TGF-beta utilizes SMAD3 to inhibit CD16-mediated IFN-gamma production and antibody-dependent cellular cytotoxicity in human NK cells

J Immunol. 2008 Sep 15;181(6):3784-92. doi: 10.4049/jimmunol.181.6.3784.

Abstract

TGF-beta can be a potent suppressor of lymphocyte effector cell functions and can mediate these effects via distinct molecular pathways. The role of TGF-beta in regulating CD16-mediated NK cell IFN-gamma production and antibody-dependent cellular cytotoxicity (ADCC) is unclear, as are the signaling pathways that may be utilized. Treatment of primary human NK cells with TGF-beta inhibited IFN-gamma production induced by CD16 activation with or without IL-12 or IL-2, and it did so without affecting the phosphorylation/activation of MAP kinases ERK and p38, as well as STAT4. TGF-beta treatment induced SMAD3 phosphorylation, and ectopic overexpression of SMAD3 resulted in a significant decrease in IFN-gamma gene expression following CD16 activation with or without IL-12 or IL-2. Likewise, NK cells obtained from smad3(-/-) mice produced more IFN-gamma in response to CD16 activation plus IL-12 when compared with NK cells obtained from wild-type mice. Coactivation of human NK cells via CD16 and IL-12 induced expression of T-BET, the positive regulator of IFN-gamma, and T-BET was suppressed by TGF-beta and by SMAD3 overexpression. An extended treatment of primary NK cells with TGF-beta was required to inhibit ADCC, and it did so by inhibiting granzyme A and granzyme B expression. This effect was accentuated in cells overexpressing SMAD3. Collectively, our results indicate that TGF-beta inhibits CD16-mediated human NK cell IFN-gamma production and ADCC, and these effects are mediated via SMAD3.

Publication types

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

MeSH terms

  • Animals
  • Antibody-Dependent Cell Cytotoxicity / immunology*
  • Cell Line
  • Cell Line, Tumor
  • Female
  • GPI-Linked Proteins
  • Gene Expression Regulation / immunology
  • Humans
  • Immune Tolerance* / genetics
  • Interferon-gamma / antagonists & inhibitors*
  • Interferon-gamma / biosynthesis
  • Interleukin-12 / physiology
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Receptors, IgG / antagonists & inhibitors
  • Receptors, IgG / physiology*
  • Smad3 Protein / biosynthesis
  • Smad3 Protein / deficiency
  • Smad3 Protein / genetics
  • Smad3 Protein / physiology*
  • Transforming Growth Factor beta / physiology*

Substances

  • FCGR3B protein, human
  • GPI-Linked Proteins
  • Receptors, IgG
  • SMAD3 protein, human
  • Smad3 Protein
  • Transforming Growth Factor beta
  • Interleukin-12
  • Interferon-gamma