P2X1 Receptor-Mediated Ca2+ Influx Triggered by DA-9801 Potentiates Nerve Growth Factor-Induced Neurite Outgrowth

Moon Jung Back, Hae Kyung Lee, Joo Hyun Lee, Zhicheng Fu, Mi Won Son, Sang Zin Choi, Hyo Sang Go, Sungjae Yoo, Sun Wook Hwang, Dae Kyong Kim

Research output: Contribution to journalArticle

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Abstract

Nerve growth factor (NGF)-induced neuronal regeneration has emerged as a strategy to treat neuronal degeneration-associated disorders. However, direct NGF administration is limited by the occurrence of adverse effects at high doses of NGF. Therefore, development of a therapeutic strategy to promote the NGF trophic effect is required. In view of the lack of understanding of the mechanism for potentiating the NGF effect, this study investigated molecular targets of DA-9801, a well-standardized Dioscorea rhizome extract, which has a promoting effect on NGF. An increase in intracellular calcium ion level was induced by DA-9801, and chelation of extracellular calcium ions with ethylene-bis(oxyethylenenitrilo)tetraacetic acid (EGTA) suppressed the potentiating effect of DA-9801 on NGF-induced neurite outgrowth. In addition, EGTA treatment reduced the DA-9801-induced phosphorylation of extracellular signal-regulated kinase1/2 (ERK1/2), the major mediators of neurite outgrowth. To find which calcium ion-permeable channel contributes to the calcium ion influx induced by DA-9801, we treated PC12 cells with various inhibitors of calcium ion-permeable channels. NF449, a P2X1 receptor selective antagonist, significantly abolished the potentiating effect of DA-9801 on NGF-induced neurite outgrowth and abrogated the DA-9801-induced ERK1/2 phosphorylation. In addition, transfection with siRNA of P2X1 receptor significantly reduced the DA-9801-enhanced neurite outgrowth. In conclusion, calcium ion influx through P2X1 receptor mediated the promoting effect of DA-9801 on NGF-induced neurite outgrowth via ERK1/2 phosphorylation.

Original languageEnglish
Pages (from-to)1488-1498
Number of pages11
JournalACS Chemical Neuroscience
Volume7
Issue number11
DOIs
Publication statusPublished - 2016 Nov 16

Fingerprint

Purinergic P2X1 Receptors
Nerve Growth Factor
Ions
Calcium
Phosphorylation
Egtazic Acid
Calcium Channels
Dioscorea
DA-9801
Neuronal Outgrowth
Rhizome
PC12 Cells
Chelation
Small Interfering RNA
Transfection
Regeneration

Keywords

  • calcium ion influx
  • DA-9801
  • neurite outgrowth
  • P2X1

ASJC Scopus subject areas

  • Physiology
  • Biochemistry
  • Cognitive Neuroscience
  • Cell Biology

Cite this

P2X1 Receptor-Mediated Ca2+ Influx Triggered by DA-9801 Potentiates Nerve Growth Factor-Induced Neurite Outgrowth. / Back, Moon Jung; Lee, Hae Kyung; Lee, Joo Hyun; Fu, Zhicheng; Son, Mi Won; Choi, Sang Zin; Go, Hyo Sang; Yoo, Sungjae; Hwang, Sun Wook; Kim, Dae Kyong.

In: ACS Chemical Neuroscience, Vol. 7, No. 11, 16.11.2016, p. 1488-1498.

Research output: Contribution to journalArticle

Back, Moon Jung ; Lee, Hae Kyung ; Lee, Joo Hyun ; Fu, Zhicheng ; Son, Mi Won ; Choi, Sang Zin ; Go, Hyo Sang ; Yoo, Sungjae ; Hwang, Sun Wook ; Kim, Dae Kyong. / P2X1 Receptor-Mediated Ca2+ Influx Triggered by DA-9801 Potentiates Nerve Growth Factor-Induced Neurite Outgrowth. In: ACS Chemical Neuroscience. 2016 ; Vol. 7, No. 11. pp. 1488-1498.
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abstract = "Nerve growth factor (NGF)-induced neuronal regeneration has emerged as a strategy to treat neuronal degeneration-associated disorders. However, direct NGF administration is limited by the occurrence of adverse effects at high doses of NGF. Therefore, development of a therapeutic strategy to promote the NGF trophic effect is required. In view of the lack of understanding of the mechanism for potentiating the NGF effect, this study investigated molecular targets of DA-9801, a well-standardized Dioscorea rhizome extract, which has a promoting effect on NGF. An increase in intracellular calcium ion level was induced by DA-9801, and chelation of extracellular calcium ions with ethylene-bis(oxyethylenenitrilo)tetraacetic acid (EGTA) suppressed the potentiating effect of DA-9801 on NGF-induced neurite outgrowth. In addition, EGTA treatment reduced the DA-9801-induced phosphorylation of extracellular signal-regulated kinase1/2 (ERK1/2), the major mediators of neurite outgrowth. To find which calcium ion-permeable channel contributes to the calcium ion influx induced by DA-9801, we treated PC12 cells with various inhibitors of calcium ion-permeable channels. NF449, a P2X1 receptor selective antagonist, significantly abolished the potentiating effect of DA-9801 on NGF-induced neurite outgrowth and abrogated the DA-9801-induced ERK1/2 phosphorylation. In addition, transfection with siRNA of P2X1 receptor significantly reduced the DA-9801-enhanced neurite outgrowth. In conclusion, calcium ion influx through P2X1 receptor mediated the promoting effect of DA-9801 on NGF-induced neurite outgrowth via ERK1/2 phosphorylation.",
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AU - Fu, Zhicheng

AU - Son, Mi Won

AU - Choi, Sang Zin

AU - Go, Hyo Sang

AU - Yoo, Sungjae

AU - Hwang, Sun Wook

AU - Kim, Dae Kyong

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