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Routine Screening Method for Microparticles in Platelet Transfusions
Published on: January 31, 2018
Cold storage conditions modify microRNA expressions for platelet transfusion
Nobuhiro Mukai1, Yoshinobu Nakayama1,2, Sachiyo Ishi1
1Department of Anesthesiology and Critical Care, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Abstract:
MicroRNAs (miRNAs) are small RNA molecules that modulate gene and protein expression in hematopoiesis. Platelets are known to contain a fully functional miRNA machinery. While platelets used for transfusion are normally stored at room temperature, recent evidence suggests more favorable effects under a cold-storage condition, including higher adhesion and aggregation properties. Thus, we sought to determine whether functional differences in platelets are associated with the differential profiling of platelet miRNA expressions. To obtain the miRNA expression profile, next-generation sequencing was performed on human platelets obtained from 10 healthy subjects. The miRNAs were quantified after being stored in three different conditions: 1) baseline (before storage), 2) stored at 22°C with agitation for 72 h, and 3) stored at 4°C for 72 h. Following the identification of miRNAs by sequencing, the results were validated at the level of mature miRNAs from 18 healthy subjects, by using quantitative polymerase chain reaction (qPCR). Differential expression was observed for 125 miRNAs that were stored at 4°C and 9 miRNAs stored at 22°C as compared to the baseline. The validation study by qPCR confirmed that storage at 4°C increased the expression levels (fold change 95% CI) of mir-20a-5p (1.87, p<0.0001), mir-10a-3p (1.88, p<0.0001), mir-16-2-3p (1.54, p<0.01), and mir-223-5p (1.38, p<0.05), compared with those of the samples stored at 22°C. These results show that miRNAs correlate with platelet quality under specific storage conditions. The data indicate that miRNAs could be potentially used as biomarkers of platelet quality.
Insights
Cold storage of platelets significantly alters microRNA (miRNA) profiles, with specific miRNAs increasing in expression. These findings suggest miRNAs can serve as biomarkers for assessing platelet quality during storage.
Area of Science:
- Hematology
- Molecular Biology
- Biochemistry
Background:
- MicroRNAs (miRNAs) are key regulators of gene expression in hematopoiesis.
- Platelets possess a complete miRNA machinery and their storage conditions impact function.
- Cold storage may enhance platelet adhesion and aggregation compared to room temperature storage.
Purpose of the Study:
- To investigate the association between platelet storage conditions and differential miRNA expression profiles.
- To determine if miRNA expression can serve as a biomarker for platelet quality.
Main Methods:
- Next-generation sequencing was used to profile miRNAs in human platelets from 10 healthy subjects.
- Platelets were stored at baseline, 22°C, and 4°C for 72 hours.
- Quantitative polymerase chain reaction (qPCR) validated miRNA expression changes in 18 healthy subjects.
Main Results:
- Storage at 4°C led to differential expression of 125 miRNAs compared to baseline.
- Storage at 22°C resulted in differential expression of 9 miRNAs compared to baseline.
- qPCR confirmed increased expression of specific miRNAs (mir-20a-5p, mir-10a-3p, mir-16-2-3p, mir-223-5p) at 4°C versus 22°C.
Conclusions:
- Platelet miRNA expression profiles are significantly altered by storage temperature.
- Specific miRNAs correlate with platelet quality under different storage conditions.
- miRNAs show potential as biomarkers for evaluating platelet quality.
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