Abstract

Previous investigations have indicated that RNAs are mostly present in the minor population of the youngest platelets, whereas translation in platelets could be biologically important. To attempt to solve this paradox, we studied changes in the RNA content of reticulated platelets, i.e., young cells brightly stained by thiazole orange (TObright), a fluorescent probe for RNAs. We provoked in mice strong thrombocytopenia followed by dramatic thrombocytosis characterized by a short period with a vast majority of reticulated platelets. During thrombocytosis, the TObright platelet count rapidly reached a maximum, after which TOdim platelets accumulated, suggesting that most of the former were converted into the latter within 12 h. Experiments on platelets, freshly isolated or incubated ex vivo at 37°C, indicated that their “RNA content”, here corresponding to the amounts of extracted RNA, and the percentage of TObright platelets were positively correlated. The “RNA Content” normalized to the number of platelets could be 20 to 40 fold higher when 80–90% of the cells were reticulated (20–40 fg/platelet), than when only 5–10% of control cells were TObright (less than 1fg/platelet). TObright platelets, incubated ex vivo at 37°C or transfused into mice, became TOdim within 24 h. Ex vivo at 37°C, platelets lost about half of their ribosomal and beta actin RNAs within 6 hours, and more than 98% of them after 24 hours. Accordingly, fluorescence in situ hybridization techniques confirmed the presence of beta actin mRNAs in most reticulated-enriched platelets, but detected them in only a minor subset of control platelets. In vitro, constitutive translation decreased considerably within less than 6 hours, questioning how protein synthesis in platelets, especially in non-reticulated ones, could have a biological function in vivo. Nevertheless, constitutive transient translation in young platelets under pathological conditions characterized by a dramatic increase in circulating reticulated platelets could deserve to be investigated.

Highlights

  • The major primary hemostatic functions of blood platelets (PLTs) imply a series of rapid signal transduction events generally completed within a few seconds or minutes [1]

  • We studied the time-dependent changes of the “RNA content” of PLTs, the integrity of their ribosomal RNA (rRNA), the life span of beta actin mRNA in platelets placed in ex vivo conditions and, the constitutive biosynthetic activity in PLTs

  • Since the life span of mouse PLTs is about 5 days [15], this time course indicated that DT killed maturing MKs, while PLT rebound occurred after the restoration of full MK differentiation

Read more

Summary

Introduction

The major primary hemostatic functions of blood platelets (PLTs) imply a series of rapid signal transduction events generally completed within a few seconds or minutes [1]. The experimental evidence that translation can occur in PLTs challenged this view and incites one to better characterize their RNA content In this objective, we studied the time-dependent changes of the “RNA content” of PLTs (defined as the RNA molecules extracted from PLTs), the integrity of their rRNA, the life span of beta actin mRNA in platelets placed in ex vivo conditions and, the constitutive biosynthetic activity in PLTs. Steady state conditions were compared with experimental conditions characterized by the transient presence of a vast majority of retPLTs. Our results were correlated with previously published genetic studies of PLTs to assess the biological relevance of the deduced relative amounts of specific mRNAs in PLTs. Our experimental system provides a unique means of investigating in vivo the functional characteristics of retPLTs

Results
Discussion
Methods
Ethic statement
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call