[Aβ Receptor PirB and its regulation by LOTUS].

Yuki Kawaguchi, Kohtaro Takei
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引用次数: 0

Abstract

Over the years, research has accumulated a vast amount of knowledge about the pathogenesis of dementia, including Alzheimer's disease (AD). However, fundamental treatments for AD have not yet been established. In this article, we discuss an Aβ receptor, paired immunoglobulin like receptor B (PirB) and its endogenous regulator lateral olfactory tract usher substance (LOTUS), which are completely different novel drug target from existing drugs, and the possibility of endogenous inhibitors of PirB. PirB expressed in neurons is a negative regulator of neuronal plasticity, as loss or inhibition of PirB increases neuronal plasticity, leading to increased spine density and improved cognitive function. Furthermore, PirB is known to function as a receptor for Aβ, leading to reduced neuronal plasticity and cell death. These findingss suggest that PirB can be positioned as a novel drug target for the treatment of AD. The neuronal circuit-forming factor LOTUS, which binds to PirB and functions as an endogenous antagonist, has been shown to inhibit the neurotoxic effects of Aβ mediated by PirB. Namely, LOTUS is an endogenous molecule that inhibits Aβ receptor function of PirB and may have medicinal effects against Aβ pathology.

[Aβ受体PirB及其LOTUS调控]。
多年来,研究积累了大量关于痴呆症发病机制的知识,包括阿尔茨海默病(AD)。然而,阿尔茨海默病的基本治疗方法尚未建立。本文讨论了Aβ受体、配对免疫球蛋白样受体B(配对免疫球蛋白样受体B,配对免疫球蛋白样受体B,配对免疫球蛋白样受体B,配对免疫球蛋白样受体B及其内源性调节物外侧嗅道诱导物质(LOTUS)这两种与现有药物完全不同的新型药物靶点,以及内源性抑制免疫球蛋白样受体B的可能性。PirB在神经元中的表达是神经元可塑性的负调节因子,因为PirB的缺失或抑制会增加神经元的可塑性,从而导致脊柱密度增加和认知功能改善。此外,PirB被认为是a β的受体,导致神经元可塑性降低和细胞死亡。这些发现提示PirB可以定位为治疗AD的新型药物靶点。神经元回路形成因子LOTUS与PirB结合并作为内源性拮抗剂起作用,已被证明可以抑制由PirB介导的Aβ的神经毒性作用。即,LOTUS是抑制PirB的Aβ受体功能的内源性分子,可能对Aβ病理有一定的药理作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Folia Pharmacologica Japonica
Folia Pharmacologica Japonica Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
0.40
自引率
0.00%
发文量
132
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