Activation of mitogen-activated protein kinase through alpha 5/beta 1 integrin is required for cell cycle progression of B progenitor cell line, Reh,on human marrow stromal cells
Yw. Qiang et al., Activation of mitogen-activated protein kinase through alpha 5/beta 1 integrin is required for cell cycle progression of B progenitor cell line, Reh,on human marrow stromal cells, EXP HEMATOL, 28(10), 2000, pp. 1147-1157
Objective. Attachment to bone marrow (BM) stromal cells is crucial for the
normal growth and development of B-cell progenitors (pro-B), However, the m
olecular mechanisms by which contact facilitates the proliferation of pro-B
cells are not completely understood. This study was performed to investiga
te this interaction.
Materials and Methods, A model pro-B cell line (Reh) and a human BM stromal
cell line (KM102) were used. Flow cytomery was used for cell cycle analysi
s. Western Blotting and immunoprecipitation were utilized to examine the le
vels of cyclin-dependent kinase (cdk) and p27(Kip1).
Results. Attachment to both KM102 and normal BM stromal cells significantly
promoted the growth of Reh cells. Pretreatment of Reh cells with anti-inte
grin beta 1 or alpha 5 monoclonal antibody (mAb), but not alpha 4 or ICAM-1
mAb, abrogated this enhancement of proliferation. Furthermore, stroma atta
chment resulted in shortening of the G(1) phase of cell cycle, significant
increases cdk2 activity, degradation of cdk inhibitor p27-GST protein, and
decrease in levels of p27(Kip1) protein. In addition, solid-phase cross-lin
king of alpha 5 via immobilized antibody also resulted in extracellular sig
nal-regulated (ERK)-2 kinase phosphorylation, increase in cdk2 activity, de
crease in levels of p27(Kip1) protein, and enhanced proliferation that was
inhibited by treatment with PD98059, a specific ERK inhibitor.
Conclusion. Integrin alpha 5 beta 1-mediated stroma contact promotes the pr
oliferation of B-cell progenitors through the activation of ERK-2, which in
turn modulates cell cycle regulation machinery including induction of cdk2
activity and degradation of p27(Kip1) and contributing to acceleration of
the G(1) phase of cell cycle progression. (C) 2000 International Society fo
r Experimental Hematology. Published by Elsevier Science Inc.