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Stem Cell Center, Lund University

Integrin α2 and Akt in early hematopoiesis

Abstract

dc:description

Hematopoiesis is a tightly regulated process in which hematopoietic stem cells reside at the apex of the hierarchy, and produce all kinds of mature blood cells by differentiation to replenish the cell loss in homeostasis and acute injury. In past few decades, much effort has been made to purify hematopoietic stem cells (HSCs) and lineagecommitted progenitor cells both in mouse and human, enabling further characterization of these cell populations not only in normal hematopoiesis, but also in various hematological malignancies. However, while the isolation of different cell populations in mouse hematopoietic system is achieved with a very high purity, purification of human hematopoietic stem and progenitor cells still far lags behind. Integrins are heterodimeric transmembrane protein receptors regulating many important cellular processes including homing of HSCs by binding to neighboring cells or extracellular matrix proteins. First, we showed that integrin α2 is a novel marker improving the prospective isolation of human cord blood HSCs. We found integrin α2 receptor was preferentially expressed in cord blood-derived CD34+CD38-CD90+ in vivo long-term repopulating cells, demonstrated by 24-week limiting-dilution xenotransplantations using immunodeficient mice. Second, we revealed that integrin α2, which is a marker for megakaryoctyes and platelets, was not expressed in the immature CD34+CD38-CD45RA- bipotential megakaryocyte-erythrocyte progenitors in human bone marrow, providing a means for enriching this novel bipotent progenitor population for further studies on early megakaryocytic and erythroid lineage fate decisions. In addition, we demonstrated that hyperactivation of Akt, which is a key intrinsic factor regulating the homeostasis of HSCs, was incompatible with the survival and growth promoting ability of FMS-like tyrosine kinase 3-internal tandem duplication (FLT3-ITD) signaling in murine stem and progenitor cells. Prospective isolation of more homogenous stem and progenitor cell populations in human and understanding the instrinsic regulation of HSC homeostasis will give important insights into the HSC maintenance and fate decisions in normal hematopoiesis, as well as the pathogenesis of various hematological disorders.

Degree

thesis:*
Grantor dc:publisher
Stem Cell Center, Lund University
Year dc:date
2013

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Wong, Wan Man

Subjects

dc:subject × 1

Rights

dc:rights
Statement dc:rights
  • info:eu-repo/semantics/openAccess
Language dc:language
eng

Identifiers

dc:identifier.*
Identifier
urn:isbn:978-91-87651-19-9
OAI identifier oai:identifier
oai:lup.lub.lu.se:11edcfae-2131-48ea-ac8b-a9a7f47dccaa

Chain of custody

source
Harvested from
University of Lund
Base URL
lup.lub.lu.se/oai
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Wong, Wan Man. Integrin α2 and Akt in early hematopoiesis. Stem Cell Center, Lund University, 2013. https://lup.lub.lu.se/record/4174628