SSeCKS promoted lipopolysaccharide-sensitized astrocytes migration via increasing β-1,4-galactosyltransferase-I activity

• Published in: Neurochemical research 2019-04, Vol.44 (4), p.839-848
• Main Authors: Wei, Hua, Xu, Leiting, Li, Chunmiao, Liu, Lianliang, Ng, Derry Minyao, Haleem, Maria, Jiang, Lingli, Sun, Ning, Ling, Qingzhi, Ma, Shaohua, Zhang, Lingli, Wang, Qinwen, Tao, Tao
• Format: Article
• Language: English
• Subjects: A Kinase Anchor Proteins - metabolism; Animals; Animals, Newborn; Astrocytes; Astrocytes - drug effects; Astrocytes - metabolism; Biochemistry; Biomedical and Life Sciences; Biomedicine; Cell adhesion & migration; Cell Biology; Cell Cycle Proteins - metabolism; Cell migration; Cell Movement - drug effects; Cell Movement - physiology; Cells, Cultured; Central nervous system; Enzyme Activation - drug effects; Enzyme Activation - physiology; Extracellular matrix; Galactosyltransferases - metabolism; Glycoproteins; Golgi apparatus; Immunofluorescence; Inflammation; Inflammatory response; Lipopolysaccharides; Lipopolysaccharides - pharmacology; Neurochemistry; Neurology; Neurosciences; Original Paper; Proteins; Rats; Rats, Sprague-Dawley; Receptors; Substrates; Wound healing
• ISSN: 0364-3190; 1573-6903
• DOI: 10.1007/s11064-019-02716-5

Astrocytes migration is essential in the formation of the glial scar during the injury response process of the central nervous system (CNS) especially during inflammation. Integrin β1 is part of the extracellular matrix receptors in the CNS and it has been reported that integrin β-deficient astrocytes randomly migrate into wounds. Previous studies have found that β-1,4 Galactosyltransferase-I (β-1,4-GalT-I) enhanced the β-1,4-galactosylation of integrin β1. Src-suppressed C kinase substrate (SSeCKS) is an inflammatory response protein which functionally interacts with β-1,4 Galactosyltransferase-I (β-1,4-GalT-I). In this study we aim to investigate the role of SSeCKS and β-1,4-GalT-I in the migration of astrocytes during lipopolysaccharide (LPS)-induced inflammation. Coimmunoprecipitation and immunofluorescence assays have demonstrated that SSeCKS and β-1,4-GalT-I were significantly enhanced in LPS-treated astrocytes and their interactions may occur in the Trans-Golgi Network. Lectin blot showed that the knockdown of β-1,4-GalT-I could inhibit the β-1,4-galactosylation of glycoproteins including integrin β1 with and without LPS, and that SSeCKS knockdown inhibits the β-1,4-galactosylation of glycoproteins including integrin β1 only in LPS-induced astrocytes. Additionally, wound healing assays indicated that β-1,4-GalT-I knockdown could inhibit astrocytes migration with and without LPS but SSeCKS inhibited cell migration only when LPS was present. Therefore our findings suggest that SSeCKS affects astrocytes migration by regulating the β-1,4-galactosylation of glycoproteins including integrin β1, via β-1,4-GalT-I expression in LPS-sensitized astrocytes.