉样前体蛋白加工和内质网钙稳态调节中起作用。早老素与参与Notch信号传导的秀丽隐杆线虫基因sel-12的同源性,以及PS-1和Notch基因敲除小鼠的表型相似性表明早老素在神经系统发育中起作用。当在培养细胞和转基因小鼠中表达时,突变的早老素会促进一种长形式的淀粉样β肽(Aβ1-42)产量增加,这种肽可能具有增强的淀粉样生成和神经毒性特性。PS突变使培养的神经细胞对营养因子撤除、代谢损伤和淀粉样β肽诱导的凋亡敏感。突变早老素促凋亡作用的机制可能涉及内质网钙库钙释放紊乱和氧化应激水平升高。最近对许多不同细胞类型凋亡的研究表明,内质网钙信号可以调节凋亡。早老素在神经元可塑性和阿尔茨海默病中作用的不断演变,使内质网成为焦点,内质网这个细胞器越来越被认为是神经元可塑性和存活的关键调节因子。