Segregation of lipid raft markers including CD133 in polarized human hematopoietic stem and progenitor cells

Author:

Giebel Bernd1,Corbeil Denis1,Beckmann Julia1,Höhn Johannes1,Freund Daniel1,Giesen Kay1,Fischer Johannes1,Kögler Gesine1,Wernet Peter1

Affiliation:

1. From the Institut für Transplantationsdiagnostik and Zelltherapeutika, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany; Medical Clinic and Polyclinic I, University Carl Gustav Carus, Dresden, Germany; and Max-Planck-Institute of Molecular Cell Biology and Genetics, Dresden, Germany.

Abstract

AbstractDuring ontogenesis and the entire adult life hematopoietic stem and progenitor cells have the capability to migrate. In comparison to the process of peripheral leukocyte migration in inflammatory responses, the molecular and cellular mechanisms governing the migration of these cells remain poorly understood. A common feature of migrating cells is that they need to become polarized before they migrate. Here we have investigated the issue of cell polarity of hematopoietic stem/progenitor cells in detail. We found that human CD34+ hematopoietic cells (1) acquire a polarized cell shape upon cultivation, with the formation of a leading edge at the front pole and a uropod at the rear pole; (2) exhibit an amoeboid movement, which is similar to the one described for migrating peripheral leukocytes; and (3) redistribute several lipid raft markers including cholesterol-binding protein prominin-1 (CD133) in specialized plasma membrane domains. Furthermore, polarization of CD34+ cells is stimulated by early acting cytokines and requires the activity of phosphoinositol-3-kinase as previously reported for peripheral leukocyte polarization. Together, our data reveal a strong correlation between polarization and migration of peripheral leukocytes and hematopoietic stem/progenitor cells and suggest that they are governed by similar mechanisms.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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