Transferrin receptor expression on AML blasts is related to their proliferative potential

Publisher Website
Google Scholar
Abstract
Summary. Expression of the transferrin receptor (TfR) was studied on peripheral blood blast cells from 11 patients with acute myeloid leukaemia (AML). Using a monoclonal anti‐TfR antibody (OKT9) and a polyclonal antibody against surface membrane‐bound transferrin, a proportion of blasts from all the patients was found to express receptors for transferrin. Further analysis of OKT9 expression using a fluorescent activated cell sorter (FACS) showed that the TfR was heterogeneously distributed in the blast cell population. In five out of six samples studied, stimulation of DNA synthesis following short‐term culture induced a several‐fold increase in TfR display as analysed by flow cytometry using OKT9 or FITC‐conjugated transferrin. Blasts from seven patients stained with OKT9 were separated on the FACS into positive and negative or weakly positive fractions. Culture of the TfR negative population in a blast cell colony assay produced no colonies in either of two patients. In a further five patients the colony forming cells were predominately associated with the TfR strongly positive fraction (52 ± 25 colonies/104 cells) rather than the TfR weakly positive fraction (12 ± 11 colonies/104 cells). Analysis of colony size showed that clones derived from the weakly positive fraction were smaller than clones from the TfR strongly positive fraction. These results suggest that TfR display by AML blasts is related to their proliferative capacity and is expressed by the leukaemic stem cell fraction.