We have a previously reported that interleukin-10 (IL-10) is a potent but IL-6-unrelated growth factor for freshly explanted myeloma cells (Lu et al, Blood 85:2521, 1995). We have also shown that exogenous IL-10 supported the growth of XG-1 and XG-2 human myeloma cell lines (HMCL) through an IL-6-independent mechanism. (Lu et al, Blood 85:2521, 1995). Because the IL-10 receptor does not involve the gp 130 IL-6 transducer, we have attempted to elucidate the mechanisms of IL-10 action on myeloma cells. Our results indicate that the myeloma cell growth factor activity of IL-10 was abrogated by an antibody to the gp 130 IL-6 transducer, indicating that it was mediated through one of the gp 130-activating cytokines. We found that myeloma cells from XG-1 and XG-2 HMCL and from 5 of 6 patients' tumoral samples produced oncostatin M (OM) constitutively but failed to produce IL-6, IL-11 and leukemia- inhibitory factor (LIF). The autocrine OM was inactive in the absence of IL-10 due to lack of a functional OM receptor on myeloma cells. IL- 10, by inducing the receptor for LIF (LIFR), produced a functional autocrine OM loop in XG-1 and XG-2 cells and in primary myeloma cells from 2 patients. We also found that some myeloma cell lines (XG-4, XG- 6, and XG-7) an fresh myeloma cells from 3 of 6 patients produced an autocrine IL-10 and that these cells constitutively expressed LIFR. One HMCL (XG-7) produced IL-10, OM, and IL-6 an expressed LIFR. The XG-7 cells used OM and IL-6 as autocrine growth factors. We have previously shown that IL-10 could induce IL-11 receptor in myeloma cells and confer on them sensitivity to IL-11 (Lu et al, FEBS Lett 377:515, 1995). Taken together, these results show that IL-10 is a key cytokine for inducing the expression of LIFR and IL-11R and possibly another uncharacterized OM coreceptor on myeloma cells and that OM and IL-10 might be produced by myeloma cells. They also emphasize that all myeloma cell growth factors reported to data involve an activation of the gp130 IL-6 transducer.
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November 15, 1996
Interleukin-10 is a growth factor for human myeloma cells by induction of an oncostatin M autocrine loop
ZJ Gu,
ZJ Gu
Institute for Molecular Genetics, Montpellier, France.
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V Costes,
V Costes
Institute for Molecular Genetics, Montpellier, France.
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ZY Lu,
ZY Lu
Institute for Molecular Genetics, Montpellier, France.
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XG Zhang,
XG Zhang
Institute for Molecular Genetics, Montpellier, France.
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V Pitard,
V Pitard
Institute for Molecular Genetics, Montpellier, France.
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JF Moreau,
JF Moreau
Institute for Molecular Genetics, Montpellier, France.
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R Bataille,
R Bataille
Institute for Molecular Genetics, Montpellier, France.
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J Wijdenes,
J Wijdenes
Institute for Molecular Genetics, Montpellier, France.
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JF Rossi,
JF Rossi
Institute for Molecular Genetics, Montpellier, France.
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B Klein
B Klein
Institute for Molecular Genetics, Montpellier, France.
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Blood (1996) 88 (10): 3972–3986.
Citation
ZJ Gu, V Costes, ZY Lu, XG Zhang, V Pitard, JF Moreau, R Bataille, J Wijdenes, JF Rossi, B Klein; Interleukin-10 is a growth factor for human myeloma cells by induction of an oncostatin M autocrine loop. Blood 1996; 88 (10): 3972–3986. doi: https://doi.org/10.1182/blood.V88.10.3972.bloodjournal88103972
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November 15 1996
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