The bone marrow stroma consists of a heterogeneous population of cells that
provide the structural and physiological support for hematopoietic cells.
Additionally, the bone marrow stroma contains cells with a stem-cell-like c
haracter that allows them to differentiate into bone, cartilage, adipocytes
, and hematopoietic supporting tissues. Several experimental approaches hav
e been used to characterize the development and Functional nature of these
cells in vivo and their differentiating potential in vitro. In vivo, presum
ptive osteogenic precursors have been identified by morphologic and immunoh
istochemical methods. In culture, the stromal cells can be separated from h
ematopoietic cells by their differential adhesion to tissue culture plastic
and their prolonged proliferative potential. In cultures generated from si
ngle-cell suspensions of marrow, bone marrow stromal cells grow in colonies
, each derived From a single precursor cell termed the colony-forming unit-
fibroblast. Culture methods have been developed to expand marrow stromal ce
lls derived From human, mouse, and other species. Under appropriate conditi
ons, these cells are capable of Forming new bone after in vivo transplantat
ion. Various methods of cultivation and transplantation conditions have bee
n studied and found to have substantial influence on the transplantation ou
tcome. The finding that bone marrow stromal cells can be manipulated in vit
ro and subsequently form bone in vivo provides a powerful new model system
for studying the basic biology of bone and for generating models for therap
eutic strategies aimed at regenerating skeletal elements.