The signaling cascades of Ganoderma lucidum extracts in stimulating non-amyloidogenic protein secretion in human neuroblastoma SH-SY5Y cell lines

• Published in: Neuroscience letters 2008-12, Vol.448 (1), p.62-66
• Main Authors: Pinweha, Sirinthorn, Wanikiat, Payong, Sanvarinda, Yupin, Supavilai, Porntip
• Format: Article
• Language: English
• Subjects: Amyloid beta-Protein Precursor - metabolism; Amyloid precursor protein; Amyloid Precursor Protein Secretases - metabolism; Biological and medical sciences; Cell Line, Tumor; Complex Mixtures - pharmacology; Dose-Response Relationship, Drug; Enzyme Inhibitors - pharmacology; Extracellular Signal-Regulated MAP Kinases - metabolism; Fundamental and applied biological sciences. Psychology; Ganoderma lucidum; Humans; Mitogen activated protein kinase; Nerve growth factor; Neuroblastoma - metabolism; Phosphatidyl inositol 3-kinase; Phospholipase C; Protein kinase C; Protein Kinase C - metabolism; Reishi - chemistry; Signal Transduction - drug effects; Vertebrates: nervous system and sense organs
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/j.neulet.2008.10.028

Ganoderma lucidum (GL) is a medicinal mushroom that possesses various pharmacological properties which are also documented in the ancient reports where GL is praised for its effects on the promotion of health and longevity. In this study, we have investigated the effect of GL mycelia extracts on the non-amyloidogenic protein secretion (sAPPα) and the amyloid precursor protein (APP) expression in SH-SY5Y neuroblastoma cells. In order to characterize the signaling pathway which mediates GL-enhanced sAPPα secretion, we used inhibitors of nerve growth factor (NGF) signaling pathways, phosphatidylinositol 3 kinase (PI3K), phospholipase Cγ1 (PLCγ1), protein kinase C (PKC) and extracellular signal-regulated kinase (ERK1/2), to block GL-mediated sAPPα secretion as well as ERK1/2 and PKC activation by using Western blot analysis. Our results provided for the first time evidence that GL mycelia extracts increased APP expression and promoted sAPPα secretion. In addition, GL extracts activated ERK1/2 and PKC phosphorylation. The complex signaling cascades of PI3K and ERK may be responsible for GL-mediated sAPPα secretion.