Baum L, Wiebusch H, Pang C P
Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong, Hong Kong, China.
Microsc Res Tech. 2000 Aug 15;50(4):291-6. doi: 10.1002/1097-0029(20000815)50:4<291::AID-JEMT8>3.0.CO;2-L.
Lipoprotein lipase (LPL) assists lipid transport by transferring lipids between lipoprotein particles and cells. LPL binds apolipoprotein E (apoE) lipoprotein particles and a major apoE receptor, low density lipoprotein receptor related protein (LRP). Because apoE and LRP polymorphisms alter Alzheimer's disease (AD) risk, and LPL itself is found in AD amyloid plaques, we examined whether LPL variants also affect AD risk. In case-control studies in the United States and Canada, the frequencies of two LPL alleles known to affect LPL enzymatic activity were measured in Caucasian AD or elderly normal (N) subjects. Pathologically confirmed subjects in both studies exhibited similar trends toward fewer 447Ter and more 291Ser alleles in AD. Combining results from both countries gave allele frequencies for 447Ter of 13.7% (26/190) in N and 9.4% (80/852) in AD (P = 0.10), and for 291Ser of 0.0% (0/184) in N and 1. 3% (8/636) in AD (P = 0.21). The trend appeared even greater for homozygous 447Ter subjects: 4.2% (4/95) of N vs. 1.4% (6/426) of AD (P = 0.09). These trends are consistent with a putative protective effect of 447Ter and causative effect of 291Ser on AD. Furthermore, brains of AD patients with 447Ter showed trends toward fewer plaques, tangles, and glia, and more neurons and cortical thickness than AD patients without 447Ter. Hippocampal plaques were significantly reduced. LPL might affect hippocampal function and thus dementia via its role as supplier of membrane components or antioxidants to neurons. Alternatively, LPL may play a part in plaque formation through its interaction with apoE and LRP.
脂蛋白脂肪酶(LPL)通过在脂蛋白颗粒与细胞之间转运脂质来辅助脂质运输。LPL结合载脂蛋白E(apoE)脂蛋白颗粒以及一种主要的apoE受体,即低密度脂蛋白受体相关蛋白(LRP)。由于apoE和LRP多态性会改变阿尔茨海默病(AD)风险,且LPL本身存在于AD淀粉样斑块中,我们研究了LPL变体是否也会影响AD风险。在美国和加拿大的病例对照研究中,在白种人AD患者或老年正常(N)受试者中测量了已知会影响LPL酶活性的两个LPL等位基因的频率。两项研究中经病理证实的受试者均呈现出类似趋势,即AD患者中447Ter等位基因较少,291Ser等位基因较多。将两国的结果合并后,N组中447Ter等位基因频率为13.7%(26/190),AD组中为9.4%(80/852)(P = 0.10);N组中291Ser等位基因频率为0.0%(0/184),AD组中为1.3%(8/636)(P = 0.21)。对于纯合447Ter受试者,这种趋势似乎更为明显:N组为4.2%(4/95),AD组为1.4%(6/426)(P = 0.09)。这些趋势与447Ter对AD的假定保护作用以及291Ser对AD的致病作用一致。此外,携带447Ter的AD患者大脑与不携带447Ter的AD患者相比,斑块、缠结和神经胶质细胞较少,神经元和皮质厚度较多的趋势明显。海马体斑块显著减少。LPL可能通过作为神经元膜成分或抗氧化剂的供应者来影响海马体功能,进而影响痴呆。或者,LPL可能通过与apoE和LRP的相互作用在斑块形成中发挥作用。