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A histological survey of green fluorescent protein expression in 'green' mice: implications for stem cell research.

A histological survey of green fluorescent protein expression in 'green' mice: implications for stem cell research. Research Abstract Details 

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  • A histological survey of green fluorescent protein expression in 'green' mice: implications for stem cell research. Abstract Text:

    sandra a biankinSandra A Biankin,michael i collectorMichael I Collector,andrew v biankinAndrew V Biankin,lindsey j brownLindsey J Brown,wolfram kleebergerWolfram Kleeberger,wendy l devereuxWendy L Devereux,cynthia a zahnowCynthia A Zahnow,stephen b baylinStephen B Baylin,d neil watkinsD Neil Watkins,saul j sharkisSaul J Sharkis,steven d leachSteven D Leach,

    AIMS: The transgenic enhanced green fluorescent protein (EGFP) expressing 'green' mouse (C57BL/6-TgN(ACTbEGFP)1Osb) is a widely used tool in stem cell research, where the ubiquitous nature of EGFP expression is critical to track the fate of single or small groups of transplanted haematopoietic stem cells (HSC). Our aim was to investigate this assumed ubiquitous expression by performing a detailed histological survey of EGFP expression in these mice. METHODS: Fluorescent microscopy of frozen tissue sections was used to perform a detailed histological survey of the pattern of EGFP expression in these mice. Flow cytometry was also used to determine the expression pattern in blood and bone marrow. RESULTS: Three patterns of EGFP expression were noted. In most tissues there was an apparently stochastic variegation of the transgene, with individual cell types demonstrating highly variable rates of EGFP expression. Certain specific cell types such as pancreatic ductal epithelium, cerebral cortical neurones and glial cells and glomerular mesangial cells consistently lacked EGFP expression, while others, including pancreatic islet cells, expressed EGFP only at extremely low levels, barely distinguishable from background. Lastly, in the colon and stomach the pattern of EGFP expression was suggestive of clonal inactivation. Only cardiac and skeletal muscle showed near ubiquitous expression. CONCLUSIONS: These findings raise questions regarding the 'ubiquitous' expression of EGFP in these transgenic mice and suggest caution in relying overly on EGFP alone as an infallible marker of donor cell origin.

    A histological survey of green fluorescent protein expression in 'green' mice: implications for stem cell research. Publishing Authors By Initials

    sa biankinSA Biankin,mi collectorMI Collector,av biankinAV Biankin,lj brownLJ Brown,w kleebergerW Kleeberger,wl devereuxWL Devereux,ca zahnowCA Zahnow,sb baylinSB Baylin,dn watkinsDN Watkins,sj sharkisSJ Sharkis,sd leachSD Leach,

    For similar cells: stem cells research abstracts see: cells: stem cells research

    PUBMED ID PMID:

    MEDLINE DATE:

    A histological survey of green fluorescent protein expression in 'green' mice: implications for stem cell research. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Pathology

    VOLUME: 39

    Page Numbers: 247-51

    Journal Abbreviation:

    ISSN: 0031-3025

    DAY: 3

    MONTH: Apr

    YEAR: 2007

    A histological survey of green fluorescent protein expression in 'green' mice: implications for stem cell research. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 175411

    A histological survey of green fluorescent protein expression in 'green' mice: implications for stem cell research. Keywords Mesh Terms:

    KEYWORDS: Stem Cells

    MESH TERMS: genetics

    Chemical & Substance for Abstract: A histological survey of green fluorescent protein expression in 'green' mice: implications for stem cell research. Information

    Substance Name: Green Fluorescent Proteins

    Registry Number: 147336-22-9

    Grant and Affiliation Information for A histological survey of green fluorescent protein expression in 'green' mice: implications for stem cell research.

    AFFILIATION: Epithelial Stem Cell Working Group, Department of Surgery, Sidney Kimmel Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, USA. s.biankin@garvan.org.au

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NHLBI

    GRANT: HL-54330

    ACRONYM: HL

    MEDLINETA: Pathology

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