Molecular Study of Interactions between Hematopoietic Stem Cells and Stromal Cells

Multipotent hematopoietic stem cells (HSCs) are progenitors of all types of hematopoietic cells, and the efficient isolation and propagation of HSCs will significantly enhance our ability to manage many human disorders with bone marrow transplantation, stem cell transplantation and gene therapy. We...

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Main Authors: Luo, Biao, Meng-Ling, Choong, Heard, Amanda, Li, Zhe, Moore, Kateri, Kaiser, Chris, Lemischka, Ihor R., Yap, Miranda G.S., Lodish, Harvey F.
Format: Article
Language:en_US
Published: 2003
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Online Access:http://hdl.handle.net/1721.1/4044
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author Luo, Biao
Meng-Ling, Choong
Heard, Amanda
Li, Zhe
Moore, Kateri
Kaiser, Chris
Lemischka, Ihor R.
Yap, Miranda G.S.
Lodish, Harvey F.
author_facet Luo, Biao
Meng-Ling, Choong
Heard, Amanda
Li, Zhe
Moore, Kateri
Kaiser, Chris
Lemischka, Ihor R.
Yap, Miranda G.S.
Lodish, Harvey F.
author_sort Luo, Biao
collection MIT
description Multipotent hematopoietic stem cells (HSCs) are progenitors of all types of hematopoietic cells, and the efficient isolation and propagation of HSCs will significantly enhance our ability to manage many human disorders with bone marrow transplantation, stem cell transplantation and gene therapy. We employed "Signal Sequence Trap (SST)" method with yeast invertase to clone proteins on the surface of or secreted by stromal cells that enhance or inhibit the propagation of HSC’s in culture. AFT024, a mouse fetal liver stromal cell line that maintains stem cell activity in long-term culture, was subjected to SST analysis. We identified more than 60 signal sequences or transmembrane domain containing genes expressed by AFT024 cells. We compared their expression levels between AFT024 cells and BFC012 cells, a mouse fetal liver stromal cell line that was developed in the same way as for AFT024 cells but could not support HSC in long-term culture. Pleiotrophin, T16, Sca-1, deltalike and cytokine receptor like-1(CLF-1) are expressed significantly higher in AFT024 cells than in BFC012 cells. We recently employed Affymatrix genechip technology to study the interaction of HSCs and their microenvironment. In genechip experiments, Sca-1, deltalike, pleiotrophin and CLF-1 are among the most differentially expressed genes between AFT024 and BFC012 cells, while T16 was not represented on the chip. In addition, osteopontin, pigment epithelium-derived factor, proliferins, activin subunit, CXC chemokines GRO1 and LIX are more abundant in AFT024 cells than in BFC012 cells. Genechip technology was also applied to bone marrow stromal cell lines, including MS5, S17 and OP9 cells. Two murine multipotent hematopoietic cell lines, FDCP.mix and EML cells, were also analyzed. Data from these experiments are presented.
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spelling mit-1721.1/40442019-04-10T08:59:57Z Molecular Study of Interactions between Hematopoietic Stem Cells and Stromal Cells Luo, Biao Meng-Ling, Choong Heard, Amanda Li, Zhe Moore, Kateri Kaiser, Chris Lemischka, Ihor R. Yap, Miranda G.S. Lodish, Harvey F. multipotent hematopoietic stem cells hematopoietic cells Signal Sequence Trap stromal cells Multipotent hematopoietic stem cells (HSCs) are progenitors of all types of hematopoietic cells, and the efficient isolation and propagation of HSCs will significantly enhance our ability to manage many human disorders with bone marrow transplantation, stem cell transplantation and gene therapy. We employed "Signal Sequence Trap (SST)" method with yeast invertase to clone proteins on the surface of or secreted by stromal cells that enhance or inhibit the propagation of HSC’s in culture. AFT024, a mouse fetal liver stromal cell line that maintains stem cell activity in long-term culture, was subjected to SST analysis. We identified more than 60 signal sequences or transmembrane domain containing genes expressed by AFT024 cells. We compared their expression levels between AFT024 cells and BFC012 cells, a mouse fetal liver stromal cell line that was developed in the same way as for AFT024 cells but could not support HSC in long-term culture. Pleiotrophin, T16, Sca-1, deltalike and cytokine receptor like-1(CLF-1) are expressed significantly higher in AFT024 cells than in BFC012 cells. We recently employed Affymatrix genechip technology to study the interaction of HSCs and their microenvironment. In genechip experiments, Sca-1, deltalike, pleiotrophin and CLF-1 are among the most differentially expressed genes between AFT024 and BFC012 cells, while T16 was not represented on the chip. In addition, osteopontin, pigment epithelium-derived factor, proliferins, activin subunit, CXC chemokines GRO1 and LIX are more abundant in AFT024 cells than in BFC012 cells. Genechip technology was also applied to bone marrow stromal cell lines, including MS5, S17 and OP9 cells. Two murine multipotent hematopoietic cell lines, FDCP.mix and EML cells, were also analyzed. Data from these experiments are presented. Singapore-MIT Alliance (SMA) 2003-12-23T15:31:10Z 2003-12-23T15:31:10Z 2002-01 Article http://hdl.handle.net/1721.1/4044 en_US Molecular Engineering of Biological and Chemical Systems (MEBCS); 6423 bytes application/pdf application/pdf
spellingShingle multipotent hematopoietic stem cells
hematopoietic cells
Signal Sequence Trap
stromal cells
Luo, Biao
Meng-Ling, Choong
Heard, Amanda
Li, Zhe
Moore, Kateri
Kaiser, Chris
Lemischka, Ihor R.
Yap, Miranda G.S.
Lodish, Harvey F.
Molecular Study of Interactions between Hematopoietic Stem Cells and Stromal Cells
title Molecular Study of Interactions between Hematopoietic Stem Cells and Stromal Cells
title_full Molecular Study of Interactions between Hematopoietic Stem Cells and Stromal Cells
title_fullStr Molecular Study of Interactions between Hematopoietic Stem Cells and Stromal Cells
title_full_unstemmed Molecular Study of Interactions between Hematopoietic Stem Cells and Stromal Cells
title_short Molecular Study of Interactions between Hematopoietic Stem Cells and Stromal Cells
title_sort molecular study of interactions between hematopoietic stem cells and stromal cells
topic multipotent hematopoietic stem cells
hematopoietic cells
Signal Sequence Trap
stromal cells
url http://hdl.handle.net/1721.1/4044
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