Phosphorylation of c-Cbl and p85 PI3K driven by all-trans retinoic acid and CD38 depends on Lyn kinase activity

Cell Signal. 2014 Jul;26(7):1589-97. doi: 10.1016/j.cellsig.2014.03.021. Epub 2014 Mar 29.

Abstract

The leukocyte antigen CD38 is expressed after all-trans retinoic acid (ATRA) treatment in HL-60 myelogenous leukemia cells and promotes induced myeloid differentiation when overexpressed. We found that Vav1 and SLP-76 associate with CD38 in two cell lines, and that these proteins complex with Lyn, a Src family kinase (SFK) upregulated by ATRA. SFK inhibitors PP2 and dasatinib, which enhance ATRA-induced differentiation, were used to evaluate the involvement of Lyn kinase activity in CD38-driven signaling. Cells treated with ATRA for 48h followed by one hour of PP2 incubation show SFK/Lyn kinase inhibition. We observed that Lyn inhibition blocked c-Cbl and p85/p55 PI3K phosphorylation driven by the anti-CD38 agonistic mAb IB4 in ATRA-treated HL-60 cells and untreated CD38+ transfectants. In contrast, cells cultured for 48h following concurrent ATRA and PP2 treatment did not show Lyn inhibition, suggesting ATRA regulates the effects on Lyn. 48h of co-treatment preserved CD38-stimulated c-Cbl and p85/p55 PI3K phosphorylation indicating Lyn kinase activity is necessary for these events. In contrast another SFK inhibitor (dasatinib) which blocks Lyn activity with ATRA co-treatment prevented ATRA-induced c-Cbl phosphorylation and crippled p85 PI3K phosphorylation, indicating Lyn kinase activity is important for ATRA-propelled events potentially regulated by CD38. We found that loss of Lyn activity coincided with a decrease in Vav1/Lyn/CD38 and SLP-76/Lyn/CD38 interaction, suggesting these molecules form a complex that regulates CD38 signaling. Lyn inhibition also reduced Lyn and CD38 binding to p85 PI3K, indicating CD38 facilitates a complex responsible for PI3K phosphorylation. Therefore, Lyn kinase activity is important for CD38-associated signaling that may drive ATRA-induced differentiation.

Keywords: All-trans retinoic acid; CD38 signaling; Lyn; Src family kinases.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADP-ribosyl Cyclase 1 / biosynthesis
  • ADP-ribosyl Cyclase 1 / metabolism*
  • Adaptor Proteins, Signal Transducing / biosynthesis
  • Adaptor Proteins, Signal Transducing / metabolism
  • Antineoplastic Agents / pharmacology
  • Cell Differentiation / drug effects
  • Cell Line, Tumor
  • Class Ia Phosphatidylinositol 3-Kinase / metabolism*
  • Dasatinib
  • HL-60 Cells
  • Humans
  • Leukemia, Myeloid / drug therapy
  • Membrane Glycoproteins / biosynthesis
  • Membrane Glycoproteins / metabolism*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphoproteins / biosynthesis
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Protein Binding / drug effects
  • Protein Kinase Inhibitors / pharmacology
  • Proto-Oncogene Proteins c-cbl / metabolism
  • Proto-Oncogene Proteins c-vav / biosynthesis
  • Proto-Oncogene Proteins c-vav / metabolism
  • Pyrimidines / pharmacology
  • Thiazoles / pharmacology
  • Tretinoin / pharmacology*
  • src-Family Kinases / antagonists & inhibitors
  • src-Family Kinases / metabolism*

Substances

  • AG 1879
  • Adaptor Proteins, Signal Transducing
  • Antineoplastic Agents
  • Membrane Glycoproteins
  • Phosphoproteins
  • Protein Kinase Inhibitors
  • Proto-Oncogene Proteins c-vav
  • Pyrimidines
  • SLP-76 signal Transducing adaptor proteins
  • Thiazoles
  • VAV1 protein, human
  • Tretinoin
  • Proto-Oncogene Proteins c-cbl
  • Phosphatidylinositol 3-Kinases
  • Class Ia Phosphatidylinositol 3-Kinase
  • PIK3R3 protein, human
  • lyn protein-tyrosine kinase
  • src-Family Kinases
  • CD38 protein, human
  • ADP-ribosyl Cyclase 1
  • CBL protein, human
  • Dasatinib