Brain-specific 1B promoter of FGF1 gene facilitates the isolation of neural stem/progenitor cells with self-renewal and multipotent capacities

Yi Chao Hsu, Don Ching Lee, Su Liang Chen, Wei Chih Liao, Jia Wei Lin, Wen Ta Chiu, Ing Ming Chiu

研究成果: 雜誌貢獻文章

34 引文 (Scopus)

摘要

Fibroblast growth factor 1 (FGF1) has been shown to maintain proliferation and self-renewal capacities of neural stem/progenitor cells (NSPCs) in vitro. We have previously identified FGF1B as the major transcript of FGF1 gene expressed exclusively in brain areas that are known to be abundant for NSPCs in vivo. The 540-bp (-540 to +31) sequence upstream of the 1B transcription start site (F1B) is sufficient to drive the expression of a heterologous luciferase reporter in cultured cells. In this study, we report a direct genetic and functional approach to isolate F1B(+) NSPCs using green fluorescent protein (GFP) reporter gene under the control of human F1B promoter. The F1B-GFP reporter could facilitate the isolation of NSPCs with self-renewal and multipotent capacities from human glioblastoma tissues, developing or adult mouse brains by fluorescence-activated cell sorting. Future work elucidating the mechanisms that control FGF1B expression will help to identify new NSPC-related genes.
原文英語
頁(從 - 到)302-314
頁數13
期刊Developmental Dynamics
238
發行號2
DOIs
出版狀態已發佈 - 二月 2009

指紋

Fibroblast Growth Factor 1
Neural Stem Cells
Stem Cells
Brain
Genes
Green Fluorescent Proteins
Transcription Initiation Site
Glioblastoma
Luciferases
Reporter Genes
Cultured Cells
Flow Cytometry
Cell Self Renewal

ASJC Scopus subject areas

  • Developmental Biology

引用此文

Brain-specific 1B promoter of FGF1 gene facilitates the isolation of neural stem/progenitor cells with self-renewal and multipotent capacities. / Hsu, Yi Chao; Lee, Don Ching; Chen, Su Liang; Liao, Wei Chih; Lin, Jia Wei; Chiu, Wen Ta; Chiu, Ing Ming.

於: Developmental Dynamics, 卷 238, 編號 2, 02.2009, p. 302-314.

研究成果: 雜誌貢獻文章

Hsu, Yi Chao ; Lee, Don Ching ; Chen, Su Liang ; Liao, Wei Chih ; Lin, Jia Wei ; Chiu, Wen Ta ; Chiu, Ing Ming. / Brain-specific 1B promoter of FGF1 gene facilitates the isolation of neural stem/progenitor cells with self-renewal and multipotent capacities. 於: Developmental Dynamics. 2009 ; 卷 238, 編號 2. 頁 302-314.
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abstract = "Fibroblast growth factor 1 (FGF1) has been shown to maintain proliferation and self-renewal capacities of neural stem/progenitor cells (NSPCs) in vitro. We have previously identified FGF1B as the major transcript of FGF1 gene expressed exclusively in brain areas that are known to be abundant for NSPCs in vivo. The 540-bp (-540 to +31) sequence upstream of the 1B transcription start site (F1B) is sufficient to drive the expression of a heterologous luciferase reporter in cultured cells. In this study, we report a direct genetic and functional approach to isolate F1B(+) NSPCs using green fluorescent protein (GFP) reporter gene under the control of human F1B promoter. The F1B-GFP reporter could facilitate the isolation of NSPCs with self-renewal and multipotent capacities from human glioblastoma tissues, developing or adult mouse brains by fluorescence-activated cell sorting. Future work elucidating the mechanisms that control FGF1B expression will help to identify new NSPC-related genes.",
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AU - Liao, Wei Chih

AU - Lin, Jia Wei

AU - Chiu, Wen Ta

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AB - Fibroblast growth factor 1 (FGF1) has been shown to maintain proliferation and self-renewal capacities of neural stem/progenitor cells (NSPCs) in vitro. We have previously identified FGF1B as the major transcript of FGF1 gene expressed exclusively in brain areas that are known to be abundant for NSPCs in vivo. The 540-bp (-540 to +31) sequence upstream of the 1B transcription start site (F1B) is sufficient to drive the expression of a heterologous luciferase reporter in cultured cells. In this study, we report a direct genetic and functional approach to isolate F1B(+) NSPCs using green fluorescent protein (GFP) reporter gene under the control of human F1B promoter. The F1B-GFP reporter could facilitate the isolation of NSPCs with self-renewal and multipotent capacities from human glioblastoma tissues, developing or adult mouse brains by fluorescence-activated cell sorting. Future work elucidating the mechanisms that control FGF1B expression will help to identify new NSPC-related genes.

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