1.AKAP12 regulates vascular integrity in zebrafish.
Hyouk Bum KWON ; Yoon Kyung CHOI ; Jhong Jae LIM ; Seung Hae KWON ; Song HER ; Hyun Jin KIM ; Kyung Joon LIM ; Jong Chan AHN ; Young Myeong KIM ; Moon Kyung BAE ; Jeong Ae PARK ; Chul Ho JEONG ; Naoki MOCHIZUKI ; Kyu Won KIM
Experimental & Molecular Medicine 2012;44(3):225-235
The integrity of blood vessels controls vascular permeability and extravasation of blood cells, across the endothelium. Thus, the impairment of endothelial integrity leads to hemorrhage, edema, and inflammatory infiltration. However, the molecular mechanism underlying vascular integrity has not been fully understood. Here, we demonstrate an essential role for A-kinase anchoring protein 12 (AKAP12) in the maintenance of endothelial integrity during vascular development. Zebrafish embryos depleted of akap12 (akap12 morphants) exhibited severe hemorrhages. In vivo time-lapse analyses suggested that disorganized interendothelial cell-cell adhesions in akap12 morphants might be the cause of hemorrhage. To clarify the molecular mechanism by which the cell-cell adhesions are impaired, we examined the cell-cell adhesion molecules and their regulators using cultured endothelial cells. The expression of PAK2, an actin cytoskeletal regulator, and AF6, a connector of intercellular adhesion molecules and actin cytoskeleton, was reduced in AKAP12-depleted cells. Depletion of either PAK2 or AF6 phenocopied AKAP12-depleted cells, suggesting the reduction of PAK2 and AF6 results in the loosening of intercellular junctions. Consistent with this, overexpression of PAK2 and AF6 rescued the abnormal hemorrhage in akap12 morphants. We conclude that AKAP12 is essential for integrity of endothelium by maintaining the expression of PAK2 and AF6 during vascular development.
A Kinase Anchor Proteins/*genetics/metabolism
;
Animals
;
Blood Vessels/abnormalities/*embryology/metabolism
;
Cell Cycle Proteins/genetics/metabolism
;
Down-Regulation
;
Embryo, Nonmammalian/abnormalities/*blood supply/embryology/metabolism
;
Gene Deletion
;
*Gene Expression Regulation, Developmental
;
Hemorrhage/*embryology/genetics/metabolism
;
Human Umbilical Vein Endothelial Cells
;
Humans
;
Intercellular Junctions/genetics/metabolism/ultrastructure
;
Kinesin/genetics/metabolism
;
Myosins/genetics/metabolism
;
Zebrafish/*embryology/genetics
;
p21-Activated Kinases/genetics/metabolism