[Transforming growth factor-β1 induces bone marrow-derived mesenchymal stem cells to differentiate into cancer-associated fibroblasts]

Zhonghua Zhong Liu Za Zhi. 2015 Nov;37(11):804-9.
[Article in Chinese]

Abstract

Objective: To investigate the effect of transforming growth factor-β1 (TGF-β1) on the differentiation of bone marrow-derived mesenchymal stem cells (MSCs) into cancer-associated fibroblasts(CAFs).

Methods: MSCs were cultured in α-MEM with recombinant human TGF-β1 or in tumor-conditioned medium.The expression of CAFs markers were detected by immunofluorescence and quantitative RT-PCR.

Results: The qRT-PCR assay showed that the expression of CAFs markers FAP, ACTA, CAV, CCL5, CXCR4, FSP1, SDF-1 and vimentin were 9.92±2.16, 7.76±1.28, 3.04±0.95, 3.28±2.16, 2.13±0.71, 1.41±0.66, 2.25±0.86 and 1.38±0.56, respectively, significantly upregulated in the MSCs co-cultured with TGF-β1 or TCM. The relative levels of FAP, ACTA, CAV, CCL5, CXCR4, FSP1, SDF-1 and vimentin mRNA in the TCM group were 7.52±1.76, 5.02±1.18, 1.98±1.19, 1.82±1.19, 2.95±0.86, 1.44±0.67, 2.08±0.74 and 1.47±0.55, respectively, indicating that MSCs can express CAFs phenotype.TGF beta signaling pathway inhibitor SB-431542 could inhibit the differentiation. Both immunofluorescence and Western blot confirmed the above results.

Conclusions: TGF-β1 induces differentiation of local MSCs to CAFs by upregulating the expression of pSmad3, so as to further promote the growth of cancer cells.

MeSH terms

  • Benzamides / pharmacology
  • Bone Marrow Cells / cytology
  • Cell Differentiation / drug effects*
  • Cell Line, Tumor
  • Chemokine CXCL12 / metabolism
  • Coculture Techniques
  • Culture Media, Conditioned
  • Dioxoles / pharmacology
  • Fibroblasts / cytology*
  • Humans
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / drug effects*
  • Organic Chemicals
  • Receptors, CXCR4 / metabolism
  • Recombinant Proteins / pharmacology
  • Smad3 Protein / metabolism
  • Transforming Growth Factor beta1 / antagonists & inhibitors
  • Transforming Growth Factor beta1 / pharmacology*
  • Vimentin / metabolism

Substances

  • 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide
  • Benzamides
  • CXCL12 protein, human
  • Chemokine CXCL12
  • Culture Media, Conditioned
  • Dioxoles
  • Organic Chemicals
  • Receptors, CXCR4
  • Recombinant Proteins
  • SMAD3 protein, human
  • Smad3 Protein
  • Transforming Growth Factor beta1
  • Vimentin
  • alpha minimal essential medium