B cells differentiate into plasma cells which produce antibodies in the bon
e marrow (BM). Multiple myeloma (MM) is a hematologic malignancy in human p
lasma cells, and myeloma cells grow mainly in BM. According to phenotypic d
ifferences, such as expression of adhesion molecules, human myeloma cells a
s well as normal plasma cells can be classified into several differentiatio
n stages. We have found that cells strongly expressing CD38 antigens (CD38(
+ + +)) in BM are all plasma cells, and that there also are no plasma cells
in either CD38 (-) cell fraction or fraction of cells weakly expressing CD
38 antigens (CD38 (+)). Myeloma cells in BM consist of CD38 (+) (+ +) MPC-1
(-) CD49e (VLA-5) (-) immature and CD38 (+) (+) (+) MPC-1 (+) CD49e (+) ma
ture myeloma cells. Immature myeloma cells proliferate markedly in vitro an
d respond to interleukin-6 (IL-6), a growth factor for myeloma cells, where
as mature myeloma cells show very low proliferative activities and show no
response to IL-6. Immature myeloma cells expressing CD21 molecules on their
surface seem to attach to stromal cells in BM through binding to CD23 mole
cules. Thus, there is a heterogeneity in human myeloma cells, and immature
myeloma cells appear to proliferate in response to IL-6. (C) 1998 Elsevier
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