Increased expression of CX43 on stromal cells promotes leukemia apoptosis

Oncotarget. 2015 Dec 29;6(42):44323-31. doi: 10.18632/oncotarget.6249.

Abstract

Connexin 43 (Cx43) induced apoptosis has been reported in solid tumors, but the effect of Cx43 expressed by bone marrow stromal cells (BMSC) in leukemia has not been fully investigated. Manipulating Cx43 expression could be a potential therapeutic strategy for leukemia. Here, we investigate the effect of Cx43 expressed by BMSCs (human Umbilical Cord Stem Cells over-expressed CX43, Cx43-hUCSC) on leukemia cells. When co-cultured with Cx43-hUCSC, leukemia cells show significant lower growth rate with increasing apoptosis activity, and more leukemia cells enter S phase. Functional assays of fluorescence recovery after photo bleaching (FRAP) showed improved gap junctional intercellular communication (GJIC) on leukemia cells when co-cultured with Cx43-hUCSC (p < 0.01). In a mouse minimal disease model, the mean survival time and mortality rate were significantly improved in mice transplanted with Cx43-hUCSC. Our results indicate that Cx43 expressed by BMSC induces apoptosis on leukemia cells. Small molecules or other pharmaceutical approaches for modulating Cx43 expression in BMSCs could be used for delaying relapse of leukemia.

Keywords: apoptosis; bone marrow stromal cells; leukemia.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis*
  • Caspases / metabolism
  • Cell Cycle Checkpoints
  • Cell Proliferation
  • Cells, Cultured
  • Coculture Techniques
  • Connexin 43 / genetics
  • Connexin 43 / metabolism*
  • Cord Blood Stem Cell Transplantation
  • Enzyme Activation
  • Female
  • Fetal Blood / cytology
  • Gap Junctions / metabolism
  • Humans
  • Leukemia / metabolism*
  • Leukemia / pathology
  • Leukemia / surgery
  • Mesenchymal Stem Cells / metabolism*
  • Mice
  • Neoplasms, Experimental / metabolism*
  • Neoplasms, Experimental / pathology
  • Neoplasms, Experimental / surgery
  • Paracrine Communication*
  • Recurrence
  • Time Factors
  • Transfection
  • Up-Regulation

Substances

  • Connexin 43
  • GJA1 protein, human
  • Caspases