High glucose increase cell cycle regulatory proteins level of mouse embryonic stem cells via PI3-K/Akt and MAPKs signal pathways

✍ Scribed by Yun Hee Kim; Jung Sun Heo; Ho Jae Han

• Publisher: John Wiley and Sons
• Year: 2006
• Tongue: English
• Weight: 408 KB
• Volume: 209
• Category: Article
• ISSN: 0021-9541
• DOI: 10.1002/jcp.20706

✦ Synopsis

Abstract

This study examined the effects of high glucose on cell proliferation and its related signal pathways using mouse embryonic stem (ES) cells. Here, we showed that high glucose level significantly increased [^3^H]thymidine incorporation, BrdU incorporation, the number of cells, [^3^H]leucine, and [^3^H]proline incorporation in a time‐(>3 hr) and dose‐(>25 mM) dependent manner. Moreover, high glucose level increased the cellular reactive oxygen species (ROS), Akt, and mitogen‐activated protein kinases (MAPKs) phosphorylation. Subsequently, these signaling molecules involved in high glucose‐induced increase of [^3^H]thymidine incorporation. High glucose level also increased cyclin D1, cyclin E, cyclin‐dependent kinase (CDK) 2, and CDK 4 protein levels, which is cell cycle regulatory proteins acting in G1–S phase of cell cycle. Inhibition of phosphatidylinositol 3‐kinase (PI3‐K) (LY 294002: PI3‐kinase inhibitor, 10^−6^ M), Akt (Akt inhibitor, 10^−5^ M), and p44/42 MAPKs (PD 98059: MEK inhibitor, 10^−5^ M) decreased these proteins. High glucose level phosphorylated the RB protein, which was decreased by inhibition of PI3‐K and Akt. In conclusion, high glucose level stimulates mouse ES cell proliferation via the PI3‐K/Akt and MAPKs pathways. J. Cell. Physiol. 209: 94–102, 2006. © 2006 Wiley‐Liss, Inc.