Mitochondrial Activity and Unfolded Protein Response are Required for Neutrophil Differentiation

• Published in: Cellular physiology and biochemistry Vol. 47; no. 5; pp. 1936 - 1950
• Main Authors: Tanimura, Ayako, Miyoshi, Keiko, Horiguchi, Taigo, Hagita, Hiroko, Fujisawa, Koichi, Noma, Takafumi
• Format: Journal Article
• Language: English
• Published: Basel, Switzerland S. Karger AG 01.01.2018; Cell Physiol Biochem Press GmbH & Co KG
• Subjects: Activating Transcription Factor 4 - metabolism; Activating Transcription Factor 6 - metabolism; Adipocytes; Apoptosis; ATP; CD11b Antigen - metabolism; Cell culture; Cell Differentiation - physiology; eIF-2 Kinase - metabolism; Endoplasmic reticulum; Energy Metabolism - physiology; ER stress; HL-60; HL-60 Cells; Humans; Kinases; Leukemia; Mitochondria; Mitochondria - metabolism; Mutation; Myelocytic differentiation; Neutropenia; Neutrophils; Neutrophils - cytology; Neutrophils - metabolism; Original Paper; Phosphorylation; Proteins; Signal transduction; Trends; Unfolded protein response; Unfolded Protein Response - physiology; X-Box Binding Protein 1 - metabolism; Japan; ER stress; Mitochondria; HL-60; Myelocytic differentiation; ATP; Unfolded protein response
• ISSN: 1015-8987; 1421-9778; 1421-9778
• DOI: 10.1159/000491464

Background/Aims: Endoplasmic reticulum (ER) stress and unfolded protein response (UPR) are involved in hematopoietic differentiation. However, the mechanistic linkage between ER stress/UPR and hematopoietic differentiation remains unclear. Methods: We used bipotent HL-60 cells as an in vitro hematopoietic differentiation system to investigate the role of ER stress and UPR activity in neutrophil and macrophage differentiation. Results: The in vitro differentiation analysis revealed that ER stress decreased during both neutrophil and macrophage differentiations, and the activities of PERK and ATF6 were decreased and that of IRE1α was increased during neutrophil differentiation in a stage-specific manner. By contrast, the activities of ATF6 and ATF4 decreased during macrophage differentiation. When the cells were treated with oligomycin, the expression of CD11b, a myelocytic differentiation marker, and morphological differentiation were suppressed, and XBP-1 activation was inhibited during neutrophil differentiation, whereas CD11b expression was maintained, and morphological differentiation was not obviously affected during macrophage differentiation. Conclusion: In this study, we demonstrated that neutrophil differentiation is regulated by ER stress/UPR that is supported by mitochondrial ATP supply, in which IRE1α-XBP1 activation is essential. Our findings provide the evidence that mitochondrial energy metabolism may play a critical role in neutrophil differentiation.