Tv. Michurina et Ng. Khrushchov, EXPERIMENTAL-ANALYSIS OF CELL-INTERACTIONS DURING HEMATOPOIESIS, The International journal of developmental biology, 41(6), 1997, pp. 817-833
The principal approach was to study hemopoiesis on different stromal c
ell underlayers (fibroblasts or fibroblast-like cells covering a forei
gn body implanted into the peritoneal cavity of mice or other rodents)
after intraperitoneal transplantation of syngeneic, allogeneic, and x
enogeneic hemopoietic cells. The data obtained are compared with the r
esults of experiments on repopulation of ectopic hemopoietic territori
es (under the mouse kidney capsule) by syngeneic and xenogeneic hemopo
ietic cells. Competitive cell interactions are described that occur du
ring repopulation of the hemopoietic stroma or formation of the hemopo
ietic foci on cellulose acetate membranes (CAMs) in the peritoneal cav
ity of irradiated mice by genetically different hemopoietic cells tran
splanted to these animals (multicomponent radiation chimeras). The mod
el of xenogeneic and multicomponent radiation chimeras was reproduced
in long-term bone marrow cultures, where hemopoietic cells of differen
t genotypes coexisted, without any competitive cell elimination. The s
econd part of this review deals with hemopoiesis on stromal cell under
layers, formed by cells of different origin, different stages of devel
opment, and obtained from other sources. These underlayers were formed
on CAMs in vitro and then transferred into the peritoneal cavity of i
rradiated mice, which subsequently received intraperitoneal injections
of donor hemopoietic cells. Specific features of hemopoiesis on strom
al underlayers formed by the following cell types are described: (1) f
ibroblasts from mouse embryos at different developmental stages; (2) f
ibroblasts from the skin, liver, and bone marrow of 17-day mouse fetus
es and newborn mice; (3) fibroblasts from the monolayer cultures of mo
use and rat bone marrow; (4) 3T3 cell line; (5) hepatocytes of 17-day
mouse fetuses or sexually mature rats; (6) newborn mouse kidney cells;
and (7) cells transgenic for the erythropoietin gene. The phenomena o
bserved in these experiments and their probable mechanisms are discuss
ed.