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  1. Article ; Online: Endothelial cell high-enrichment from endovascular biopsy sample by laser capture microdissection and fluorescence activated cell sorting.

    Sun, Zhengda / Su, Hua / Long, Brian / Sinclair, Elizabeth / Hetts, Steven W / Higashida, Randall T / Dowd, Christopher F / Halbach, Van V / Cooke, Daniel L

    Journal of biotechnology

    2014  Volume 192 Pt A, Page(s) 34–39

    Abstract: ... fluorescence activated cell sorting (FACS) technique, and addressed the feasibility of using these enriched ECs for downstream ... enrichment from conventional guide wires by laser capture microdissection (LCM) and ... by the lack of an effective method of endothelial cell (EC) enrichment. We optimized the EC yield and ...

    Abstract Background and purpose: Endovascular sampling and characterization from patients can provide very useful information about the pathogenesis of different vascular diseases, but it has been limited by the lack of an effective method of endothelial cell (EC) enrichment. We optimized the EC yield and enrichment from conventional guide wires by laser capture microdissection (LCM) and fluorescence activated cell sorting (FACS) technique, and addressed the feasibility of using these enriched ECs for downstream gene expression detection.
    Methods: Iliac artery endovascular samples from 10 patients undergoing routine catheter angiography were collected using conventional 0.038 in. J-shape guide wires. Each of these samples was equally divided into two parts, which were respectively used for EC enrichment by immunocytochemistry-coupled LCM or multiple color FACS. After RNA extraction and reverse transcription, the amplified cDNA was used for quantitative polymerase chain reaction (qPCR).
    Results: Fixed ECs, with positive CD31 or vWF fluorescent signal and endothelial like nucleus, were successfully separated by LCM and live single ECs were sorted on FACS by a seven color staining panel. EC yields by LCM and FACS were 51 ± 22 and 149 ± 56 respectively (P < 0.001). The minimum number of fixed ECs from ICC-coupled LCM for acceptable qPCR results of endothelial marker genes was 30, while acceptable qPCR results as enriched by FACS were attainable from a single live EC.
    Conclusion: Both LCM and FACS can be used to enrich ECs from conventional guide wires and the enriched ECs can be used for downstream gene expression detection. FACS generated a higher EC yield and the sorted live ECs may be used for single cell gene expression detection.
    MeSH term(s) Biopsy ; DNA, Complementary/genetics ; Endothelial Cells/cytology ; Flow Cytometry ; Gene Expression ; Humans ; Iliac Artery/cytology ; Iliac Artery/diagnostic imaging ; Iliac Artery/surgery ; Laser Capture Microdissection ; RNA/genetics ; Radiography ; Real-Time Polymerase Chain Reaction
    Chemical Substances DNA, Complementary ; RNA (63231-63-0)
    Language English
    Publishing date 2014-12-20
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 843647-2
    ISSN 1873-4863 ; 0168-1656 ; 1389-0352
    ISSN (online) 1873-4863
    ISSN 0168-1656 ; 1389-0352
    DOI 10.1016/j.jbiotec.2014.07.434
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Endothelial cell high-enrichment from endovascular biopsy sample by laser capture microdissection and fluorescence activated cell sorting

    Sun, Zhengda / Brian Long / Christopher F. Dowd / Daniel L. Cooke / Elizabeth Sinclair / Hua Su / Randall T. Higashida / Steven W. Hetts / Van V. Halbach

    Journal of biotechnology. 2014 Dec. 20, v. 192

    2014  

    Abstract: ... by laser capture microdissection (LCM) and fluorescence activated cell sorting (FACS) technique, and addressed the feasibility ... of endothelial cell (EC) enrichment. We optimized the EC yield and enrichment from conventional guide wires ... of using these enriched ECs for downstream gene expression detection.Iliac artery endovascular samples ...

    Abstract Endovascular sampling and characterization from patients can provide very useful information about the pathogenesis of different vascular diseases, but it has been limited by the lack of an effective method of endothelial cell (EC) enrichment. We optimized the EC yield and enrichment from conventional guide wires by laser capture microdissection (LCM) and fluorescence activated cell sorting (FACS) technique, and addressed the feasibility of using these enriched ECs for downstream gene expression detection.Iliac artery endovascular samples from 10 patients undergoing routine catheter angiography were collected using conventional 0.038in. J-shape guide wires. Each of these samples was equally divided into two parts, which were respectively used for EC enrichment by immunocytochemistry-coupled LCM or multiple color FACS. After RNA extraction and reverse transcription, the amplified cDNA was used for quantitative polymerase chain reaction (qPCR).Fixed ECs, with positive CD31 or vWF fluorescent signal and endothelial like nucleus, were successfully separated by LCM and live single ECs were sorted on FACS by a seven color staining panel. EC yields by LCM and FACS were 51±22 and 149±56 respectively (P<0.001). The minimum number of fixed ECs from ICC-coupled LCM for acceptable qPCR results of endothelial marker genes was 30, while acceptable qPCR results as enriched by FACS were attainable from a single live EC.Both LCM and FACS can be used to enrich ECs from conventional guide wires and the enriched ECs can be used for downstream gene expression detection. FACS generated a higher EC yield and the sorted live ECs may be used for single cell gene expression detection.
    Keywords biopsy ; catheters ; color ; complementary DNA ; endothelial cells ; flow cytometry ; fluorescence ; gene expression ; genetic markers ; pathogenesis ; patients ; quantitative polymerase chain reaction ; reverse transcription ; RNA ; staining ; vascular diseases
    Language English
    Dates of publication 2014-1220
    Size p. 34-39.
    Publishing place Elsevier B.V.
    Document type Article
    ZDB-ID 843647-2
    ISSN 1873-4863 ; 0168-1656 ; 1389-0352
    ISSN (online) 1873-4863
    ISSN 0168-1656 ; 1389-0352
    DOI 10.1016/j.jbiotec.2014.07.434
    Database NAL-Catalogue (AGRICOLA)

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