Nerve growth factor enhances the CRE-dependent transcriptional activity activated by nobiletin in PC12 cells

Author:

Takito Jiro1,Kimura Junko2,Kajima Koji3,Uozumi Nobuyuki4,Watanabe Makoto5,Yokosuka Akihito6,Mimaki Yoshihiro6,Nakamura Masanori1,Ohizumi Yasushi25

Affiliation:

1. Department of Oral Anatomy and Developmental Biology, School of Dentistry, Showa University, 1-5-8 Hatanodai, Shinagawa, Tokyo 142-8555, Japan.

2. Department of Medical Biochemistry, School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka, Japan.

3. Sankyo Holdings Co., Ltd., 573-13 Denbou, Fuji-shi, Shizuoka, Japan.

4. Department of Biomolecular Engineering, Graduate School of Engineering, Tohoku University, 6-6-07 Aobayama, Sendai, Miyagi, Japan.

5. Kansei Fukushi Research Center, Tohoku Fukushi University, 6-149-1 Kunimigaoka, Aoba-ku, Sendai, Miyagi, Japan.

6. Laboratory of Medicinal Plant Science, School of Pharmacy, Tokyo University of Pharmacy and Life Science, 1432-1 Horinouchi, Hachioji, Tokyo, Japan.

Abstract

Prevention and treatment of Alzheimer disease are urgent problems for elderly people in developed countries. We previously reported that nobiletin, a poly-methoxylated flavone from the citrus peel, improved the symptoms in various types of animal models of memory loss and activated the cAMP responsive element (CRE)-dependent transcription in PC12 cells. Nobiletin activated the cAMP/PKA/MEK/Erk/MAPK signaling pathway without using the TrkA signaling activated by nerve growth factor (NGF). Here, we examined the effect of combination of nobiletin and NGF on the CRE-dependent transcription in PC12 cells. Although NGF alone had little effect on the CRE-dependent transcription, NGF markedly enhanced the CRE-dependent transcription induced by nobiletin. The NGF-induced enhancement was neutralized by a TrkA antagonist, K252a. This effect of NGF was effective on the early signaling event elicited by nobiletin. These results suggested that there was crosstalk between NGF and nobiletin signaling in activating the CRE-dependent transcription in PC12 cells.

Publisher

Canadian Science Publishing

Subject

Physiology (medical),Pharmacology,General Medicine,Physiology

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