Department of Clinical Biochemistry, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran.
Transfus Clin Biol. 2024 May;31(2):87-94. doi: 10.1016/j.tracli.2024.01.007. Epub 2024 Jan 22.
Micro RNAs are known as the main regulator of messenger RNA translation in platelets and have a vital role in process of apoptosis during platelet storage. Our pervious study revealed that the expression of miR-145 and miR-326 changed significantly in platelets under maintenance conditions. This study aimed to evaluate the effect of L-carnitine (LC) as an additive to augment platelet quality by changing the microRNA expression.
We used ten platelet concentrate (PC) bags and divided each into two equal parts, LC- treated, and LC free PC. The expression of miR-145 and miR-326 were determined using real-time PCR. Moreover, we measured platelet count, platelet aggregation, platelet viability, and lactate dehydrogenase activity in all samples.
The miR-326 expression significantly increased during platelet storage with mean fold changes of 3.2 for the control and 2.5 for LC- treated PC. The mean fold changes in miR-145 expression was less in the control PC (0.52) compared to the LC- treated PC (0.79). Increased levels of platelet count, platelet aggregation, and platelet viability were found in the LC-treated compared to the untreated PC.
LC has a protective effect on platelet apoptosis, reduces the expression of apoptotic microRNA, and prevents the reduction of anti-apoptotic microRNA.
微 RNA 被认为是血小板中信使 RNA 翻译的主要调节因子,在血小板储存过程中的凋亡过程中起着至关重要的作用。我们之前的研究表明,miR-145 和 miR-326 的表达在维持条件下的血小板中发生了显著变化。本研究旨在评估左旋肉碱 (LC) 作为添加剂通过改变微 RNA 表达来提高血小板质量的效果。
我们使用了 10 个血小板浓缩物 (PC) 袋,并将每个袋分成两等份,分别为 LC 处理和无 LC 的 PC。使用实时 PCR 测定 miR-145 和 miR-326 的表达。此外,我们测量了所有样本中的血小板计数、血小板聚集、血小板活力和乳酸脱氢酶活性。
miR-326 在血小板储存过程中的表达显著增加,对照组的平均倍数变化为 3.2,LC 处理组为 2.5。对照组 PC 中 miR-145 表达的平均倍数变化(0.52)低于 LC 处理组(0.79)。LC 处理组的血小板计数、血小板聚集和血小板活力水平均高于未处理组。
LC 对血小板凋亡具有保护作用,降低了凋亡微 RNA 的表达,并防止了抗凋亡微 RNA 的减少。