Sphingolipid-mediated inflammatory signaling leading to autophagy inhibition converts erythropoiesis to myelopoiesis in human hematopoietic stem/progenitor cells.


Journal

Cell death and differentiation
ISSN: 1476-5403
Titre abrégé: Cell Death Differ
Pays: England
ID NLM: 9437445

Informations de publication

Date de publication:
09 2019
Historique:
received: 15 08 2017
accepted: 19 11 2018
revised: 04 11 2018
pubmed: 14 12 2018
medline: 1 9 2020
entrez: 15 12 2018
Statut: ppublish

Résumé

Elevated levels of the pro-inflammatory cytokine tumor necrosis factor-α (TNFα) inhibit erythropoiesis and cause anemia in patients with cancer and chronic inflammatory diseases. TNFα is also a potent activator of the sphingomyelinase (SMase)/ceramide pathway leading to ceramide synthesis and regulating cell differentiation, proliferation, apoptosis, senescence, and autophagy. Here we evaluated the implication of the TNFα/SMase/ceramide pathway on inhibition of erythropoiesis in human CD34

Identifiants

pubmed: 30546074
doi: 10.1038/s41418-018-0245-x
pii: 10.1038/s41418-018-0245-x
pmc: PMC6748125
doi:

Substances chimiques

Autophagy-Related Protein 5 0
Ceramides 0
Sphingolipids 0
Tumor Necrosis Factor-alpha 0
MTOR protein, human EC 2.7.1.1
Autophagy-Related Protein-1 Homolog EC 2.7.11.1
TOR Serine-Threonine Kinases EC 2.7.11.1
Sphingomyelin Phosphodiesterase EC 3.1.4.12

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1796-1812

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Auteurs

Marion Orsini (M)

Laboratoire de Biologie Moléculaire et Cellulaire du Cancer, Hôpital Kirchberg, 9, rue Edward Steichen, 2540, Luxembourg, Luxembourg.

Sébastien Chateauvieux (S)

Laboratoire de Biologie Moléculaire et Cellulaire du Cancer, Hôpital Kirchberg, 9, rue Edward Steichen, 2540, Luxembourg, Luxembourg.

Jiyun Rhim (J)

Department of Pharmacy, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul, 08826, South Korea.

Anthoula Gaigneaux (A)

Laboratoire de Biologie Moléculaire et Cellulaire du Cancer, Hôpital Kirchberg, 9, rue Edward Steichen, 2540, Luxembourg, Luxembourg.

David Cheillan (D)

Service de Biochimie et Biologie Moléculaire Grand Est, Unité Médicale Pathologies Métaboliques Erythrocytaires et Dépistage Périnatal, Centre de Biologie et de Pathologie Est, Hospices Civils de Lyon, Bron, France.

Christo Christov (C)

Service Commun de Microscopie, Université de Lorraine, Nancy, France.

Mario Dicato (M)

Laboratoire de Biologie Moléculaire et Cellulaire du Cancer, Hôpital Kirchberg, 9, rue Edward Steichen, 2540, Luxembourg, Luxembourg.

Franck Morceau (F)

Laboratoire de Biologie Moléculaire et Cellulaire du Cancer, Hôpital Kirchberg, 9, rue Edward Steichen, 2540, Luxembourg, Luxembourg.

Marc Diederich (M)

Department of Pharmacy, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul, 08826, South Korea. marcdiederich@snu.ac.kr.

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Classifications MeSH