We recently demonstrated the expression of somatostatin (SS) and SS receptor (SSR) subtype 1 (sst₁), sst_2A and sst₃ in normal human thymic tissue and of sst₁ and sst_2A on isolated thymic epithelial cells (TEC). We also found an inhibitory effect of SS and octreotide on TEC proliferation. In the current study we further investigated the presence and function of SSR in freshly purified human thymocytes at various stages of development. Thymocytes represent a heterogeneous population of lymphoid cells displaying different levels of maturation and characterized by specific cell surface markers. In the this study, we firstly demonstrated specific high affinity [¹²⁵I-Tyr¹¹]-SS-14 binding on thymocyte membrane homogenates. Subsequently, by RT-PCR, sst_2A and sst₃ mRNA expression was detected in the whole thymocyte population. After separation of thymocytes into subpopulations, we found by quantitative RT-PCR that sst_2A and sst₃ are differentially expressed in intermediate/mature and immature thymocytes. The expression of sst₃ mRNA was higher in the intermediate/mature CD3⁺ fraction compared with the immature CD2⁺CD3^- one, while sst_2A mRNA was less abundant in the intermediate/mature CD3⁺ thymocytes. In 7 days cultured thymocytes SSR subtype mRNA expression was lost. SS-14 significantly inhibited ³H-Thymidine incorporation in all thymocyte cultures, indicating the presence of functional receptors. Conversely, octreotide significantly inhibited ³H-Thymidine incorporation only in the cultures of immature CD2⁺CD3^- thymocyte. Sst₃ is mainly expressed on intermediate/mature thymocyte fraction and most of these cells generally die by apoptosis. Since SS-14, but not octreotide,induced a significant increase in the percent of apoptotic thymocytes, it might be that sst₃ is involved in this process. Moreover, sst₃ has been recently demonstrated on peripheral human T lymphocytes, which directly derive from mature thymocytes, and SS analogs may induce apoptosis in these cells. Interestingly, CD14⁺ thymic cells, which are cells belonging to the monocytes-macrophage lineage, selectively expressed sst_2A mRNA. Finally, SSR expression in human thymocytes seems to follow a developmental pathway. The heterogeneous expression of SSR within the human thymus on specific cell subsets and the endogenous production of SS as well as SS-like peptides emphasize their role in the bi-directional interactions between the main cell components of the thymus involved in intrathymic T-cell maturation.