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High glucose induced translocation of Aquaporin8 to chicken hepatocyte plasma membrane: Involvement of cAMP, PI3K/Akt, PKC, MAPKs, and microtubule

✍ Scribed by Han Na Suh; Sang Hun Lee; Min Young Lee; Jung Sun Heo; Yu Jin Lee; Ho Jae Han


Book ID
102301480
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
389 KB
Volume
103
Category
Article
ISSN
0730-2312

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✦ Synopsis


Abstract

Aquaporin8 (AQP8) is a transmembrane water channel that is found mainly in hepatocytes. The direct involvement of AQP8 in high glucose condition has not been established. Therefore, this study examined the effects of high glucose on AQP8 and its related signal pathways in primary cultured chicken hepatocytes. High glucose increased the movement of AQP8 from the intracellular membrane to plasma membrane in a 30 mM glucose concentration and in a time‐ (≥10 min) dependent manner. On the other hand, 30 mM mannitol did not affect the translocation of AQP8, which suggested the absence of osmotic effect. Thirty millimolar glucose increased intracellular cyclic adenosine 3, 5‐monophosphate (cAMP) level. Moreover, high glucose level induced Akt phosphorylation, protein kinase C (PKC) activation, p44/42 mitogen‐activated protein kinases (MAPKs), p38 MAPK, and c‐jun NH~2~‐terminal kinase (JNK) phosphorylation. On the other hand, inhibition of each pathway by SQ 22536 (adenylate cyclase inhibitor), LY 294002 (PI3‐K phosphatidylinositol 3‐kinase inhibitor), Akt inhibitor, staurosporine (PKC inhibitor), PD 98059 (MEK inhibitor), SB 203580 (p38 MAPK inhibitor), or SP 600125 (JNK inhibitor) blocked 30 mM glucose‐induced AQP8 translocation, respectively. In addition, inhibition of microtubule movement with nocodazole blocked high glucose‐induced AQP8 translocation. High glucose level also increased the level of kinesin light chain and dynein protein expression. In conclusion, high glucose level stimulates AQP8 via cAMP, PI3‐K/Akt, PKC, and MAPKs pathways in primary cultured chicken hepatocytes. J. Cell. Biochem. 103: 1089–1100, 2008. © 2007 Wiley‐Liss, Inc.