Polycythemia vera megakaryocytes but not megakaryocytes from normal controls and patients with smokers polyglobuly spontaneously express IL-6 and IL-6R and secrete IL-6

Citation
C. Wickenhauser et al., Polycythemia vera megakaryocytes but not megakaryocytes from normal controls and patients with smokers polyglobuly spontaneously express IL-6 and IL-6R and secrete IL-6, LEUKEMIA, 13(3), 1999, pp. 327-334
Citations number
40
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
LEUKEMIA
ISSN journal
08876924 → ACNP
Volume
13
Issue
3
Year of publication
1999
Pages
327 - 334
Database
ISI
SICI code
0887-6924(199903)13:3<327:PVMBNM>2.0.ZU;2-M
Abstract
Polycythemia rubra vera (PV) represents a clonal hematological disorder def ined by an abnormal expansion of erythroid precursors and megakaryopoiesis, in particular. Ample evidence has been provided that the IL-6/IL-6R comple x may be responsible for the proliferation of normal and neoplastic megakar yocytes in vitro and this fact lead us to the hypothesis, that defects in t he regulation of IL-6 synthesis take part in the pathogenesis of PV. The st udy was carried out to determine the IL-6 serum levels and the megakaryocyt ic IL-6 production in patients with PV and to compare these data with the s ituation in hematologically healthy donors as well as in patients suffering from spurious polycythemia - smokers polyglobuly (PG). For this purpose, I L-6 serum levels were measured by ELISA and the megakaryocytic production s tudied by immunohistochemistry, reverse hemolytic plague assay (RHPA) toget her with reverse transcription/polymerase chain reaction (RT-PCR) in highly enriched megakaryocyte preparations. in additional experiments, the influe nce of IL-3 stimulation and the expression of IL-6R were tested. Serum leve ls of IL-6 did not differ between the three groups under study. In contrast , immunohistochemistry revealed a raised proportion of megakaryocytes expre ssing IL-6 in PV as compared to normal donors and patients suffering from P G. The percentage of megakaryocytes actively secreting this cytokine as det ected by the RHPA was 20 times greater than in both the other groups. This phenomenon was further substantiated by the fact that IL-6 mRNA could only be shown in PV megakaryocyte preparations. The regulation of IL-6 secretion appears to be abnormal in PV. Whereas in the normal and in the PG group IL -3 stimulation exerts a marked increase in megakaryocytic IL-6 secretion, P V megakaryocytes responded with a paradoxical down-regulation of IL-6 synth esis combined with the loss of IL-6R. Our data describe for the first time an abnormally raised IL-6 production by PV megakaryocytes and point towards fundamental regulatory alterations of the IL-6 synthesis in this disease.