Thromb Haemost 2015; 114(05): 969-981
DOI: 10.1160/TH14-09-0727
Cellular Haemostasis and Platelets
Schattauer GmbH

Role of mTOR1 and mTOR2 complexes in MEG-01 cell physiology

Esther López
1   Department of Physiology (PHYCELL), University of Extremadura, Cáceres, Spain
,
Alejandro Berna-Erro
1   Department of Physiology (PHYCELL), University of Extremadura, Cáceres, Spain
,
Javier J. López
1   Department of Physiology (PHYCELL), University of Extremadura, Cáceres, Spain
,
María P. Granados
1   Department of Physiology (PHYCELL), University of Extremadura, Cáceres, Spain
,
Nuria Bermejo
2   Hematology Unit, San Pedro de Alcántara Hospital, Cáceres, Spain
,
José M. Brull
3   Blood donation centre Extremadura, Mérida, Spain
,
Ginés M. Salido
1   Department of Physiology (PHYCELL), University of Extremadura, Cáceres, Spain
,
Juan A. Rosado
1   Department of Physiology (PHYCELL), University of Extremadura, Cáceres, Spain
,
Pedro C. Redondo
1   Department of Physiology (PHYCELL), University of Extremadura, Cáceres, Spain
› Author Affiliations
Further Information

Publication History

Received: 04 September 2014

Accepted after major revision: 23 May 2015

Publication Date:
06 December 2017 (online)

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Summary

The function of the mammalian target of rapamycin (mTOR) is upregulated in response to cell stimulation with growing and differentiating factors. Active mTOR controls cell proliferation, differentiation and death. Since mTOR associates with different proteins to form two functional macromolecular complexes, we aimed to investigate the role of the mTORI and mTOR2 complexes in MEG-01 cell physiology in response to thrombopoietin (TPO). By using mTOR antagonists and overexpressing FKBP38, we have explored the role of both mTOR complexes in proliferation, apoptosis, maturation-like mechanisms, endoplasmic reticulum-stress and the intracellular location of both active mTOR complexes during MEG-01 cell stimulation with TPO. The results demonstrate that mTOR1 and mTOR2 complexes play different roles in the physiology of MEG-01 cells and in the maturation-like mechanisms; hence, these findings might help to understand the mechanism underlying generation of platelets.