4.5 Article

The impact of pre-freezing storage time and temperature on gene expression of blood collected in EDTA tubes

Journal

MOLECULAR BIOLOGY REPORTS
Volume 49, Issue 6, Pages 4709-4718

Publisher

SPRINGER
DOI: 10.1007/s11033-022-07320-5

Keywords

EDTA tubes; Ex vivo incubation; Blood; PBMC; RNA yield; RNA quality; Gene expression

Funding

  1. FISM-Fondazione Italiana Sclerosi Multipla-cod [2020/S/5]

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This study evaluated the influence of storage time and temperature on RNA from peripheral blood mononuclear cells (PBMCs). The results showed that time and temperature had minimal impact on RNA yield, quality, and integrity. B2M was the most stable housekeeping gene, while other target genes were more influenced by storing time, especially at low temperature. Pre-analytical processing of blood collected in EDTA tubes has a significant impact on transcript expression, particularly for genes related to inflammation. Standardized procedures for blood handling are necessary for obtaining reliable results.
Background Blood is a common source of RNA for gene expression studies. However, it is known to be vulnerable to pre-analytical variables. Although RNA stabilization systems have been shown to reduce such influence, traditional EDTA tubes are still widely used since they are less expensive and enable to study specific leukocyte populations. This study aimed to assess the influence of storage time and temperature between blood sampling and handling on RNA from peripheral blood mononuclear cells (PBMCs). Methods and results Nine blood samples were collected in EDTA tubes from 10 healthy donors. One tube from each donor was immediately processed for PBMC isolation, while the others were first incubated at either 4 degrees Celsius (degrees C) or room temperature for 2, 4, 6 and 24 h. RNA yield and quality and the expression level of fourt housekeeping (B2M, CASC3, GAPDH, HPRT1) and 8 target genes (CD14, CD19, CD20, IL10, MxA, TNF, TNFAIP3, NR4A2) were compared between samples. RNA yield, quality and integrity did not vary significantly with time and temperature. B2M was the most stable housekeeping gene, while the others were increasingly influenced by storing time, especially at 4 degrees C. Even when normalized to B2M, the expression level of some target genes, particularly TNFAIP3 and NR4A2, was highly affected by delays in blood processing at either temperature, already from 2 h. Conclusion Pre-analytical processing has a great impact on transcript expression from blood collected in EDTA tubes, especially on genes related to inflammation. Standardized procedure of blood handling are needed to obtain reliable results.

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