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PMID: 12899713 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

CXCR4 chemokine receptors (CD184) and alpha4beta1 integrins mediate spontaneous migration of human CD34+ progenitors and acute myeloid leukaemia cells beneath marrow stromal cells (pseudoemperipolesis).

British journal of haematology ·Vol. 122 ·No. 4 ·2003-08-00 ·Pages 579-89

Burger JA, Spoo A, Dwenger A, Burger M, Behringer D

Abstract

Marrow stromal cells play an important role in regulating the development and proliferation of haematopoietic stem cells (HSC) within the marrow microenvironment. However, the molecular mechanisms of stem cell-stromal cell interactions are not fully understood. We observed that mobilized peripheral blood and cord-blood-derived CD34+ progenitor cells, or CD34+ acute myeloid leukaemia (AML) cells spontaneously migrated beneath marrow stromal cells, an in vitro migration phenomenon termed pseudoemperipolesis. In contrast, the CD34+ myeloid leukaemia cell line, Kasumi-1, did not display pseudoemperipolesis. Cord blood CD34+ cells had a higher capacity than granulocyte-colony-stimulating-factor-mobilized CD34+ cells for pseudoemperipolesis (28.7 +/- 12%vs 18.1 +/- 6.1% of input cells within 24 h, mean +/- SD, n = 8), whereas 9.4 +/- 12.6% (mean +/- SD, n = 10) of input AML cells displayed this phenomenon. Pseudoemperipolesis of CD34+ progenitor and AML cells was significantly inhibited by pertussis toxin and antibodies to the CXCR4 chemokine receptor (CXCR4, CD184), but not control antibodies. Moreover, CD34+ and AML cell migration was significantly inhibited by a CS1 peptide that blocks alpha4beta1 integrin binding, but not by a control peptide, in which the fibronectin binding motif was scrambled. Pseudoemperipolesis was associated with an increased proliferation of migrated CD34+ progenitor cells but not AML cells within the stromal layer, demonstrated by cell cycle analysis and cell division tracking. We conclude that alpha4beta1 integrin binding and CXCR4 chemokine receptor activation are prerequisites for the migration of CD34+ haematopoietic progenitors and AML cells beneath marrow stromal cells. These observations suggest a central role of marrow stromal cells for HSC trafficking and homing within the marrow microenvironment.

MeSH Terms
Antigens, CD34/analysis Bone Marrow Cells/physiology Cell Cycle/physiology Cell Division/physiology Cell Movement Coculture Techniques Flow Cytometry/methods Hematopoietic Stem Cells/physiology Humans Integrin alpha4beta1/physiology Leukemia, Myeloid/pathology Ligands Receptors, CXCR4/physiology Stromal Cells/physiology Tumor Cells, Cultured
Chemicals
Antigens, CD34 Integrin alpha4beta1 Ligands Receptors, CXCR4
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Burger Jan A
Division of Haematology/Oncology, Department of Medicine, Freiburg University Hospital, Hugstetterstrasse 55, D-79106 Freiburg, Germany. burger@mm11.ukl.uni-freiburg.de
Spoo Anke
Dwenger Anne
Burger Meike
Behringer Dirk
Article Info
Journal
British journal of haematology
Abbr.
Br J Haematol
ISSN
0007-1048
Published
2003-08-00
Pages
579-89
Language
English
Region
England
NLM ID
0372544
Subset
IM
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