Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Blood ; 101(8): 2924-31, 2003 Apr 15.
Article in English | MEDLINE | ID: mdl-12480697

ABSTRACT

Precise analysis of human CD34-negative (CD34(-)) hematopoietic stem cells (HSCs) has been hindered by the lack of a simple and reliable assay system of these rare cells. Here, we successfully identify human cord blood-derived CD34(-) severe combined immunodeficiency (SCID)- repopulating cells (SRCs) with extensive lymphoid and myeloid repopulating ability using the intra-bone marrow injection (IBMI) technique. Lineage-negative (Lin(-)) CD34(-) cells did not show SRC activity by conventional tail-vein injection, possibly due to their low levels of homing receptor expression and poor SDF-1/CXCR4- mediated homing abilities, while they clearly showed a high SRC activity by IBMI. They generated CD34(+) progenies not only in the injected left tibia but also in other bones following migration. Moreover, they showed slower differentiating and reconstituting kinetics than CD34(+) cells in vivo. These in vivo-generated CD34(+) cells showed a distinct SRC activity after secondary transplantation, clearly indicating the long-term human cell repopulating capacity of our identified CD34(-) SRCs in nonobese diabetic (NOD)/SCID mice. The unveiling of this novel class of primitive human CD34(-) SRCs by IBMI will provide a new concept of the hierarchy in the human HSC compartment and has important implications for clinical HSC transplantation as well as for basic research of HSC.


Subject(s)
Bone Marrow , Cord Blood Stem Cell Transplantation , Hematopoietic Stem Cells/cytology , Animals , Antigens, CD34/analysis , Bone Marrow Transplantation , Cell Lineage , Cell Movement , Cell Separation , Clone Cells/transplantation , Colony-Forming Units Assay , Graft Survival , Humans , Infant, Newborn , Injections , Lymphocytes/cytology , Mice , Mice, Inbred NOD , Mice, SCID , Myeloid Cells/cytology , Receptors, CXCR4/analysis , Severe Combined Immunodeficiency/pathology , Transplantation Chimera , Transplantation, Heterologous
SELECTION OF CITATIONS
SEARCH DETAIL
...