Teresa Pinto, Ana, Laranjeiro Pinto, Marta, Patrícia Cardoso, Ana, Monteiro, Cátia, Teixeira Pinto, Marta, Filipe Maia, André, Castro, Patrícia, Figueira, Rita, Monteiro, Armanda, Marques, Margarida et al (show 6 more authors)
(2022)
Author Correction: Ionizing radiation modulates human macrophages towards a pro-inflammatory phenotype preserving their pro-invasive and pro-angiogenic capacities.
Scientific reports, 12 (1).
4774-.
ISSN 2045-2322, 2045-2322
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PDF
Author Correction Ionizing radiation modulates human macrophages towards a pro-inflammatory phenotype preserving their pro-i.pdf - Other Download (685kB) | Preview |
Abstract
This Article contains an error in the description of the data presented in Figure 2. Each blot demonstrating a protein of interest, or of its phosphorylated form, is matched with the expression of β-actin, used as loading control. The majority of the proteins were separated in different gels, apart from proteins p105, p50 and Bcl-xL which were run in the same gel and have the same loading control. As a result, the Figure 2 legend, “Ionizing radiation induces macrophage NF-κB activation and increases Bcl-xL expression. (A) Evaluation of RelA phosphorylation (Ser536) and RelB, cRel, p100/p52 and p105/p50 subunit expression, 1 and 6 h after irradiation (2, 6 and 10 Gy). (B) RelB nuclear translocation 6 h after macrophage irradiation (10 Gy). Histone deacetylase 1 (HDAC1) and β-actin were used as loading controls for nuclear and cytoplasmic fractions, respectively. (C) Evaluation of Bcl2 and Bcl-xL expression after macrophage irradiation. Western blot images are representative of protein expression/phosphorylation status in distinct donors (at least n = 4), evaluated in two independent experiments.” should read: “Ionizing radiation induces macrophage NF-κB activation and increases Bcl-xL expression. (A) Evaluation of RelA phosphorylation (Ser536) and RelB, cRel, p100/p52 and p105/p50 subunit expression, 1 and 6 h after irradiation (2, 6 and 10 Gy). (B) RelB nuclear translocation 6 h after macrophage irradiation (10 Gy). Histone deacetylase 1 (HDAC1) and β-actin were used as loading controls for nuclear and cytoplasmic fractions, respectively. (C) Evaluation of Bcl2 and Bcl-xL expression after macrophage irradiation. Western blot images are representative of protein expression/phosphorylation status in distinct donors (at least n = 4), evaluated in two independent experiments. The β-actin loading control of the panels comprised by p105, p50 (2A) and Bcl-xL (2C) is the same, since proteins were separated in the same gel electrophoresis.”
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | 3107 Microbiology, 31 Biological Sciences, 32 Biomedical and Clinical Sciences |
| Divisions: | Faculty of Health and Life Sciences Faculty of Health and Life Sciences > Institute of Systems, Molecular and Integrative Biology |
| Depositing User: | Symplectic Admin |
| Date Deposited: | 29 Sep 2023 09:38 |
| Last Modified: | 06 Dec 2024 18:41 |
| DOI: | 10.1038/s41598-022-08498-1 |
| Related URLs: | |
| URI: | https://livrepository.liverpool.ac.uk/id/eprint/3173209 |
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