An analog of a dipeptide-like structure of FK506 increases glial cell line-derived neurotrophic factor expression through cAMP response element-binding protein activated by heat shock protein 90/Akt signaling pathway

被引:37
作者
Cen, XB
Nitta, A
Ohya, S
Zhao, YL
Ozawa, N
Mouri, A
Ibi, D
Wang, L
Suzuki, M
Saito, K
Ito, Y
Kawagoe, T
Noda, Y
Ito, Y
Furukawa, S
Nabeshima, T [1 ]
机构
[1] Nagoya Univ, Grad Sch Med, Dept Neuropsychopharmacol & Hosp Pharm, Showa Ku, Nagoya, Aichi 4668560, Japan
[2] Sichuan Univ, Nat Chengdu Ctr Safety Evaluat Tradit Chinese Med, W China Hosp, Chengdu 610041, Peoples R China
[3] Gifu Univ, Sch Med, Dept Lab Med, Gifu 5008705, Japan
[4] Nagoya Univ, Equipment Ctr Res & Educ, Grad Sch Med, Nagoya, Aichi 4668560, Japan
[5] Dept Res & Dev, Tokyo 1070062, Japan
[6] Meijo Univ, Fac Pharm, Div Clin Sci Clin Pharm Practice Management & Res, Nagoya, Aichi 4688503, Japan
[7] Nihon Univ, Dept Pharmacol, Coll Pharm, Chiba 2748555, Japan
[8] Gifu Pharmaceut Univ, Mol Biol Lab, Gifu 5028585, Japan
关键词
GDNF; dipeptide; FK506; Hsp90; Hsc70; CREB;
D O I
10.1523/JNEUROSCI.5010-05.2006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Glial cell line-derived neurotrophic factor ( GDNF) is an important neurotrophic factor that has therapeutic implications for neurodegenerative disorders. We previously showed that leucine-isoleucine (Leu-Ile), an analog of a dipeptide-like structure of FK506 ( tacrolimus), induces GDNF expression both in vivo and in vitro. In this investigation, we sought to clarify the cellular mechanisms underlying the GDNF-inducing effect of this dipeptide. Leu-Ile transport was investigated using fluorescein isothiocyanate-Leu-Ile in cultured neurons, and the results showed the transmembrane mobility of this dipeptide. By liquid chromatography-mass spectrometry and quartz crystal microbalance assay, we identified heat shock cognate protein 70 as a protein binding specifically to Leu-Ile, and molecular modeling showed that the ATPase domain is the predicted binding site. Leu-Ile stimulated Akt phosphorylation, which was attenuated significantly by heat shock protein 90 (Hsp90) inhibitor geldanamycin (GA). Moreover, enhanced interaction between phosphorylated Akt and Hsp90 was detected by immunoprecipitation. Leu-Ile elicited an increase in cAMP response element binding protein ( CREB) phosphorylation, which was inhibited by GA, indicating that CREB is a downstream target of Hsp90/Akt signaling. Leu-Ile elevated the levels of GDNF mRNA and protein expression, whereas inhibition of CREB blocked such effects. Leu-Ile promoted the binding activity of phosphorylated CREB with cAMP response element. These findings show that CREB plays a key role in transcriptional regulation of GDNF expression induced by Leu-Ile. In conclusion, Leu-Ile activates Hsp90/Akt/CREB signaling, which contributes to the upregulation of GDNF expression. It may represent a novel lead compound for the treatment of dopaminergic neurons or motoneuron diseases.
引用
收藏
页码:3335 / 3344
页数:10
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