Interleukin-2 and phytohaemagglutinin stimulate the proliferation of tunicate cells.

Proliferative responses of cells in tunicate pharyngeal explants to human interleukins and mitogenic lectins were tested. Increased tritiated-thymidine [( 3H]-TdR) uptake was detected among pharyngeal cells incubated with recombinant human interleukin-2 (IL-2), and phytohaemagglutinin-P (PHA-P). Responses to IL-2 were dose-dependent and affected lymphocyte-like cells. Enhanced proliferation was stimulated by IL-2 in the absence of co-stimulants and was not synergized by co-incubation with human interleukin-1 (IL-1) or PHA-P. Anti-IL-2 polyclonal antibody inhibited the stimulatory activity of recombinant human interleukin-2 (rhIL-2). Of three lectins tested (concanavalin-A [Con-A], pokeweed mitogen [PWM] and PHA-P), only PHA-P proved to be mitogenic. Con-A and PWM did not significantly increase proliferative activity even though both lectins were capable of binding pharyngeal cells as revealed by flow cytometry and fluorescence microscopy. Similarly, human IL-1 had no effect on [3H]-TdR uptake either alone or in combination with IL-2 and PHA-P. These data suggest that the functions of some interleukin-like cytokines have been conserved during evolution.