| First Author | Yoshioka W | Year | 2014 |
| Journal | Sci Rep | Volume | 4 |
| Pages | 4042 | PubMed ID | 24509627 |
| Mgi Jnum | J:210165 | Mgi Id | MGI:5569670 |
| Doi | 10.1038/srep04042 | Citation | Yoshioka W, et al. (2014) Predominant role of cytosolic phospholipase A2alpha in dioxin-induced neonatal hydronephrosis in mice. Sci Rep 4:4042 |
| abstractText | Hydronephrosis is a common disease characterized by dilation of the renal pelvis and calices, resulting in loss of kidney function in the most severe cases. 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) induces nonobstructive hydronephrosis in mouse neonates through upregulation of prostaglandin E2 (PGE2) synthesis pathway consisting of cyclooxygenase-2 (COX-2) and microsomal prostaglandin E synthase-1 (mPGES-1) by a yet unknown mechanism. We here studied possible involvement of cytosolic phospholipase A2alpha (cPLA2alpha) in this mechanism. To this end, we used a cPLA2alpha-null mouse model and found that cPLA2alpha has a significant role in the upregulation of the PGE2 synthesis pathway through a noncanonical pathway of aryl hydrocarbon receptor. This study is the first to demonstrate the predominant role of cPLA2alpha in hydronephrosis. Elucidation of the pathway leading to the onset of hydronephrosis using the TCDD-exposed mouse model will deepen our understanding of the molecular basis of nonobstructive hydronephrosis in humans. |
