Effects of the gp130 cytokines ciliary neurotropic factor (CNTF) and interleukin-11 on pituitary cells: CNTF receptors on human pituitary adenomas and stimulation of prolactin and GH secretion in normal rat anterior pituitary aggregate cultures

J Endocrinol. 2001 Jun;169(3):539-47. doi: 10.1677/joe.0.1690539.

Abstract

Two of the most potent cytokines regulating anterior pituitary cell function are leukemia inhibitory factor (LIF) and interleukin (IL)-6, which belong to the cytokine family using the common gp130 signal transducer. Recently, the expression and action of two other members of this family, IL-11 and ciliary neurotrophic factor (CNTF), on different cell lines has also been demonstrated. We studied the expression of the specific receptor subunits for CNTF in mammotropic, non-functioning and somatotropic tumors and the action of CNTF and IL-11 in the regulation of hormone secretion in these and normal pituitary cells. The mRNA for the alpha chain specific for the CNTF receptor was detected by Northern blot in tumors secreting prolactin (PRL) and GH and in non-functioning tumors. We found that both IL-11 and CNTF exerted a similar stimulatory effect on GH mRNA expression in somatotropic monolayer cell cultures from acromegalic tumors, but these cytokines had no significant influence on GH secretion. CNTF stimulates prolactin secretion in lactotropic monolayer cell cultures from patients with prolactinoma. In monolayer cell cultures from normal rat anterior pituitary, IL-11 and CNTF had no significant effect on the release of either GH or PRL, or on GH mRNA. However, when the cells were cultured in aggregate cultures, in which the three-dimensional structure of the cells is reconstituted, both cytokines, in doses at which they had no effect on monolayer cultures, significantly stimulated both PRL and GH secretion. These data show that IL-11 and CNTF may act as regulatory factors in anterior pituitary cells, in which the three-dimensional structure of the gland is of critical importance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoma / metabolism*
  • Animals
  • Cell Aggregation
  • Cell Culture Techniques
  • Ciliary Neurotrophic Factor / pharmacology*
  • Gene Expression Regulation, Neoplastic / drug effects
  • Human Growth Hormone / biosynthesis
  • Human Growth Hormone / genetics
  • Humans
  • Interleukin-11 / pharmacology*
  • Male
  • Neoplasm Proteins / metabolism
  • Pituitary Gland, Anterior / cytology
  • Pituitary Gland, Anterior / drug effects*
  • Pituitary Neoplasms / metabolism*
  • Prolactin / metabolism
  • RNA, Messenger / genetics
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Ciliary Neurotrophic Factor / metabolism
  • Tumor Cells, Cultured

Substances

  • Ciliary Neurotrophic Factor
  • Interleukin-11
  • Neoplasm Proteins
  • RNA, Messenger
  • Receptor, Ciliary Neurotrophic Factor
  • Human Growth Hormone
  • Prolactin