Fig. 5.
(A) Expression of both isoforms of OB-R in two patients newly diagnosed with APL and one patient with recurrent APL compared with expression in normal bone marrow (NBM), FACS-sorted normal myeloid progenitors, peripheral blood (PB), and MO7E cells (as positive control). In one APL sample (lane 3) OB-R expression was detected in peripheral blood containing 37% promyelocytes. (B) OB-R expression of FACS-sorted CD34+33− and CD34−33+ APL cells in complete remission (CR). OB-R was identified only in the CD34+compartment of NBM. In contrast, in a sample from a patient with newly diagnosed APL containing 90% promyelocytes and no CD34+cells, the level of OB-R expression corresponded to that seen in NBM, which was used as a control.

(A) Expression of both isoforms of OB-R in two patients newly diagnosed with APL and one patient with recurrent APL compared with expression in normal bone marrow (NBM), FACS-sorted normal myeloid progenitors, peripheral blood (PB), and MO7E cells (as positive control). In one APL sample (lane 3) OB-R expression was detected in peripheral blood containing 37% promyelocytes. (B) OB-R expression of FACS-sorted CD34+33 and CD3433+ APL cells in complete remission (CR). OB-R was identified only in the CD34+compartment of NBM. In contrast, in a sample from a patient with newly diagnosed APL containing 90% promyelocytes and no CD34+cells, the level of OB-R expression corresponded to that seen in NBM, which was used as a control.

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