Leu27IGF2 plays an opposite role to IGF1 to induce H9c2 cardiomyoblast cell apoptosis via Gaq signaling

Ray Jade Chen, His Chin Wu, Mu Hsin Chang, Chao Hung Lai, Yun Chen Tien, Jin Ming Hwang, Wu Hsien Kuo, Fuu Jen Tsai, Chang Hai Tsai, Li Mien Chen, Chih Yang Huang, Chun Hsien Chu

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

This study examines the role of IGF2/mannose 6-phosphate receptor (IGF2R) signaling in the signaling transduction regulation and cell apoptosis in H9c2 cardiomyoblast cells. However, it is difficult to recognize the distinct activation of IGF2 signaling without interfacing with IGFI receptor (IGF1R) after exposure to IGF2. Leu27IGF2, an analog of IGF2 that interacts selectively with the IGF2R, was used to specifically activate IGF2R signaling in this study. DNA fragmentation and TUNEL assay revealed that in contrast to IGF1 treatment preventing angiotensin II and AG1024-induced cell apoptosis, Leu27IGF2 appears to synergistically increase apoptosis in those cells. We further found cell apoptosis induction and an increase in the active form of caspase 3 in the treatment of cells with Leu27IGF2, but not IGF1. To detect the interaction between IGF2R and Gaq using the immunoprecipitation assay, we found that IGF2R could directly interact with Gaq and after treatment with Leu27IGF2 the binding ability of Gaq to IGF2R had increased. This sequentially resulted in the phosphorylation of phospholipase C-b, a key downstream modulator of Gaq, on serine 537. Moreover, disruption of the Gaq protein by small interferon RNA reduced the cell apoptosis induced by Leu27IGF2. Our findings demonstrate that IGF2R activation appears to induce cell apoptosis via Gaq-deriving signaling cascades and its effect is completely different from IGF1R survival signaling.

Original languageEnglish
Pages (from-to)221-230
Number of pages10
JournalJournal of Molecular Endocrinology
Volume43
Issue number6
DOIs
Publication statusPublished - Dec 2009
Externally publishedYes

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IGF Type 2 Receptor
Apoptosis
In Situ Nick-End Labeling
Type C Phospholipases
DNA Fragmentation
Immunoprecipitation
Caspase 3
Angiotensin II
Serine
Interferons
Phosphorylation
RNA

ASJC Scopus subject areas

  • Endocrinology
  • Molecular Biology

Cite this

Leu27IGF2 plays an opposite role to IGF1 to induce H9c2 cardiomyoblast cell apoptosis via Gaq signaling. / Chen, Ray Jade; Wu, His Chin; Chang, Mu Hsin; Lai, Chao Hung; Tien, Yun Chen; Hwang, Jin Ming; Kuo, Wu Hsien; Tsai, Fuu Jen; Tsai, Chang Hai; Chen, Li Mien; Huang, Chih Yang; Chu, Chun Hsien.

In: Journal of Molecular Endocrinology, Vol. 43, No. 6, 12.2009, p. 221-230.

Research output: Contribution to journalArticle

Chen, RJ, Wu, HC, Chang, MH, Lai, CH, Tien, YC, Hwang, JM, Kuo, WH, Tsai, FJ, Tsai, CH, Chen, LM, Huang, CY & Chu, CH 2009, 'Leu27IGF2 plays an opposite role to IGF1 to induce H9c2 cardiomyoblast cell apoptosis via Gaq signaling', Journal of Molecular Endocrinology, vol. 43, no. 6, pp. 221-230. https://doi.org/10.1677/JME-08-0121
Chen, Ray Jade ; Wu, His Chin ; Chang, Mu Hsin ; Lai, Chao Hung ; Tien, Yun Chen ; Hwang, Jin Ming ; Kuo, Wu Hsien ; Tsai, Fuu Jen ; Tsai, Chang Hai ; Chen, Li Mien ; Huang, Chih Yang ; Chu, Chun Hsien. / Leu27IGF2 plays an opposite role to IGF1 to induce H9c2 cardiomyoblast cell apoptosis via Gaq signaling. In: Journal of Molecular Endocrinology. 2009 ; Vol. 43, No. 6. pp. 221-230.
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AU - Hwang, Jin Ming

AU - Kuo, Wu Hsien

AU - Tsai, Fuu Jen

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AU - Chen, Li Mien

AU - Huang, Chih Yang

AU - Chu, Chun Hsien

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