No abstract

The components of the insulin-like growth factor (IGF) axis have been investigated in the normal human thymus. Using ribonuclease protection assays (RPA), IGF-II transcripts were detected in the normal human thymus. By reverse transcriptase polymerase chain reaction (RT-PCR) analyses, promoters P3 and P4 were found to be active in the transcription of IGF2 gene within human thymic epithelial cells (TEC). No IGF-II mRNA could be detected in human lymphoid Jurkat T cells with 30 cycles of RT-PCR. By Northern blot analyses, IGFBP-2 to -6 (but not IGFBP-1) were found to be expressed in TEC with a predominance of IGFBP-4. Interestingly, Jurkat T cells only express IGFBP-2 but at high levels. The type 1 IGF receptor was detected in Jurkat T cells but not in human TEC. The identification of the components of the IGF axis within separate compartments of the human thymus adds further evidence for a role of this axis in the control of T-cell development. The precise influence of thymic IGF axis upon T-cell differentiation and immunological self-tolerance however needs to be further investigated.

No abstract

Inhibin extracted from human seminal plasma and from rete testis fluid is a protein substance. Two forms of inhibin exist in RTF and each has a different molecular weight. The species of higher molecular weight systematically yields a product of lower molecular weight during chromatography. This phenomenon could represent depolymerization of the molecule, an associated transport protein or alternatively a precursor form of inhibin. The inhibin preparations utilized selectively lowered the levels of FSH as assessed both in vivo and in vitro. This action was not totally specific since increasing doses of inhibin also produced a lowering of the levels of LH. In contrast, these preparations did not influence the secretion of TSH, growth hormone or prolactin in vivo or in vitro. A direct effect of inhibin on pituitary cells has been clearly established by demonstrating a reduction in the release of FSH in response to GnRH and its synthesis in the pituitary cells. Additional direct effects on the hypothalamus and on gametogenesis in the testis remain to be excluded. On the basis of selective effects of inhibin on FSH secretion, one could envisage the utilization of this hormone as an antifertility agent.

Abstract. The effect of mouse epidermal growth factor (EGF) was investigated on DNA and protein synthesis, progesterone and inhibin production by bovine antral granulosa cells. When incubated for the whole period of culture, EGF inhibited inhibin production the second day of culture, progesterone the third and the fourth days whereas it stimulated DNA and protein synthesis only the fourth day of culture. Inhibition of progesterone and stimulation of DNA and protein were dose-dependent when treatment with EGF (pre-incubation) is followed by 24 h without EGF, a stimulatory effect on DNA and protein synthesis was observed after 48 and 72-h preincubation. Progesterone was reduced after 3 day preincubation and inhibin only after 2-day pre-incubation. Effects observed after 3-day pre-incubation were dosedependent. These experiments demonstrated the stimulatory effect of EGF on growth of granulosa cells and its inhibitory action on hormonal production by these cells in vitro. The inhibitory effect on progesterone and inhibin production is more precocious than stimulatory effect on DNA and protein synthesis. The inhibitory action of EGF on granulosa cell production of progesterone and inhibin could thus be not directly dependent on its stimulatory action on DNA synthesis.