Objective. The hematopoietic microenvironment is complex, and the role of m
yofibroblast in its function is crucial. In order to obtain a stable model
reflecting this particular cell type, we have previously established human
bone marrow cell lines from primary myofibroblastic Strol(+) population (pS
trol(+)). We placed HPV16 E6 and E7 expression under the control of differe
nt promoters. Here, we have characterized and studied the hematopoietic sup
port for two cell lines corresponding to the promoters alpha -SM (alpha SM-
56 line) and SV40 (SV40-56 line). Materials and Methods. The expression pro
file was analyzed at the RNA level by gene array and at the protein level b
y Western blot, flow cytometry, and ELISA, Hematopoietic support determined
using colony-forming unit (CFU) and stroma-adherent colony-forming cell (S
A-CFC) assays. Results. The phenotype of cell lines was not significantly m
odified compared with primary myofibroblastic cells. They secreted a broad
spectrum of hematopoietic cytokines and nonspecific mediators, The two Line
s allowed the growth of hematopoietic precursors and had different support
capabilities. Conclusions, We have extensively characterized two novel huma
n bone marrow stromal cell lines. They retained a myofibroblastic phenotype
and have substantial but different hematopoietic support capabilities. The
se lines provided a basis for determining stromal factors involved in stem-
tell regulation. (C) 2001 International Society for Experimental Hematology
, Published by Elsevier Science Inc.