Neuroendocrine-induced synthesis of bone marrow-derived cytokines with inflammatory immunomodulating properties


Whetsell M., Bagriacik E. Ü. , Seetharamaiah G., Prabhakar B., Klein J.

CELLULAR IMMUNOLOGY, vol.192, no.2, pp.159-166, 1999 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 192 Issue: 2
  • Publication Date: 1999
  • Doi Number: 10.1006/cimm.1998.1444
  • Journal Name: CELLULAR IMMUNOLOGY
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.159-166
  • Gazi University Affiliated: No

Abstract

Although cytokines and other soluble regulators of immunity are known to be involved in hematopoiesis, Little is known about the signals that induce the synthesis of those mediators locally. Based on recent studies linking the neuroendocrine hormone thyrotropin [thyroid-stimulating hormone (TSH)] to immune cell function in other tissues, we investigated the capacity of TSH to activate cytokine responses from bone marrow cells, These studies reveal that stimulation of the TSH receptor on bone marrow cells-using highly purified or recombinant TSH or by direct stimulation with anti-TSH receptor antibodies-rapidly induces the synthesis of cytokines from bone marrow cells that are classically used in the regulation of inflammatory responses. Of 13 cytokines screened for activity by ELISA or by RNase protection assays for gene expression, IL-6, IFN-beta, TNF alpha, TNF beta, TGF beta 2, and lymphotoxin-beta responses were reproducibly induced by TSH within 2-3 h of stimulation. Intracellularly, TSH stimulation of bone marrow cells caused rapid increases in cAMP levels and induced the phosphorylation of the Jak2 protein kinase, thereby defining a novel G-protein coupled receptor/cytokine synthesis pathway. These findings demonstrate that TSH can serve as a primary inductive signal of cytokine production by bone marrow cells. (C) 1999 Academic Press.