Megakaryocyte maturation involves activation of the adaptive unfolded protein response

Author:

Faiz Mifra1ORCID,Kalev‐Zylinska Maggie L.2ORCID,Dunstan‐Harrison Caitlin1ORCID,Singleton Dean C.3ORCID,Hay Michael P.3ORCID,Ledgerwood Elizabeth C.1ORCID

Affiliation:

1. Department of Biochemistry School of Biomedical Sciences, University of Otago Dunedin New Zealand

2. Blood and Cancer Biology Laboratory, Department of Molecular Medicine & Pathology Faculty of Medical and Health Sciences, The University of Auckland Auckland New Zealand

3. Auckland Cancer Society Research Centre Faculty of Medical and Health Sciences, The University of Auckland Auckland New Zealand

Abstract

AbstractEndoplasmic reticulum stress triggers the unfolded protein response (UPR) to promote cell survival or apoptosis. Transient endoplasmic reticulum stress activation has been reported to trigger megakaryocyte production, and UPR activation has been reported as a feature of megakaryocytic cancers. However, the role of UPR signaling in megakaryocyte biology is not fully understood. We studied the involvement of UPR in human megakaryocytic differentiation using PMA (phorbol 12‐myristate 13‐acetate)‐induced maturation of megakaryoblastic cell lines and thrombopoietin‐induced differentiation of human peripheral blood‐derived progenitors. Our results demonstrate that an adaptive UPR is a feature of megakaryocytic differentiation and that this response is not associated with ER stress‐induced apoptosis. Differentiation did not alter the response to the canonical endoplasmic reticulum stressors DTT or thapsigargin. However, thapsigargin, but not DTT, inhibited differentiation, consistent with the involvement of Ca2+ signaling in megakaryocyte differentiation.

Funder

Leukaemia and Blood Cancer New Zealand

University of Otago

Auckland Medical Research Foundation

Publisher

Wiley

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