IGF-1 promotes the development and cytotoxic activity of human NK cells

Nat Commun. 2013:4:1479. doi: 10.1038/ncomms2484.

Abstract

Insulin-like growth factor 1 (IGF-1) is a critical regulator of many physiological functions, ranging from longevity to immunity. However, little is known about the role of IGF-1 in natural killer cell development and function. Here, we identify an essential role for IGF-1 in the positive regulation of human natural killer cell development and cytotoxicity. Specifically, we show that human natural killer cells have the ability to produce IGF-1 and that differential endogenous IGF-1 expression leads to disparate cytotoxicity in human primary natural killer cells. Moreover, miR-483-3p is identified as a critical regulator of IGF-1 expression in natural killer cells. Overexpression of miR-483-3p has an effect similar to IGF-1 blockade and decreased natural killer cell cytotoxicity, whereas inhibition of miR-483-3p has the opposite effect, which is reversible with IGF-1 neutralizing antibody. These findings indicate that IGF-1 and miR-483-3p belong to a new class of natural killer cell functional modulators and strengthen the prominent role of IGF-1 in innate immunity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions / genetics
  • Antigens, CD34 / metabolism
  • Base Sequence
  • Cell Count
  • Cell Differentiation / drug effects
  • Cell Differentiation / immunology
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Cytotoxicity, Immunologic / drug effects*
  • Fetal Blood / cytology
  • Flow Cytometry
  • Gene Expression Regulation / drug effects
  • Gene Knockdown Techniques
  • Humans
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor I / metabolism
  • Insulin-Like Growth Factor I / pharmacology*
  • Killer Cells, Natural / cytology*
  • Killer Cells, Natural / drug effects
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / metabolism
  • Lymphocyte Subsets / cytology
  • Lymphocyte Subsets / drug effects
  • Lymphocyte Subsets / metabolism
  • MicroRNAs / metabolism
  • Molecular Sequence Data
  • Protein Binding / drug effects
  • Protein Binding / genetics
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Subcellular Fractions / drug effects
  • Subcellular Fractions / metabolism

Substances

  • 3' Untranslated Regions
  • Antigens, CD34
  • MIRN483 microRNA, human
  • MicroRNAs
  • RNA, Messenger
  • Insulin-Like Growth Factor I