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Induction of CD45 Expression and Proliferation in U-266 Myeloma Cell Line by Interleukin-6

Research Authors
Maged S. Mahmoud, Hideaki Ishikawa, Ryuichi Fujii, and Michio M. Kawano
Research Date
Research Journal
Blood
Research Member
Research Publisher
The American Society of Hematology
Research Vol
92 (10)
Research Year
1998
Research_Pages
3887-3897
Research Abstract

Recently, there has been an increasing interest in the expression pattern and biological significance of the CD45 molecule in myeloma cells. In this study, we have further defined the phenotypic pattern of CD45 expression on myeloma cells. Using a panel of myeloma cell lines, we showed that CD45 showed a remarkably heterogeneous pattern of expression. Whereas some cell lines were CD451 and others were CD452, the U-266 cell line, although predominantly CD452, still had a considerable subpopulation of CD451 cells. Among the myeloma cell lines examined, there was a direct correlation between interleukin-6 (IL-6) dependency and CD45 positivity. Moreover, we showed that IL-6 stimulation led to the induction of expression of CD45 and cellular proliferation. Using independent experimental approaches, we could show that the IL-6–induced effects were closely linked to CD45 expression. First, sorting out CD451 and CD452 subsets of U-266 cell line followed by IL-6 stimulation, only the CD451 cells showed a proliferative advantage after IL-6 stimulation. Second, IL-6 stimulation of sorted CD452 cells was gradually followed by phenotypic conversion to CD451 cells that started after 2 days as judged by the detection of CD45 mRNA by reverse transcription polymerase chain reaction (RT-PCR) and immunophenotypic analysis by flow cytometry. Withdrawal of IL-6 from the medium led to gradual loss of CD45 expression in CD451 flow-sorted U-266 cells. Third, the use of vanadate, a potent inhibitor of protein tyrosine phosphatase (PTP), abrogated the IL-6–induced proliferation in the CD451 myeloma cells. On the other hand, cellular proliferation induced by IL-6 was not affected by the serine-threonine phosphatase inhibitor okadaic acid. Our data show that the expression pattern of CD45 in myeloma cell lines is heterogeneous and show for the first time that CD45 expression can be induced by IL-6 stimulation. Finally, these data shed some light on the biological role of CD45 in myeloma by determining the proliferative population among myeloma cells.