TY - JOUR
T1 - VLA‐4 and VCAM‐1 are the principal adhesion molecules involved in the interaction between blast colony‐forming cells and bone marrow stromal cells
AU - Oostendorp, Robert A.J.
AU - Reisbach, Gilbert
AU - Spitzer, Elisabeth
AU - Thalmeier, Karin
AU - Dienemann, Hendrik
AU - Mergenthaler, Hans‐Günther ‐G
AU - Dörmer, Peter
PY - 1995/10
Y1 - 1995/10
N2 - Summary. The molecular basis and functional significance of interactions between haemopoietic progenitor cells and the stromal microenvironment is still poorly understood. Here we investigated a broad panel of surface adhesion molecules for their involvement. For this purpose, the colony‐forming capacity of stroma‐adherent Bl‐CFC, BFU‐E and GM‐CFC was studied. Both mononuclear bone marrow cells (BMC) and bone marrow‐derived stromal cells (BMSC) express a wide variety of adhesion molecules. However, only antibodies against β1‐, α4‐integrin (both chains of the very late activation antigen‐4 (VLA‐4)) and vascular cell adhesion molecule (VCAM‐1) inhibited colony formation from stroma‐adherent Bl‐CFC by 50% or more. Antibodies against a panel of other adhesion molecules, including the α5‐integrin chain, were without effect. Subsequent pretreatment experiments revealed that VLA‐4 on progenitors interacted with stromal VCAM‐1. The inhibitory antibodies did not interfere with the clonogenic capacity of but with adhesion of BFU‐E and GM‐CFC. Whether the inhibitory antibodies act similarly on progenitors which depend on BMSC for growth and/or differentiation, such as Bl‐CFC, remains to be determined.
AB - Summary. The molecular basis and functional significance of interactions between haemopoietic progenitor cells and the stromal microenvironment is still poorly understood. Here we investigated a broad panel of surface adhesion molecules for their involvement. For this purpose, the colony‐forming capacity of stroma‐adherent Bl‐CFC, BFU‐E and GM‐CFC was studied. Both mononuclear bone marrow cells (BMC) and bone marrow‐derived stromal cells (BMSC) express a wide variety of adhesion molecules. However, only antibodies against β1‐, α4‐integrin (both chains of the very late activation antigen‐4 (VLA‐4)) and vascular cell adhesion molecule (VCAM‐1) inhibited colony formation from stroma‐adherent Bl‐CFC by 50% or more. Antibodies against a panel of other adhesion molecules, including the α5‐integrin chain, were without effect. Subsequent pretreatment experiments revealed that VLA‐4 on progenitors interacted with stromal VCAM‐1. The inhibitory antibodies did not interfere with the clonogenic capacity of but with adhesion of BFU‐E and GM‐CFC. Whether the inhibitory antibodies act similarly on progenitors which depend on BMSC for growth and/or differentiation, such as Bl‐CFC, remains to be determined.
KW - VCAM‐1
KW - VLA‐4
KW - adhesion
KW - haemopoiesis
KW - stroma
UR - http://www.scopus.com/inward/record.url?scp=0028877176&partnerID=8YFLogxK
U2 - 10.1111/j.1365-2141.1995.tb05290.x
DO - 10.1111/j.1365-2141.1995.tb05290.x
M3 - Article
C2 - 8547062
AN - SCOPUS:0028877176
SN - 0007-1048
VL - 91
SP - 275
EP - 284
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 2
ER -