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顺-9, 反-11-十八碳二烯酸(共轭亚油酸的一种异构体)抑制神经元中淀粉样β肽的分泌。

Suppression of amyloid-β secretion from neurons by cis-9, trans-11-octadecadienoic acid, an isomer of conjugated linoleic acid.

机构信息

Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Japan.

Laboratory of Neuroscience, Graduate School of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.

出版信息

J Neurochem. 2021 Nov;159(3):603-617. doi: 10.1111/jnc.15490. Epub 2021 Aug 25.

Abstract

Two common conjugated linoleic acids (LAs), cis-9, trans-11 CLA (c9,t11 CLA) and trans-10, cis-12 CLA (t10,c12 CLA), exert various biological activities. However, the effect of CLA on the generation of neurotoxic amyloid-β (Aβ) protein remains unclear. We found that c9,t11 CLA significantly suppressed the generation of Aβ in mouse neurons. CLA treatment did not affect the level of β-site APP-cleaving enzyme 1 (BACE1), a component of active γ-secretase complex presenilin 1 amino-terminal fragment, or Aβ protein precursor (APP) in cultured neurons. BACE1 and γ-secretase activities were not directly affected by c9,t11 CLA. Localization of BACE1 and APP in early endosomes increased in neurons treated with c9,t11 CLA; concomitantly, the localization of both proteins was reduced in late endosomes, the predominant site of APP cleavage by BACE1. The level of CLA-containing phosphatidylcholine (CLA-PC) increased dramatically in neurons incubated with CLA. Incorporation of phospholipids containing c9,t11 CLA, but not t10,c12 CLA, into the membrane may affect the localization of some membrane-associated proteins in intracellular membrane compartments. Thus, in neurons treated with c9,t11 CLA, reduced colocalization of APP with BACE1 in late endosomes may decrease APP cleavage by BACE1 and subsequent Aβ generation. Our findings suggest that the accumulation of c9,t11 CLA-PC/LPC in neuronal membranes suppresses the production of neurotoxic Aβ in neurons.

摘要

两种常见的共轭亚油酸(CLA),顺式-9,反式-11 CLA(c9,t11 CLA)和反式-10,顺式-12 CLA(t10,c12 CLA),具有多种生物学活性。然而,CLA 对神经毒性淀粉样β(Aβ)蛋白产生的影响尚不清楚。我们发现 c9,t11 CLA 可显著抑制小鼠神经元中 Aβ的产生。CLA 处理不影响β位 APP 切割酶 1(BACE1)的水平,BACE1 是活性 γ-分泌酶复合物早老素 1氨基末端片段的组成部分,或在培养的神经元中 Aβ蛋白前体(APP)。c9,t11 CLA 不直接影响 BACE1 和 γ-分泌酶的活性。BACE1 和 APP 在早期内体中的定位在用 c9,t11 CLA 处理的神经元中增加;同时,两种蛋白质在晚期内体中的定位减少,BACE1 主要切割 APP 的部位。CLA 含有磷脂酰胆碱(CLA-PC)的水平在孵育有 CLA 的神经元中急剧增加。含有 c9,t11 CLA 的磷脂的掺入,而不是 t10,c12 CLA,进入膜中可能会影响某些膜相关蛋白在细胞内膜隔室中的定位。因此,在用 c9,t11 CLA 处理的神经元中,APP 与 BACE1 在晚期内体中的共定位减少可能会减少 BACE1 对 APP 的切割和随后 Aβ的产生。我们的发现表明,神经元膜中 c9,t11 CLA-PC/LPC 的积累抑制了神经元中神经毒性 Aβ的产生。

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