We examined the role of the ligand forc‐mpl, thrombopoietin (TPO), in murine early haemopoiesis, using a serum‐free culture system. TPO in combination with the ligand forc‐kit(SF) or interleukin‐3 (IL‐3) supported colony formation by marrow cells of 5‐fluorouracil (5‐FU)‐treated mice, whereas TPO alone yielded no colony. When blast cell colonies grown in the presence of TPO plus SF or TPO plus IL‐3 were individually replated in suspension cultures containing serum and several growth factors, various combinations of myeloid lineages were seen, indicating that the progenitors supported by TPO plus SF or TPO plus IL‐3 are multipotential. Delayed addition experiments demonstrated that TPO has the potential to effectively support the survival of haemopoietic progenitors. We then studied the effects of TPO on proliferative kinetics of cycling progenitors. TPO hastened IL‐3‐dependent growth of progenitors by shortening the time required for cell cycling. These results suggest that TPO, as a single factor, can support the survival of haemopoietic progenitors and TPO synergizes with SF or IL‐3 to act on early multipotential
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