Thrombopoietin stimulates megakaryocytopoiesis, myelopoiesis, and expansion of CD34+ progenitor cells from single CD34+ Thy-1+ Lin-primitive progenitor cells

JC Young, E Bruno, KM Luens, S Wu, M Backer… - 1996 - ashpublications.org
JC Young, E Bruno, KM Luens, S Wu, M Backer, LJ Murray
1996ashpublications.org
Thrombopoietin (TPO) or MpI ligand is known to stimulate megakaryocyte (MK) proliferation
and differentiation. To identify the earliest human hematopoietic cells on which TPO acts, we
cultured single CD34+ Thy-1+ Lin-adult bone marrow cells in the presence of TPO alone,
with TPO and interleukin-3 (IL-3), or with TPO and c-kit ligand (KL) in the presence of a
murine stromal cell line (Sys1). Two distinct growth morphologies were observed: expansion
of up to 200 blast cells with subsequent differentiation to large refractile CD41b+ MKs within …
Abstract
Thrombopoietin (TPO) or MpI ligand is known to stimulate megakaryocyte (MK) proliferation and differentiation. To identify the earliest human hematopoietic cells on which TPO acts, we cultured single CD34+Thy- 1+Lin- adult bone marrow cells in the presence of TPO alone, with TPO and interleukin-3 (IL-3), or with TPO and c-kit ligand (KL) in the presence of a murine stromal cell line (Sys1). Two distinct growth morphologies were observed: expansion of up to 200 blast cells with subsequent differentiation to large refractile CD41b+ MKs within 3 weeks or expansion to 200–10,000 blast cells, up to 25% of which expressed CD34. The latter blast cell expansions occurred over a 3- to 6-week period without obvious MK differentiation. Morphological staining, analysis of surface marker expression, and colony formation analysis revealed that these populations consisted predominantly of cells committed to the myelomonocytic lineage. The addition of IL-3 to TPO-containing cultures increased the extent of proliferation of single cells, whereas addition of KL increased the percentage of CD34+ cells among the expanding cell populations. Production of multiple colony- forming unit-MK from single CD34+Thy-1+Lin- cells in the presence of TPO was also demonstrated. In limiting dilution assays of CD34+Lin- cells, TPO was found to increase the size and frequency of cobblestone areas at 4 weeks in stromal cultures in the presence of leukemia inhibitory factor and IL-6. In stroma-free cultures, TPO activated a quiescent CD34+Lin-Rhodamine 123lo subset of primitive hematopoietic progenitor cells into cycle, without loss of CD34 expression. These data demonstrate that TPO acts directly on and supports division of cells more primitive than those committed to the MK lineage.
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