Six well-characterized specimens of cultured astrocytoma cells were in
vestigated with a panel of macrophage markers. Our results show that t
he macrophage markers OKM-1(CD11b), OKM5(CD36), EBM11(CD68), HAM56, Fa
ctor 13, alpha-1-antichymotrypsin, alpha-1-antitrypsin, ferritin and l
ysozyme are clearly reactive to neoplastic astrocytes whereas astrocyt
es in normal brain specimens are not reactive. In order to obtain furt
her confirmation concerning the reactivity of tumor cells in vivo, we
simultaneously measured by flow cytometric analysis DNA content and HA
M56 immunoreactivity in a freshly obtained tumor specimen. In this exp
eriment we found a marked reactivity of aneuploid cells to HAM56. The
macrophage phenotype of malignant astrocytes may reflect a similarity
in functions of these cells and tumor-associated macrophages which pro
mote tumor growth via the production of growth factors and angiogenic
factors. Furthermore, our findings implicate that demonstration of mac
rophages within malignant astrocytomas by using macrophage-specific an
tibodies must be cautiously considered.