Expression of the growth hormone/insulin-like growth factor axis during Balb/c thymus ontogeny and effects of growth hormone upon ex vivo T cell differentiation

Neuroimmunomodulation. 2012;19(3):137-47. doi: 10.1159/000328844. Epub 2012 Jan 18.

Abstract

Aims: We address the question of the expression and the role of the growth hormone/insulin-like growth factor (GH/IGF) axis in the thymus.

Methods: Using RT-qPCR, the expression profile of various components of the somatotrope GH/IGF axis was measured in different thymic cell types and during thymus embryogenesis in Balb/c mice. The effect of GH on T cell differentiation was explored via thymic organotypic culture.

Results: Transcription of Gh, Igf1, Igf2 and their related receptors predominantly occurred in thymic epithelial cells (TEC), while a low level of Gh and Igf1r transcription was also evidenced in thymic T cells (thymocytes). Gh, Ghr, Ins2, Igf1, Igf2, and Igfr1 displayed distinct expression profiles depending on the developmental stage. The protein concentrations of IGF-1 and IGF-2 were in accordance with the profile of their gene expression. In fetal thymus organ cultures (FTOC) derived from Balb/c mice, treatment with exogenous GH resulted in a significant increase of double negative CD4-CD8- T cells and CD4+ T cells, together with a decrease in double positive CD4+CD8+ T cells. These changes were inhibited by concomitant treatment with GH and the GH receptor (GHR) antagonist pegvisomant. However, GH treatment also induced a significant decrease in FTOC Gh, Ghr and Igf1 expression.

Conclusion: These data show that the thymotropic properties of the somatotrope GH/IGF-1 axis involve an interaction between exogenous GH and GHR expressed by TEC. Since thymic IGF-1 is not increased by GH treatment, the effects of GH upon T cell differentiation could implicate a different local growth factor or cytokine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / genetics
  • Cell Differentiation / immunology*
  • Cells, Cultured
  • Epithelial Cells / metabolism
  • Gene Expression / physiology
  • Growth Hormone / genetics
  • Growth Hormone / immunology
  • Growth Hormone / metabolism*
  • Insulin / genetics
  • Insulin / immunology
  • Insulin / metabolism
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor I / immunology
  • Insulin-Like Growth Factor I / metabolism*
  • Insulin-Like Growth Factor II / genetics
  • Insulin-Like Growth Factor II / immunology
  • Insulin-Like Growth Factor II / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Organ Culture Techniques
  • Real-Time Polymerase Chain Reaction
  • Receptor, IGF Type 1 / genetics
  • Receptor, IGF Type 1 / immunology
  • Receptor, IGF Type 1 / metabolism*
  • Receptors, Somatotropin / genetics
  • Receptors, Somatotropin / immunology
  • Receptors, Somatotropin / metabolism
  • T-Lymphocytes / cytology
  • T-Lymphocytes / metabolism
  • Thymocytes / metabolism
  • Thymus Gland / embryology
  • Thymus Gland / immunology*
  • Thymus Gland / metabolism

Substances

  • IGF2 protein, mouse
  • Ins2 protein, mouse
  • Insulin
  • Receptors, Somatotropin
  • insulin-like growth factor-1, mouse
  • Insulin-Like Growth Factor I
  • Insulin-Like Growth Factor II
  • Growth Hormone
  • Receptor, IGF Type 1