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Blood, Vol. 92 No. 3 (August 1), 1998:
pp. 894-900
Role of Adhesion Molecules in the Homing and Mobilization of Murine
Hematopoietic Stem and Progenitor Cells
Monica Vermeulen,
Françoise Le Pesteur,
Marie-Claude Gagnerault,
Jean-Yves Mary,
Françoise Sainteny, and
Françoise Lepault
From the CNRS URA 1461, Université Paris V, Hôpital
Necker, Paris; INSERM U 362, Institut Gustave Roussy, Villejuif; and
INSERM U 444, Faculté de Médecine Saint Antoine, Paris,
France.
Bone marrow (BM) transplantation still must overcome multiple
difficulties and should benefit from better understanding of stem-cell
homing and mobilization. Here, we analyzed the involvement of several
adhesion molecules in the two processes by treating mice with
monoclonal antibodies against these molecules. Treatment of lethally
irradiated mice grafted with isogeneic BM cells showed that at least
two migration pathways are important for stem-cell homing to the BM,
whereas only one of them is involved in lodging of colony-forming
unit-spleen (CFU-S) in the spleen. We confirm that the VLA-4/VCAM-1
adhesion pathway is important for stem-cell homing to the BM only and
show that CD44 is involved in CFU-S lodging in both BM and spleen.
These results show that entry of CFU-S into the spleen is regulated.
The observation that when one migration pathway is altered, CFU-S do
not enter the BM via the other pathway may indicate that the two
mechanisms involved in CFU-S homing into the BM are linked. The
adhesion molecules VLA-4 and CD44 are also implied in the mobilization
of stem cells into the blood stream of mice injected once with
anti-VLA-4 or anti-CD44. Anti-VLA-4 administration led to a
significant increase in circulating stem cells as early as 8 hours
after treatment. Stem cells mobilized by anti-VLA-4 comprise cells
with high self-renewal potential and thus may be used for long-term
reconstitution of the hematopoietic tissue.
© 1998 by The American Society of Hematology.

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