1. Academic Validation
  2. Improvement of platelet preservation by inhibition of TRPC6

Improvement of platelet preservation by inhibition of TRPC6

  • Transfus Med. 2023 Feb 6. doi: 10.1111/tme.12955.
Yuanjia Tan 1 2 Wei Lu 3 Xiaomei Yi 3 Huili Cai 4 Yurong Yuan 3 Shizhong Zhang 1 2
Affiliations

Affiliations

  • 1 Third-Grade Pharmacological Laboratory on Traditional Chinese Medicine, China Three Gorges University, Yichang, China.
  • 2 Department of Physiology, Medical College of China Three Gorges University, Yichang, China.
  • 3 Office, The Blood Bank Center of Yichang City, Yichang, China.
  • 4 Department of Hematology, Yichang Central People' Hospital, The First College of Clinical Medical Science, China Three Gorges University, Yichang, China.
Abstract

Background: The preservation of platelets (PLTs) by room temperature (RT) oscillation limits their shelf life to between 4 and 7 days because of the decrease in PLT function. TRPC6 is a non-selective mechanically sensitive cation channel that has been shown to mediate Ca2+ signalling, implying a role in PLT activation during preservation by RT oscillation.

Objectives: This study was designed to investigate whether inhibition of TRPC6 can improve the RT preservation of PLTs and the possible underlying mechanism.

Methods: Human PLTs from whole blood were stored at 22 ± 2°C with oscillation in plasma or M-sol (mixture of solutions). BI-749327, a specific TRPC6 inhibitor, was administered throughout the preservation period. PLT distribution width (PDW), mean platelet volume (MPV), maximum platelet aggregation rate (MAR) and average aggregation rate (AAR) were measured. The MTT method was used to assess the relative viability of PLTs. Flow cytometry was used to measure the changes of Ca2+ concentration in PLTs and phosphatidylserine (PS) exposure on the PLT surface, and western blotting was used to assess the expression changes of platelet TRPC6 and CD62P proteins.

Results: Compared with the control group, inhibition of TRPC6 with BI-749327 significantly reduced the PDW, MPV and Ca2+ concentration, the MAR and AAR were significantly increased, the expression of TRPC6 and CD62P protein was significantly down-regulated in PLTs, and the PS exposure was significantly reduced on the PLT surface. However, these effects were all reversed by activation of TRPC6.

Conclusion: Inhibition of TRPC6 improves the quality of PLT preservation by inhibiting the Ca2+ signal mediated by TRPC6.

Keywords

TRPC6; platelet activation; platelet preservation.

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