Shared and Distinctive Ultrastructural Abnormalities Expressed by Megakaryocytes in Bone Marrow and Spleen From Patients With Myelofibrosis.

cell metabolism megakaryocytes myelofibrosis myeloproliferative neoplasms ultrastructural analyses

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2020
Historique:
received: 17 07 2020
accepted: 19 10 2020
entrez: 14 12 2020
pubmed: 15 12 2020
medline: 15 12 2020
Statut: epublish

Résumé

Numerous studies have documented ultrastructural abnormalities in malignant megakaryocytes from bone marrow (BM) of myelofibrosis patients but the morphology of these cells in spleen, an important extramedullary site in this disease, was not investigated as yet. By transmission-electron microscopy, we compared the ultrastructural features of megakaryocytes from BM and spleen of myelofibrosis patients and healthy controls. The number of megakaryocytes was markedly increased in both BM and spleen. However, while most of BM megakaryocytes are immature, those from spleen appear mature with well-developed demarcation membrane systems (DMS) and platelet territories and are surrounded by platelets. In BM megakaryocytes, paucity of DMS is associated with plasma (thick with protrusions) and nuclear (dilated with large pores) membrane abnormalities and presence of numerous glycosomes, suggesting a skewed metabolism toward insoluble polyglucosan accumulation. By contrast, the membranes of the megakaryocytes from the spleen were normal but these cells show mitochondria with reduced crests, suggesting deficient aerobic energy-metabolism. These distinctive morphological features suggest that malignant megakaryocytes from BM and spleen express distinctive metabolic impairments that may play different roles in the pathogenesis of myelofibrosis.

Identifiants

pubmed: 33312951
doi: 10.3389/fonc.2020.584541
pmc: PMC7701330
doi:

Types de publication

Journal Article

Langues

eng

Pagination

584541

Subventions

Organisme : NCI NIH HHS
ID : P01 CA108671
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL134684
Pays : United States

Informations de copyright

Copyright © 2020 Zingariello, Rosti, Vannucchi, Guglielmelli, Mazzarini, Barosi, Genova and Migliaccio.

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Auteurs

Maria Zingariello (M)

Unit of Microscopic and Ultrastructural Anatomy, Department of Medicine, University Campus Bio-Medico, Rome, Italy.

Vittorio Rosti (V)

Center for the Study of Myelofibrosis, Laboratory of Biochemistry Biotechnology and Advanced Diagnosis, IRCCS Policlinico San Matteo, Pavia, Italy.

Alessandro M Vannucchi (AM)

CRIMM; Center Research and Innovation of Myeloproliferative Neoplasms, AOUC, University of Florence, Florence, Italy.

Paola Guglielmelli (P)

CRIMM; Center Research and Innovation of Myeloproliferative Neoplasms, AOUC, University of Florence, Florence, Italy.

Maria Mazzarini (M)

Biomedical and Neuromotor Sciences, Alma Mater University Bologna, Bologna, Italy.

Giovanni Barosi (G)

Center for the Study of Myelofibrosis, Laboratory of Biochemistry Biotechnology and Advanced Diagnosis, IRCCS Policlinico San Matteo, Pavia, Italy.

Maria Luisa Genova (ML)

Biomedical and Neuromotor Sciences, Alma Mater University Bologna, Bologna, Italy.

Anna Rita Migliaccio (AR)

Biomedical and Neuromotor Sciences, Alma Mater University Bologna, Bologna, Italy.
Myeloproliferative Neoplasm-Research Consortium, New York, NY, United States.

Classifications MeSH