MiR-181a Reduces Platelet Activation via the Inhibition of Endogenous RAP1B

(E-pub Ahead of Print)

Author(s): Neetu Dahiya, Chintamani D. Atreya*.

Journal Name: MicroRNA

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Abstract:

Aim: Since RAP1B is critical for platelet functions including hemostasis, this study was conducted to identify RAP1B regulating microRNAs (miRNAs) in ex vivo stored platelets.

Background: Previous studies with platelets identified factors affecting RAP1B activity but regulatory miRNAs that affect RAP1B protein expression has not been reported.

Objective: To understand the functional significance of miRNA mediated regulation of RAP1B in stored platelets, using microRNA, miR-181a as an example.

Methods: A tagged RNA affinity approach (MS2-TRAP) was employed to identify miRNAs that bound to the 3` untranslated region (3`UTR) of the RAP1B mRNA first in HeLa cells as an assay system and subsequently the mRNA 3’UTR:miRNA interactions were verified in platelets through ectopic expression of miR-181a mimic and appropriate controls. Interaction of such miRNAs with RAP1B mRNA were also validated by qRT-PCR and Western analysis.

Results: Sixty-two miRNAs emerged through MS2 assay were then compared with already known 171 platelet abundant miRNAs to identify a common set of miRNAs. This analysis yielded six miRNAs (miR-30e, miR-155, miR-181a, miR-206, miR-208a and miR-454), which are also predicted to target RAP1B mRNA. From this pool miR-181a was selected for further study since RAP1B harbors two binding sites for miR-181a in its 3´UTR. Ectopic expression of miR-181a mimic in platelets resulted in lowering the endogenous RAP1B at both the mRNA and protein levels. Further, miR-181a ectopic expression reduced the surface expression of platelet activation marker, P-selectin.

Conclusion: MicroRNA-181a can target RAP1B and this interaction has the potential to regulate platelet activation during storage.

Keywords: microRNA, RAP1, platelets, miR-181, platelet activation, MS2-TRAPmicroRNA, RAP1, platelets, miR-181, platelet activation, MS2-TRAP

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Article Details

(E-pub Ahead of Print)
DOI: 10.2174/2211536608666191026120515

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