Department of Physiology, UT Southwestern Medical Center at Dallas, Dallas, Texas 75390-9040, USA.
J Alzheimers Dis. 2010;21(3):781-93. doi: 10.3233/JAD-2010-100159.
Mutations in presenilins 1 and 2 (PS1 and PS2) are responsible for approximately 40% of all early onset familial Alzheimer's disease (FAD) monogenic cases. Presenilins (PSs) function as the catalytic subunit of γ-secretase and support cleavage of the amyloid-β protein precursor (AβPP). We previously discovered that PSs also function as passive endoplasmic reticulum (ER) calcium (Ca2+) leak channels and that most FAD mutations in PSs affected their ER Ca2+ leak function. To further validate the relevance of our findings to human disease, we here performed Ca2+ imaging experiments with lymphoblasts established from FAD patients. We discovered that most FAD mutations in PSs disrupted ER Ca2+ leak function and resulted in increased ER Ca2+ pool in human lymphoblasts. However, we found that a subset of PS1 FAD mutants supported ER Ca2+ leak activity, as ER Ca2+ pool was unaffected in lymphoblasts. Most of the "functional" mutations for ER Ca2+ leak were clustered in the exon 8-9 area of PSEN1 gene and segregated with the cotton wool plaques and spastic paraparesis clinical phenotype occasionally observed in PS1 FAD patients. Our findings with the "functional" and "non-functional" PS1 FAD mutants were confirmed in Ca2+ rescue experiments with PS double-knockout mouse embryonic fibroblasts. Based on the combined effects of the PS1 FAD mutations on ER Ca2+ leak and γ-secretase activities we propose a model that explains the heterogeneity observed in FAD. The proposed model has implications for understanding the pathogenesis of both familial and sporadic AD.
早发型家族性阿尔茨海默病(FAD)的单基因病例中,约有 40%是由早老素 1 和 2(PS1 和 PS2)基因突变引起的。早老素(PSs)作为γ-分泌酶的催化亚基发挥作用,支持淀粉样蛋白-β前体(AβPP)的切割。我们之前发现 PSs 还作为内质网(ER)钙(Ca2+)泄漏通道的被动亚基发挥作用,并且 PS 中的大多数 FAD 突变影响其 ER Ca2+泄漏功能。为了进一步验证我们的发现与人类疾病的相关性,我们在此使用从 FAD 患者建立的淋巴母细胞进行了 Ca2+成像实验。我们发现 PS 中的大多数 FAD 突变破坏了 ER Ca2+泄漏功能,并导致人淋巴母细胞中 ER Ca2+池增加。然而,我们发现 PS1 FAD 突变体的亚组支持 ER Ca2+泄漏活性,因为 ER Ca2+池在淋巴母细胞中不受影响。大多数 ER Ca2+泄漏的“功能性”突变聚集在 PSEN1 基因的外显子 8-9 区域,与偶尔在 PS1 FAD 患者中观察到的棉絮斑和痉挛性截瘫临床表型分离。我们在 PS 双敲除小鼠胚胎成纤维细胞的 Ca2+挽救实验中证实了“功能性”和“非功能性”PS1 FAD 突变体的发现。基于 PS1 FAD 突变对 ER Ca2+泄漏和 γ-分泌酶活性的综合影响,我们提出了一个解释 FAD 中观察到的异质性的模型。该模型对理解家族性和散发性 AD 的发病机制具有重要意义。