Effect of Regulation of Chemerin/Chemokine-like Receptor 1/Stimulator of Interferon Genes Pathway on Astrocyte Recruitment to Aβ Plaques

• Published in: International journal of molecular sciences Vol. 25; no. 8; p. 4324
• Main Authors: Liu, Zhen, Chen, Yijun, Chen, Yanqing, Zheng, Jiayi, Wu, Wanning, Wang, Linlin, Wang, Hanqi, Yu, Yang
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.04.2024
• Subjects: Advertising executives; Alzheimer Disease - genetics; Alzheimer Disease - metabolism; Alzheimer Disease - pathology; Alzheimer's disease; Amyloid beta-Peptides - metabolism; Animals; astrocyte; Astrocytes - metabolism; Biological response modifiers; Brain research; Cell Movement; chemerin; Chemokines; Chemokines - metabolism; chemR23; CMKLR1; Drug approval; Genes; Genotype & phenotype; Humans; Intercellular Signaling Peptides and Proteins - genetics; Intercellular Signaling Peptides and Proteins - metabolism; Interferon; Ligands; Localization; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, Transgenic; migration; Nervous system diseases; Neurons; Pathology; Plaque, Amyloid - metabolism; Plaque, Amyloid - pathology; Receptors, Chemokine - genetics; Receptors, Chemokine - metabolism; Signal Transduction; Transgenic animals; Tumor necrosis factor-TNF; China; Aβ; Alzheimer’s disease; chemR23; migration; STING; chemerin; astrocyte; CMKLR1
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25084324

Recruitment and accumulation of reactive astrocytes around senile plaques are common pathological features of Alzheimer's disease (AD), with unclear mechanisms. Chemerin, an adipokine implicated in neuroinflammation, acts through its receptor, chemokine-like receptor 1 (CMKLR1), which also functions as a receptor for amyloid β (Aβ). The impact of the chemerin/CMKLR1 axis on astrocyte migration towards Aβ plaques is unknown. Here we investigated the effect of CMKLR1 on astrocyte migration around Aβ deposition in APP/PS1 mice with knockout (APP/PS1- ). CMKLR1-expressed astrocytes were upregulated in the cortices and hippocampi of 9-month-old APP/PS1 mice. Chemerin mainly co-localized with neurons, and its expression was reduced in the brains of APP/PS1 mice, compared to WT mice. CMKLR1 deficiency decreased astrocyte colocalization with Aβ plaques in APP/PS1- mice, compared to APP/PS1 mice. Activation of the chemerin/CMKLR1 axis promoted the migration of primary cultured astrocytes and U251 cells, and reduced astrocyte clustering induced by Aβ . Mechanistic studies revealed that chemerin/CMKLR1 activation induced STING phosphorylation. Deletion of STING attenuated the promotion of the chemerin/CMKLR1 axis relative to astrocyte migration and abolished the inhibitory effect of chemerin on Aβ -induced astrocyte clustering. These findings suggest the involvement of the chemerin/CMKLR1/STING pathway in the regulation of astrocyte migration and recruitment to Aβ plaques/Aβ .