Literature DB >> 11204566

Expression of translation initiation factors elF-4E and elF-2alpha and a potential physiologic role of continuous protein synthesis in human platelets.

I B Rosenwald1, L Pechet, A Han, L Lu, G Pihan, B Woda, J J Chen, I Szymanski.   

Abstract

It is generally believed that platelets do not have a functionally significant protein synthetic machinery. However, our analysis demonstrated that normal bone marrow megakaryocytes express high levels of translation initiation factors eIF-4E and eIF-2alpha and the expression of these protein synthesis initiation factors is continued in platelets (as determined by immunohistochemistry and Western blot analysis). Both eIF-4E and eIF-2alpha are key regulators of protein synthesis. The eIF-4E is a rate-limiting part of a multisubunit complex, eIF-4F, that binds to the 5' cap structure present in virtually all eukaryotic mRNAs, and carries out transfer of mRNAs to ribosomes for translation. Translation initiation factor eIF-2alpha is also a rate-limiting protein which associates with two other proteins to form an eIF-2 initiation factor complex responsible for the transfer of initiator methionyl-tRNA to the 40S ribosomal subunit. We confirm that expression of eIF-4E and eIF-2alpha is biologically relevant in that platelets continue protein synthesis, albeit at a 16 times lower rate than WBC (as determined by 35S-labeled amino acid incorporation, SDS-PAGE and scintillation counting). Finally, we determined that protein synthesis inhibitors (puromycin and emetine) attenuate the platelet aggregation response to a combination of ADP and epinephrine, but potentiate the response to collagen. Our data are consistent with the existence of different signal transducing pathways mediating the response to ADP/epinephrine and collagen. We suggest that the ADP/epinephrine response is positively affected by continuously synthesized proteins, while the response to collagen is modulated by continuously produced inhibitory proteins. Taken together, our results suggest that continuous protein synthesis is important for platelet function and its role in platelet physiology and pathophysiology deserves further study.

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Year:  2001        PMID: 11204566

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  13 in total

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Review 4.  Signal-dependent protein synthesis by activated platelets: new pathways to altered phenotype and function.

Authors:  Guy A Zimmerman; Andrew S Weyrich
Journal:  Arterioscler Thromb Vasc Biol       Date:  2008-03       Impact factor: 8.311

Review 5.  Protein synthesis by platelets: historical and new perspectives.

Authors:  A S Weyrich; H Schwertz; L W Kraiss; G A Zimmerman
Journal:  J Thromb Haemost       Date:  2008-10-29       Impact factor: 5.824

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Review 7.  Targeting Mnks for cancer therapy.

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8.  Regulation of the mTOR-Rac1 axis in platelet function.

Authors:  Joseph E Aslan; Owen J T McCarty
Journal:  Small GTPases       Date:  2012 Jan-Mar

9.  Phosphorylated Mnk1 and eIF4E are associated with lymph node metastasis and poor prognosis of nasopharyngeal carcinoma.

Authors:  Jun Zheng; Jiao Li; Lina Xu; Guiyuan Xie; Qiuyuan Wen; Jiadi Luo; Duo Li; Donghai Huang; Songqing Fan
Journal:  PLoS One       Date:  2014-02-14       Impact factor: 3.240

10.  Time-Dependent Decay of mRNA and Ribosomal RNA during Platelet Aging and Its Correlation with Translation Activity.

Authors:  Catherine Angénieux; Blandine Maître; Anita Eckly; François Lanza; Christian Gachet; Henri de la Salle
Journal:  PLoS One       Date:  2016-01-25       Impact factor: 3.240

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