NIH, National Cancer Institute, Division of Cancer Treatment and Diagnosis (DCTD) NIH - National Institutes of Health National Cancer Institute DCTD - Division of Cancer Treatment and Diagnosis

Lysis of whole blood in vitro causes DNA strand breaks in human lymphocytes.

Author(s): Narayanan S, O'Donovan M RO, Duthie S J

Publication: Mutagenesis, 2001, Vol. 16, Page 455

PubMed ID: 11682634 PubMed Review Paper? No

Purpose of Paper

To determine how storage medium (isolated or cultured lymphocytes, or whole blood) and duration influence DNA damage in lymphocytes.

Conclusion of Paper

DNA damage in lymphocytes is adversely affected by incubation with granulocytes and unidentified constituent(s) of whole blood in a time-dependent manner. Whole blood storage for 24 hours or more (at 4 degrees C or room temperature) resulted in a significant increase in DNA damage.

Studies

  1. Study Purpose

    To determine if DNA damage in lymphocytes is influenced by culture in whole blood.

    Summary of Findings:

    DNA damage was 10-fold greater in whole blood specimens compared to lymphocytes isolated from whole blood post collection.

    Biospecimens
    Preservative Types
    • None (Fresh)
    Diagnoses:
    • Not specified
    Platform:
    AnalyteTechnology Platform
    DNA Comet assay
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Biospecimen Aliquots and Components Blood and blood products Lymphocyte
    Whole blood
  2. Study Purpose

    To determine if DNA damage in lymphocytes is influenced by the storage conditions (duration and temperature) of whole blood specimens.

    Summary of Findings:

    Storage of whole blood for 24 h (at 4 degrees C or room temperature) significantly induced DNA damage, which was further elevated after 48 h in specimens stored at room temperature.

    Biospecimens
    Preservative Types
    • None (Fresh)
    Diagnoses:
    • Not specified
    Platform:
    AnalyteTechnology Platform
    DNA Comet assay
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Storage Storage temperature Room temperature
    4 degrees C
    Storage Storage duration 0 h
    24 h
    48 h
  3. Study Purpose

    To assess comparative differences in DNA damage among specimens with different levels of red blood cell contamination risk: 1) lymphocytes grown in mononuclear culture, 2) lymphocytes isolated from whole blood post collection, and 3) lymphocytes cultured in whole blood.

    Summary of Findings:

    While lymphocytes grown in mononuclear cell culture and those isolated from whole blood had comparable levels of DNA damage on days 0 and 1, the latter displayed significantly higher levels of DNA damage on day 2. DNA damage in lymphocytes isolated from whole blood and those cultured in whole blood increased as a function of time. Lymphocytes cultured in granulocyte depleted blood displayed intermediate levels of DNA damage in comparison to those grown in mononuclear culture or whole blood, indicating that a whole blood constituent in addition to granulocytes influences lymphocyte DNA damage.

    Biospecimens
    Preservative Types
    • None (Fresh)
    Diagnoses:
    • Not specified
    Platform:
    AnalyteTechnology Platform
    Cell count/volume Flow cytometry
    DNA Comet assay
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Storage Storage duration 0 days
    1 day
    2 days
    3 days
    4 days
    7 days
    Biospecimen Aliquots and Components Blood and blood products Lymphocytes
    Whole blood

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