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PMID: 18796006 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A food-derived synergist of NGF signaling: identification of protein tyrosine phosphatase 1B as a key regulator of NGF receptor-initiated signal transduction.

Journal of neurochemistry ·Vol. 107 ·No. 5 ·2008-12-00 ·Pages 1248-60

Shibata T, Nakahara H, Kita N, Matsubara Y, Han C, Morimitsu Y, Iwamoto N, Kumagai Y, Nishida M, Kurose H, Aoki N, Ojika M, Uchida K

Abstract

Neurotrophins, such as the nerve growth factor (NGF), play an essential role in the growth, development, survival and functional maintenance of neurons in the central and peripheral systems. They also prevent neuronal cell death under various stressful conditions, such as ischemia and neurodegenerative disorders. NGF induces cell differentiation and neurite outgrowth by binding with and activating the NGF receptor tyrosine kinase followed by activation of a variety of signaling cascades. We have investigated the NGF-dependent neuritogenesis enhancer potential of a food-derived small molecule contained in Brassica vegetables and identified the protein tyrosine phosphatase (PTP) 1B as a key regulator of the NGF receptor-initiated signal transduction. Based on an extensive screening of Brassica vegetable extracts for the neuritogenic-promoting activity in the rat pheochromocytoma cell line PC12, we found the Japanese horseradish, wasabi (Wasabia japonica, syn. Eutrema wasabi), as the richest source and identified 6-methylsulfinylhexyl isothiocyanate (6-HITC), an analogue of sulforaphane isolated from broccoli, as one of the major neuritogenic enhancers in the wasabi. 6-HITC strongly enhanced the neurite outgrowth and neurofilament expression elicited by a low-concentration of NGF that alone was insufficient to induce neuronal differentiation. 6-HITC also facilitated the sustained-phosphorylation of the extracellular signal-regulated kinase and the autophosphorylation of the NGF receptor TrkA. It was found that PTP1B act as a phosphatase capable of dephosphorylating Tyr-490 of TrkA and was inactivated by 6-HITC in a redox-dependent manner. The identification of PTP1B as a regulator of NGF signaling may provide new clues about the chemoprotective potential of food components, such as isothiocyanates.

MeSH Terms
Animals Biotinylation/methods Cysteine/metabolism Dose-Response Relationship, Drug Enzyme Inhibitors/pharmacology Flow Cytometry Green Fluorescent Proteins/biosynthesis,genetics Hydrogen Peroxide/pharmacology Isothiocyanates/pharmacology Mitogen-Activated Protein Kinase 3/metabolism Nerve Growth Factor/chemistry,pharmacology,physiology Neurites/drug effects,metabolism Oxidants/pharmacology PC12 Cells Phosphorylation/drug effects Protein Tyrosine Phosphatase, Non-Receptor Type 1/metabolism RNA, Small Interfering/genetics Rats Receptor, trkA/biosynthesis,genetics,physiology Signal Transduction/drug effects,physiology Transfection
Chemicals
6-methylsulfinylhexyl isothiocyanate Enzyme Inhibitors Isothiocyanates Oxidants RNA, Small Interfering Green Fluorescent Proteins Nerve Growth Factor Hydrogen Peroxide Receptor, trkA Mitogen-Activated Protein Kinase 3 Protein Tyrosine Phosphatase, Non-Receptor Type 1 Cysteine
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Shibata Takahiro
Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, Japan.
Nakahara Hiroko
Kita Narumi
Matsubara Yui
Han Chunguang
Morimitsu Yasujiro
Iwamoto Noriko
Kumagai Yoshito
Nishida Motohiro
Kurose Hitoshi
Aoki Naohito
Ojika Makoto
Uchida Koji
Article Info
Journal
Journal of neurochemistry
Abbr.
J Neurochem
ISSN
1471-4159
Published
2008-12-00
Epub
2008-00-24
Pages
1248-60
Language
English
Region
England
NLM ID
2985190R
Subset
IM
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