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高胆固醇饮食通过增强大鼠脑中磷脂酶 C(PLCβ1)的表达降低磷脂酰肌醇 4,5-二磷酸水平。

High-Cholesterol Diet Decreases the Level of Phosphatidylinositol 4,5-Bisphosphate by Enhancing the Expression of Phospholipase C (PLCβ1) in Rat Brain.

机构信息

Department of Physiology, Sungkyunkwan University School of Medicine, Suwon, Gyeonggi-do 16419, Korea.

出版信息

Int J Mol Sci. 2020 Feb 10;21(3):1161. doi: 10.3390/ijms21031161.

Abstract

Cholesterol is a critical component of eukaryotic membranes, where it contributes to regulating transmembrane signaling, cell-cell interaction, and ion transport. Dysregulation of cholesterol levels in the brain may induce neurodegenerative diseases, such as Alzheimer's disease, Parkinson disease, and Huntington disease. We previously reported that augmenting membrane cholesterol level regulates ion channels by decreasing the level of phosphatidylinositol 4,5-bisphosphate (PIP), which is closely related to β-amyloid (Aβ) production. In addition, cholesterol enrichment decreased PIP levels by increasing the expression of the β1 isoform of phospholipase C (PLC) in cultured cells. In this study, we examined the effect of a high-cholesterol diet on phospholipase C (PLCβ1) expression and PIP levels in rat brain. PIP levels were decreased in the cerebral cortex in rats on a high-cholesterol diet. Levels of PLCβ1 expression correlated with PIP levels. However, cholesterol and PIP levels were not correlated, suggesting that PIP level is regulated by cholesterol via PLCβ1 expression in the brain. Thus, there exists cross talk between cholesterol and PIP that could contribute to the pathogenesis of neurodegenerative diseases.

摘要

胆固醇是真核细胞膜的重要组成部分,有助于调节跨膜信号转导、细胞间相互作用和离子转运。大脑中胆固醇水平的失调可能会引发神经退行性疾病,如阿尔茨海默病、帕金森病和亨廷顿病。我们之前曾报道过,通过降低与β-淀粉样蛋白(Aβ)产生密切相关的磷脂酰肌醇 4,5-二磷酸(PIP)水平,增加膜胆固醇水平可调节离子通道。此外,胆固醇富集通过增加培养细胞中磷脂酶 C(PLC)β1 同工型的表达来降低 PIP 水平。在这项研究中,我们研究了高胆固醇饮食对大鼠大脑中磷脂酶 C(PLCβ1)表达和 PIP 水平的影响。高胆固醇饮食组大鼠大脑皮层中的 PIP 水平降低。PLCβ1 表达水平与 PIP 水平相关。然而,胆固醇和 PIP 水平之间没有相关性,这表明 PIP 水平通过大脑中的 PLCβ1 表达受胆固醇调节。因此,胆固醇和 PIP 之间存在相互作用,可能有助于神经退行性疾病的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b2c/7038105/55a9d517f143/ijms-21-01161-g001.jpg

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