Prenylated quinolinecarboxylic acid derivative suppresses immune response through inhibition of PAK2

Biochem Pharmacol. 2016 Apr 1:105:55-65. doi: 10.1016/j.bcp.2016.01.020. Epub 2016 Jan 28.

Abstract

Development of new immunosuppressing agents is necessary in organ transplantation or immune diseases. Because Ppc-1 exhibits a suppressing effect on interleukin-2 (IL2) production in Jurkat cells, we synthesized and screened Ppc-1 derivatives that preserve prenylated quinolinecarboxylic acid (PQA) structure, and identified compound 18 (PQA-18) as a novel molecule with immunosuppressing effect. PQA-18 suppressed not only IL2 but also IL4, IL6, and tumor necrosis factor-α production in human peripheral lymphocytes without affecting cell viability. Two-dimensional gel electrophoresis analysis and in vitro kinase assay revealed that PQA-18 inhibits kinase activity of p21-activated kinase 2 (PAK2). Administration of PQA-18 by intraperitoneal injection suppressed the population of a subset of regulatory T cells and the immunoglobulin (Ig) production against T cell-dependent antigens in mice. Treatment with the PQA-18 ointment on Nc/Nga mice, a model of human atopic dermatitis, improved skin lesions and serum IgE levels. These results suggest that PQA-18 is a unique PAK2 inhibitor with potent immunosuppressing effects in vitro and in vivo. PQA-18 may be a valuable lead for the development of novel immunosuppressants.

Keywords: Cytokine; Dermatitis; Immune response; Immunosuppressant; PQA-18 (PubChem CID: 73602831); Ppc-1 (PubChem CID: 46910769); Small molecule.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carboxylic Acids / chemistry
  • Carboxylic Acids / pharmacology*
  • Dermatitis / drug therapy
  • Dermatitis / immunology
  • Dermatitis / metabolism
  • Dose-Response Relationship, Drug
  • Humans
  • Immunity, Cellular / drug effects
  • Immunity, Cellular / immunology
  • Immunity, Cellular / physiology*
  • Immunosuppressive Agents / pharmacology*
  • Jurkat Cells
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Prenylation / drug effects
  • Prenylation / immunology
  • Prenylation / physiology*
  • Quinolines / chemistry
  • Quinolines / pharmacology*
  • T-Lymphocytes, Regulatory / drug effects
  • T-Lymphocytes, Regulatory / immunology
  • T-Lymphocytes, Regulatory / metabolism
  • Triiodobenzoic Acids / pharmacology
  • p21-Activated Kinases / antagonists & inhibitors
  • p21-Activated Kinases / immunology
  • p21-Activated Kinases / metabolism*

Substances

  • Carboxylic Acids
  • Immunosuppressive Agents
  • Quinolines
  • Triiodobenzoic Acids
  • compound 18
  • Pak2 protein, mouse
  • p21-Activated Kinases