Protective effects of microRNA‐330 on amyloid β‐protein production, oxidative stress, and mitochondrial dysfunction in Alzheimer's disease by targeting VAV1 via the MAPK signaling pathway

• Published in: Journal of cellular biochemistry Vol. 119; no. 7; pp. 5437 - 5448
• Main Authors: Zhou, Ying, Wang, Zhou‐Fan, Li, Wei, Hong, Hui, Chen, Juan, Tian, Yi, Liu, Zhao‐Yun
• Format: Journal Article
• Language: English
• Published: United States 01.07.2018
• Subjects: Alzheimer's disease; microRNA‐330; mitogen‐activated protein kinase signaling pathway; oxidative stress; VAV1; microRNA-330; mitogen-activated protein kinase signaling pathway; Alzheimer's disease; VAV1; oxidative stress
• ISSN: 0730-2312; 1097-4644
• DOI: 10.1002/jcb.26700

This study aims to explore the effect of miR‐330 targeting VAV1 on amyloid β‐protein (Aβ) production, oxidative stress (OS), and mitochondrial dysfunction in Alzheimer's disease (AD) mice through the MAPK signaling pathway. Putative targeted gene of miR‐330 was performed by a miRNA target prediction website and dual‐luciferase reporter gene assay. AD mouse model was successfully established. Fourteen C57 mice were randomized into AD and control groups. The positive protein expression rate of VAV1 was measured by immunohistochemistry. Neuron cells were assigned into control, blank, negative control (NC), miR‐330 mimics, miR‐330 inhibitors, siRNA‐VAV1, and miR‐330 inhibitors + siRNA‐VAV1 groups. Expression of miR‐330, VAV1, ERK1, JNK1, P38MAPK, Aβ, COX, and lipoprotein receptor‐related protein‐1 (LRP‐1) were determined using RT‐qPCR and Western blotting. Colorimetry was applied to measure the levels of OS parameters of superoxide dismutase (SOD) and malondialdehyde (MDA). Aβ production in brain tissue was detected using ELISA, while that in neuron cell was measured by radioimmunoassay. MiR‐330 was down‐regulated in neuron cells of AD mice and VAV1 was negatively regulated by miR‐330. Compared with the control group, the positive protein expression rate of VAV1 was significantly elevated in the AD group. Overexpression of miR‐330 decreased the expression of VAV1, ERK1, JNK1, P38MAPK, and Aβ, but increased the expression of COX and LRP‐1. AD mice revealed elevated Aβ production and MDA with decreased SOD level. The result indicates that overexpressed miR‐330 targeting VAV1 through the MAPK signaling pathway reduces Aβ production and alleviates OS and mitochondrial dysfunction in AD. The result indicates that overexpressed miR‐330 targeting VAV1 through the MAPK signaling pathway reduces Aβ production and alleviates oxidative stress and mitochondrial dysfunction in AD mice.