Reduction in Renal Ischemia-Reperfusion Injury in Mice by a Phosphoinositide 3-Kinase p110gamma-Specific Inhibitor

Transplantation. 2015 Oct;99(10):2070-6. doi: 10.1097/TP.0000000000000742.

Abstract

Background: Although renal ischemia-reperfusion injury (IRI) can cause delayed graft function, a targeted therapy is not yet available. Because phosphoinositide 3-kinases (PI3K) p110γ and p110δ play important roles in immune cell migration and function, we investigated the effects of PI3K p110γ- and p110δ-specific inhibitors in a murine renal IRI model.

Methods: Renal function was assessed by serum creatine and hematoxylin-eosin staining. Immune cell migration was assessed by flow cytometry and an in vitro cell migration assay using Transwell plates. Gene expression analysis and a multiplex cytokine/chemokine assay were performed to find cytokines/chemokines whose expression was upregulated in renal IRI and affected by p110γ-specific inhibitor.

Results: The PI3K p110γ-specific inhibitor, but not p110δ-specific inhibitor, significantly reduced serum creatine levels and acute tubular necrosis. These were accompanied by reduced infiltration of B cells and reduced expression of CXCL9, a CXCR3 ligand, suggesting that p110γ plays an important role in B-cell migration toward injured kidneys. An in vitro cell migration assay revealed for the first time that B-cell migration to injured kidney cells and to CXCL9 requires p110γ.

Conclusions: p110γ-specific inhibitor ameliorates renal IRI by reducing necrosis and immune cell migration. This inhibitor may have the potential to reduce renal graft failure caused by renal IRI.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Movement
  • Chemokine CXCL9 / metabolism
  • Class I Phosphatidylinositol 3-Kinases
  • Class Ib Phosphatidylinositol 3-Kinase / metabolism*
  • Creatine / blood
  • Enzyme Inhibitors / chemistry*
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Graft Survival
  • Kidney / pathology*
  • Kidney Tubular Necrosis, Acute / blood
  • Kidney Tubular Necrosis, Acute / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Necrosis
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Reperfusion Injury / pathology*

Substances

  • Chemokine CXCL9
  • Cxcl9 protein, mouse
  • Enzyme Inhibitors
  • Class I Phosphatidylinositol 3-Kinases
  • Class Ib Phosphatidylinositol 3-Kinase
  • Pik3cd protein, mouse
  • Pik3cg protein, mouse
  • Creatine