In:
Molecular Biology of the Cell, American Society for Cell Biology (ASCB), Vol. 20, No. 6 ( 2009-03-15), p. 1695-1704
Abstract:
Extracellular calcium (Cao) is a major regulator of keratinocyte differentiation, but the mechanism is unclear. Phosphatidylinositol-4-phosphate 5-kinase 1α (PIP5K1α) is critical in synthesizing phosphatidylinositol 4,5-bisphosphate [PI(4,5)P 2 ]. In this study, we sought to determine whether PIP5K1α plays a role in mediating the ability of Cao to induce keratinocyte differentiation. We found that treatment of human keratinocytes in culture with Cao resulted in increased PIP5K1α level and activity, as well as PI(4,5)P 2 level, binding of phosphatidylinositol 3,4,5-triphosphate [PI(3,4,5)P 3 ] to and activation of phospholipase C-γ1 (PLC-γ1), with the resultant increase in inositol 1,4,5-trisphosphate (IP 3 ) and intracellular calcium (Cai). Knockdown of PIP5K1α in human keratinocytes blocked Cao-induced increases in the binding of PI(3,4,5)P 3 to PLC-γ1; PLC-γ1 activity; levels of PI(4,5)P 2 , IP 3 , and Cai; and induction of keratinocyte differentiation markers. Coimmunoprecipitation and confocal studies revealed that Cao stimulated PIP5K1α recruitment to the E-cadherin–catenin complex in the plasma membrane. Knockdown of E-cadherin or β-catenin blocked Cao-induced activation of PIP5K1α. These results indicate that after Cao stimulation PIP5K1α is recruited by the E-cadherin–catenin complex to the plasma membrane where it provides the substrate PI(4,5)P 2 for both PI3K and PLC-γ1. This signaling pathway is critical for Cao-induced generation of the second messengers IP 3 and Cai and keratinocyte differentiation.
Type of Medium:
Online Resource
ISSN:
1059-1524
,
1939-4586
DOI:
10.1091/mbc.e08-07-0756
Language:
English
Publisher:
American Society for Cell Biology (ASCB)
Publication Date:
2009
detail.hit.zdb_id:
1474922-1
SSG:
12
