R. Klein et W. Roggendorf, Increased microglia proliferation separates pilocytic astrocytomas from diffuse astrocytomas: a double labeling study, ACT NEUROP, 101(3), 2001, pp. 245-248
It is not known how many non-tumorous cells in gliomas contribute to the pr
oliferation rate. We investigated the proliferative activity of microglia i
n an immunohistochemical double-labeling study of pilocytic astrocytomas an
d astrocytomas WHO grade II-IV using the antibodies MIB-1 (Ki67) as prolife
ration-marker and Ki-M1P (CD68) as microglia marker. We found the highest i
ndices of proliferating microglia in pilocytic astrocytomas with an average
rate of 32% (+/-6.8) of all proliferating cells. In contrast, the prolifer
ation indices of microglia were lowest in fibrillary astrocytomas with 8.6%
(+/-2.5) of all proliferating cells. In anaplastic astrocytomas and gliobl
astomas the percentage of proliferating microglia showed a slight increase
to 8.8% (+/-3.6) and 13.4% (+/-8.7), respectively. We conclude that microgl
ial cells in astrocytic brain tumors proliferate and show different prolife
rative activities at different grades of malignancy with the highest rates
of proliferating microglia especially in pilocytic astrocytomas. Thus, the
proliferation rate does not solely reflect the proliferation of tumor cells
, but also of non-tumorous cells. This should be considered in particular w
hen proliferation rates are used as a criterion for prognosis and grading o
f pilocytic astrocytomas.