Colombia | info:eu-repo/semantics/article
dc.creatorUrcuqui Inchima, Silvio
dc.creatorVelilla Hernández, Paula Andrea
dc.creatorTamayo Molina, Yordi Sebastián
dc.creatorHernández Sarmiento, Lady Johana
dc.date2023-06-15T18:10:26Z
dc.date2023-06-15T18:10:26Z
dc.date2023
dc.date.accessioned2024-04-23T17:44:22Z
dc.date.available2024-04-23T17:44:22Z
dc.identifierTamayo-Molina YS, Velilla PA, Hernández-Sarmiento LJ, Urcuqui-Inchima S. Multitranscript analysis reveals an effect of 2-deoxy-d-glucose on gene expression linked to unfolded protein response and integrated stress response in primary human monocytes and monocyte-derived macrophages. Biochim Biophys Acta Gen Subj. 2023 Jun 7;1867(9):130397. doi: 10.1016/j.bbagen.2023.130397. Epub ahead of print. PMID: 37290716.
dc.identifier0304-4165
dc.identifierhttps://hdl.handle.net/10495/35522
dc.identifier10.1016/j.bbagen.2023.130397
dc.identifier1872-8006
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/9229825
dc.descriptionABSTRACT: Background: Glycolytic inhibitor 2-deoxy-D-glucose (2-DG) binds to hexokinase in a non-competitive manner and phosphoglucose isomerase in a competitive manner, blocking the initial steps of the glycolytic pathway. Although 2-DG stimulates endoplasmic reticulum (ER) stress, activating the unfolded protein response to restore protein homeostasis, it is unclear which ER stress-related genes are modulated in response to 2-DG treatment in human primary cells. Here, we aimed to determine whether the treatment of monocytes and monocyte-derived macrophages (MDMs) with 2-DG leads to a transcriptional profile specific to ER stress. Methods: We performed bioinformatics analysis to identify differentially expressed genes (DEGs) in previously reported RNA-seq datasets of 2-DG treated cells. RT-qPCR was performed to verify the sequencing data on cultured MDMs. Results: A total of 95 common DEGs were found by transcriptional analysis of monocytes and MDMs treated with 2-DG. Among these, 74 were up-regulated and 21 were down-regulated. Multitranscript analysis showed that DEGs are linked to integrated stress response (GRP78/BiP, PERK, ATF4, CHOP, GADD34, IRE1α, XBP1, SESN2, ASNS, PHGDH), hexosamine biosynthetic pathway (GFAT1, GNA1, PGM3, UAP1), and mannose metabolism (GMPPA and GMPPB). Conclusions: Results reveal that 2-DG triggers a gene expression program that might be involved in restoring protein homeostasis in primary cells. General significance: 2-DG is known to inhibit glycolysis and induce ER stress; however, its effect on gene expression in primary cells is not well understood. This work shows that 2-DG is a stress inducer shifting the metabolic state of monocytes and macrophages
dc.descriptionCOL0012444
dc.format9
dc.formatapplication/pdf
dc.formatapplication/pdf
dc.formatapplication/vnd.openxmlformats-officedocument.wordprocessingml.document
dc.languageeng
dc.publisherElsevier
dc.publisherInmunovirología
dc.publisherÁmsterdam, Países Bajos
dc.relationBiochim. Biophys. Acta, Gen. Subj.
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/2.5/co/
dc.rightshttp://purl.org/coar/access_right/c_abf2
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectDesoxiglucosa
dc.subjectDeoxyglucose
dc.subjectEstrés del Retículo Endoplásmico
dc.subjectEndoplasmic Reticulum Stress
dc.subjectRespuesta de Proteína Desplegada
dc.subjectUnfolded Protein Response
dc.subjectGlicosilación
dc.subjectGlycosylation
dc.subjectCélulas
dc.subjectCells
dc.titleMultitranscript analysis reveals an effect of 2-deoxy-d-glucose on gene expression linked to unfolded protein response and integrated stress response in primary human monocytes and monocyte-derived macrophages
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typehttp://purl.org/coar/resource_type/c_2df8fbb1
dc.typehttps://purl.org/redcol/resource_type/ART
dc.typeArtículo de investigación


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