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Identification of endoglin as a functional marker that defines long-term repopulating hematopoietic stem cells.


ABSTRACT: We describe a strategy to obtain highly enriched long-term repopulating (LTR) hematopoietic stem cells (HSCs) from bone marrow side-population (SP) cells by using a transgenic reporter gene driven by a stem cell enhancer. To analyze the gene-expression profile of the rare HSC population, we developed an amplification protocol termed "constant-ratio PCR," in which sample and control cDNAs are amplified in the same PCR. This protocol allowed us to identify genes differentially expressed in the enriched LTR-HSC population by oligonucleotide microarray analysis using as little as 1 ng of total RNA. Endoglin, an ancillary transforming growth factor beta receptor, was differentially expressed by the enriched HSCs. Importantly, endoglin-positive cells, which account for 20% of total SP cells, contain all the LTR-HSC activity within bone marrow SP. Our results demonstrate that endoglin, which plays important roles in angiogenesis and hematopoiesis, is a functional marker that defines LTR HSCs. Our overall strategy may be applicable for the identification of markers for other tissue-specific stem cells.

SUBMITTER: Chen CZ 

PROVIDER: S-EPMC137740 | biostudies-literature | 2002 Nov

REPOSITORIES: biostudies-literature

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Identification of endoglin as a functional marker that defines long-term repopulating hematopoietic stem cells.

Chen Chang-Zheng CZ   Li Min M   de Graaf David D   Monti Stefano S   Göttgens Berthold B   Sanchez Maria-Jose MJ   Lander Eric S ES   Golub Todd R TR   Green Anthony R AR   Lodish Harvey F HF  

Proceedings of the National Academy of Sciences of the United States of America 20021115 24


We describe a strategy to obtain highly enriched long-term repopulating (LTR) hematopoietic stem cells (HSCs) from bone marrow side-population (SP) cells by using a transgenic reporter gene driven by a stem cell enhancer. To analyze the gene-expression profile of the rare HSC population, we developed an amplification protocol termed "constant-ratio PCR," in which sample and control cDNAs are amplified in the same PCR. This protocol allowed us to identify genes differentially expressed in the enr  ...[more]

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