Aim. To determine the role of sodium caseinate (CasNa) in the modulation of
hemopoiesis. Materials and methods. 32D cells, a murine hemopoietic multip
otential cell line dependent on interleukin-3 (IL-3) for proliferation and
survival, were used. These cells were cultured with 0.5 ng/mL of IL-3, toge
ther with different concentrations of CasNa. We evaluated: proliferation (d
irect counting under the microscope and use of thymidine H-3), morphologica
l differentiation (giemsa staining), cytochemistry (specific staining for m
onocytes and granulocytes), and function (presence of Fc receptors and redu
ction of nitro-blue tetrazolium). In addition, we determined cell viability
through trypan blue exclusion and apoptosis using the TUNEL assay in situ.
Results. We showed that CasNa induced a decrease in cell proliferation, wh
ich is dose dependent, and is neither a result of a diminished cell viabili
ty, nor due to an increase in cell death through apoptosis. In addition, Ca
sNa induces cell differentiation towards the monocytic lineage. Conclusions
. CasNa has the capacity to differentiate 32D cells towards the monocytic l
ineage, and, importantly, has a potent differentiating activity on 32D cell
s being able to promote differentiation in a shorter time than the well Kno
wn factors G-CSF and GM-CSF.