1 Peripheral blood lymphocytes express dopamine D-1-like and D-2-like receptors which were investigated using radioligand binding assay and molecular biology techniques. Analysis of dopamine D-2-like receptors expressed by human peripheral blood lymphocytes with radioligand binding assay may offer a rapid technique for assessing receptor changes in disorders characterized by involvement of the dopaminergic system. However, the suitability of radioligand binding assay techniques to measure dopamine D-2-like receptors is questioned. 2 In view of the discrepancy between data of dopamine D-2-like receptor determination with molecular biology and radioligand binding assay techniques, we have assayed dopamine D-2-like receptors expressed by human peripheral blood lymphocytes using as radioligands the dopamine receptor agonist 7-[H-3]-hydroxy-N,N-di-n-propyl-2-aminotetraline ([H-3]-7-OH-DPAT) and two antagonists ([H-3]-spiperone and [H-3]-nemonapride). 3 Analysis of saturation curves revealed a concentration-dependent binding of all compounds to human peripheral blood lymphocytes. Dissociation constant (K-d) values averaged between 0.15 and 0.40 nM for different radioligands. The maximum density of binding sites (B-max) was low, ranging from 4.15 +/- 0.05 fmol/10(6) cells with [H-3]-spiperone and 8.66 +/- 0.04 fmol/10(6) cells with [H-3]-7-OH-DPAT. 4 Displacement curves of [H-3]-7-OH-DPAT, [H-3]-spiperone and [H-3]-nemonapride binding to human peripheral blood lymphocytes revealed, using radioligand concentrations giving the highest specific:non-specific binding ratio, a pharmacological profile consistent with the labelling of dopamine D-2-like receptors. The use of higher radioligand concentrations resulted in a poorly displaceable and characterizable binding. 5 Detection of dopamine D-2, D-3 and D-4 receptor immunoreactivity in cytospin centrifuged peripheral blood lymphocytes revealed dopamine D-3 and D-4 but not D-2 receptor immunostaining. 6 The above findings indicate in agreement with molecular biology studies, that dopamine D-2-like receptors expressed by human peripheral blood lymphocytes belong to the D-3 and D-4 receptor subtypes. These receptors are detectable using either dopamine D-2-like receptor agonists and antagonists as radioligands if controlled experimental conditions are followed. The standardisation of immunocytochemical techniques for detecting human peripheral blood lymphocyte dopamine receptors may contribute to clarify their role in lymphocyte function or as a peripheral marker of the status of the dopaminergic system.