In order to define a cellular model suitable for studying, in vitro, the mo
lecular properties and functions of neurotrophin receptors in human lymphoc
ytes, TrkA, TrkB, TrkC and p75(NTR) expression was investigated in a panel
of EBV immortalized lymphoblastoid (LCL) and Burkitt lymphoma-derived cell
lines (BLs) compared to primary B lymphocytes by RT-PCR and flow cytometric
analysis, Our data show that trkA and trkB are transcribed in most B cell
lines of normal and malignant origin, For several of them, we also gained f
irst evidence of trkC expression in B cells. All cell lines and primary B c
ells lack p75(NTR) expression. These data suggest that neurotrophin recepto
rs expression in the B cell lines correlates to some extent with the phenot
ypic maturation stage and endogenous viral activity levels, Our data sugges
t that TrkA and TrkB, once activated, provide a partial rescue from apoptos
is, whereas TrkC stimulates the progression through the cell cycle without
affecting cell survival. Finally, the identification of a number of cell li
nes showing single expression of one of the Trk receptors has disclosed the
availability of a cellular tool for further studies on their function, and
mechanisms of signal transduction in the B cell moiety in the absence of p
75(NTR).