Recently, cytokines and interleukins such as SCF, GM-CSF, G-CSF, TGF-beta,
IL-6, IL-7, IL-8, IL-11 have been reported to be elaborated by endothelial
cells. For further study, serum free bone marrow endothelial cell condition
ed medium (BMEC-CM) was collected and ultrafiltrated by using a centriprep
10. The concentrated retentate (R-BMEC-CM) contained some substances whose
molecular weight was more than 10 000 daltons. The filtrate (F-BMEC-CM) con
tained some substances whose molecular weight was less than 10 000 daltons.
The effects of R-BMEC-CM and F-BMEC-CM on the growth of haematopoietic pro
genitors and the expression of cytokine and interleukin mRNAs of BMEC were
investigated. The results showed that R-BMEC-CM stimulated the growth of CF
U-GM, HPP-CFC, BFU-E, CFU-E, and CFU-Meg; while F-BMEC-CM inhibited the gro
wth of these progenitors. Using the method of hybridizing to the Atlas cDNA
Array, we were able to detect the presence of mRNAs of cytokines and inter
leukins in bone marrow endothelial cells. Our finding of the existence of m
RNAs of SCF, GM-CSF, IL-6, TGF-beta, IL-1, and IL-11 in these cells was in
agreement with the data reported previously. Furthermore, we detected mRNAs
of MIP-2, Thymosion-beta 4, PDGF, MSP-1, IFN-gamma, IL-13 and inhibin, whi
ch are related to haematopoiesis. Among these cytokines and interleukins, S
CF, GM-CSF, IL-6, IL-1, and IL-11 are haematopoietic stimulators which may
be responsible for the stimulative effects on the growth of haematopoietic
progenitors. One of our new findings, the thymosin-beta 4, is a small molec
ular haematopoietic inhibitor. It may be responsible for the inhibitory eff
ect of F-BMEC-CM on haematopoietic progenitors. The presence of mRNAs of BM
P, MSP-1, MIP-2, PDGF and IL-13 suggests that bone marrow endothelial cells
might elaborate these substances. Their influence on haematopoietic progen
itors needs further study. (C) 2000 Academic Press.