Investigating the effects of taurine on Aβ-degradation proteins and neurogenesis-related genes in an LPS-induced neuroinflammatory SH-SY۵Y cell model
محل انتشار: مجله علوم پایه پزشکی ایران، دوره: 29، شماره: 7
سال انتشار: 1405
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 116
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شناسه ملی سند علمی:
JR_IJBMS-29-7_007
تاریخ نمایه سازی: 1 تیر 1405
چکیده مقاله:
Objective(s): Taurine, a brain-abundant sulfonic acid, shows potential neuroprotective effects and may counter neurodegenerative processes. This study investigated the effects of taurine on neuroinflammation, focusing on Aβ-degrading proteins and gene expression related to neurogenesis in an LPS-stimulated SH-SY۵Y cell model.Materials and Methods: The effects of taurine (۰.۵ and ۱ mg/ml) and LPS (۰.۵ and ۱۰ μg/ml) on SH-SY۵Y cell viability were assessed using the MTT assay. IL-۱β and IL-۶ expression was measured by real-time PCR, while matrix metalloproteinases (MMPs) and angiotensin-converting enzyme (ACE) levels were quantified via ELISA. Neurogenesis-related gene expression was evaluated using the Neurogenesis Plus RT² Profiler PCR array.Results: The MTT assay results demonstrated that taurine treatment at concentrations of ۰.۵ and ۱ mg/ml significantly attenuated the cytotoxicity induced by LPS stimulation in SH-SY۵Y cells. Also, treatment with taurine significantly reduced the expression levels of the inflammatory genes IL-۱β and IL-۶ in LPS-stimulated SH-SY۵Y cells (P<۰.۰۵). ELISA results further revealed that taurine treatment significantly increased the secretion levels of ACE and MMP-۹ enzymes in LPS-stimulated SH-SY۵Y cells (P<۰.۰۵). LPS exposure in SH-SY۵Y cells significantly up-regulated genes related to apoptosis, cell migration, and synaptic function (P<۰.۰۰۵). Conversely, taurine treatment significantly increased the expression of genes involved in cell adhesion, synaptic function, growth factors, cytokines, differentiation, cell cycle, signaling, transcription, and cofactor activity (P<۰.۰۰۵).Conclusion: These results suggest that taurine may act as a potential neuroprotective agent by increasing the secretion of MMP-۹ and ACE, regulating neurogenesis-related genes, and reducing LPS-induced neuroinflammation.
کلیدواژه ها:
Lipopolysaccharides ، Matrix metalloproteinase ۹ ، Neurogenesis Neuroinflammatory - diseases ، Neuroprotective agents Taurine
نویسندگان
Pirouz Pourmohammad
Department of Biochemistry, North Tehran Branch, Islamic Azad University, Tehran, Iran
Fereshteh Rahmati
Department of Biochemistry, North Tehran Branch, Islamic Azad University, Tehran, Iran
Fatemeh Siadat
Department of Biochemistry, North Tehran Branch, Islamic Azad University, Tehran, Iran
Sara Simorgh
Department of Tissue Engineering & Regenerative Medicine, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran
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