Journal
EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 668, Issue 1-2, Pages 42-56Publisher
ELSEVIER
DOI: 10.1016/j.ejphar.2011.06.026
Keywords
alpha(1)-Adrenoceptor; Mitogen-activated protein kinase; Akt; Induced pluripotent stem cell
Categories
Funding
- National Defense Medical College [23]
- Japan Society for the Promotion of Sciences [22500687]
- Smoking Research Foundation [33]
- Grants-in-Aid for Scientific Research [22500687] Funding Source: KAKEN
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Since the clinical use of induced pluripotent stem (iPS) cells may overcome the current obstacles in stem cell-based therapy, the molecular mechanisms that regulate iPS cell proliferation are of great interest. Therefore, in the present study, we determined the involvement of alpha(1)-adrenoceptor in the proliferation of mouse iPS cells. The selective alpha(1)-adrenoceptor agonist L-phenylephrine dose-dependently increased the proliferation of mouse iPS cells cultured in a medium with leukemia inhibitory factor (LIF). Pretreatment with either selective alpha(1)-adrenoceptor antagonists or protein kinase C (PKC) inhibitors significantly inhibited L-phenylephrine-induced DNA synthesis. The treatment with an IP3 receptor agonist significantly enhanced LIF-induced DNA synthesis. On the other hand, we confirmed that the intracellular calcium level was increased by the treatment with L-phenylephrine. Thus, intracellular calcium release or PKC activation induced by alpha(1)-adrenoceptor activation may lead to the enhancement of DNA synthesis. In addition, pretreatment with mitogen-activated protein kinase (MAPK) kinase (MEK) inhibitor PD98059 or phosphatidylinositol-3 phosphate kinase (PI3K) inhibitor LY294002 significantly inhibited L-phenylephrine-induced DNA synthesis. Treatment with L-phenylephrine significantly increased Akt or p44/42MAPK phosphorylation. alpha(1)-Adrenoceptor expression in mouse iPS cells was confirmed by immunofluorescence staining and western blotting analysis. In mouse iPS cells cultured with LIF, stimulation with L-phenylephrine significantly increased the proportion of cells in the S and G(2)/Mphases and decreased that in the G(1) phase. These results suggest that stimulation with alpha(1)-adrenoceptor may enhance DNA synthesis and proliferation of mouse iPS cells cultured with LIF via augmentation of both the MEK/MAPK and the PI3K/Akt pathways. (C) 2011 Elsevier B. V. All rights reserved.
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