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Stimulation of Mouse and Human Primitive Hematopoiesis by Murine Embryonic Aorta-Gonad-Mesonephros–Derived Stromal Cell Lines

Authors :
Xu, M. -J
Tsuji, K.
Ueda, T.
Yoh-suke Mukouyama
Hara, T.
Yang, F. -C
Ebihara, Y.
Matsuoka, S.
Manabe, A.
Kikuchi, A.
Ito, M.
Miyajima, A.
Nakahata, T.
Source :
Scopus-Elsevier
Publication Year :
1998
Publisher :
American Society of Hematology, 1998.

Abstract

We report here on a novel stromal cell line, AGM-S3, derived from the aorta-gonad-mesonephros (AGM) region of a 10.5 days postcoitum (dpc) mouse embryo. The AGM-S3 cells promoted production of hematopoietic progenitors and day-12 spleen colony-forming cells from Lin−c-Kit+Sca-1+ murine primitive hematopoietic cells. They also supported for 6 weeks generation of human multipotential progenitors from cord blood CD34+CD38− primitive hematopoietic cells. Human long-term repopulating hematopoietic stem cells (LTR-HSC) with the potential to reconstitute hematopoiesis in NOD/SCID mice were maintained on AGM-S3 cells for at least 4 weeks. Flow cytometric analysis showed that CD13, vascular cellular adhesion molecule-1, and Sca-1 were expressed on AGM-S3 cells. Because stem cell factor, interleukin-6 (IL-6), and oncostatin M, but not IL-3, IL-11, leukemia- inhibitory factor, granulocyte colony-stimulating factor, granulocyte-macrophage colony-stimulating factor, thrombopoietin, and Flk2 ligand were detected in reverse transcription-polymerase chain reaction analysis of AGM-S3 cells, the cells seem to express species-cross reactive molecule(s) other than the cytokines examined and which act on primitive hematopoietic progenitor/stem cells. This cell line is expected to elucidate molecular mechanisms regulating early hematopoiesis and pave the way for developing strategies for expansion of human transplantable HSC.© 1998 by The American Society of Hematology.

Details

ISSN :
15280020 and 00064971
Volume :
92
Database :
OpenAIRE
Journal :
Blood
Accession number :
edsair.doi.dedup.....9fa3af3918edf422ecafa911d411f071
Full Text :
https://doi.org/10.1182/blood.v92.6.2032.418k29_2032_2040