We have recently found that soluble biglycan purified from rat thymic myoid
cells had haemopoietic activity capable of inducing preferential growth an
d differentiation of monocytic lineage cells from various haemopoietic sour
ces, including brain microglial cells. In the present study, to understand
developmental mechanisms of microglial/monocytic cells in the brain, we hav
e attempted to identify haemopoietic activity of the brain biglycan. The mR
NA and the immunological epitope of biglycan were detected in the rat brain
homogenates and several rat glial cell lines. Immunohistochemical study sh
owed that several different types of brain cells produced biglycan. During
development biglycan synthesis in the brain appeared to be increased. The b
rain haemopoietic biglycan was easily separated by DEAE-Sepharose chromatog
raphy from the macrophage colony stimulating factor (M-CSF) which was conco
mitantly produced from the brain cells. The brain haemopoietic biglycan, pu
rified through immunoaffinity column, indeed stimulated growth of primarily
cultured microglial cells. Taken together, these results suggest that the
haemopoietic biglycan plays an important role in generating brain-specific
circumstances for development of microglial/monocytic cells. (C) 2000 Elsev
ier Science B.V. All rights reserved.