Reduced Peritoneal NRF2 Immunoreactivity in Encapsulating Peritoneal Sclerosis and Its Implications for Redox Homeostasis.
4 affiliations
- 1Dr. Margarete Fischer-Bosch Institute for Clinical Pharmacology, Auerbachstr. 112, 70376 Stuttgart, Germany.
- 2University of Tübingen, Geschwister-Scholl-Platz, 72074 Tübingen, Germany.
- 3Department of General and Visceral Surgery, Robert Bosch Hospital Stuttgart, Auerbachstr. 110, 70376 Stuttgart, Germany.
- 4Department of Internal Medicine and Nephrology, Robert Bosch Hospital Stuttgart, Auerbachstr. 110, 70376 Stuttgart, Germany.
Abstract
Peritoneal dialysis (PD) is an effective modality of renal replacement therapy that provides patients with a high degree of autonomy. However, its long-term use is limited by the detrimental effects of PD fluids on the structure and function of the peritoneal membrane, ultimately leading to a loss of dialysis efficacy. Disruption of redox homeostasis plays a central role in these pathological changes, highlighting the importance of endogenous defense mechanisms in maintaining membrane integrity. Nuclear factor erythroid 2-related factor 2 (NRF2) is a key transcription factor regulating cellular antioxidant and cytoprotective responses. However, its immunoreactivity and localization in the peritoneal tissue of PD patients and patients with encapsulating peritoneal sclerosis (EPS) have not been well characterized. Therefore, we analyzed peritoneal biopsies from healthy controls, pre-dialysis patients, PD patients, and EPS patients. Immunohistochemical analysis demonstrated significantly reduced NRF2 immunoreactivity in patients with EPS compared with all other study groups. In contrast, nuclear factor kappa-light-chain-enhancer of activated B cells (NFκB) immunoreactivity was increased in PD and EPS patients. These results suggest that dysregulation of the NRF2-NFκB axis may be involved in peritoneal membrane injury, which warrants its further investigation as a potential target for preserving peritoneal membrane integrity during long-term PD.
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BibTeX
@article{oberacker2026reduced,
title = {{Reduced Peritoneal NRF2 Immunoreactivity in Encapsulating Peritoneal Sclerosis and Its Implications for Redox Homeostasis.}},
author = {Tina Oberacker and Öztin Tüfek and Tobias Leibold and Adrian Salega and Rebekka Schier and Meng Dong and Leonie Kraft and Jörg Latus and Severin Schricker and Moritz Schanz},
journal = {Antioxidants (Basel, Switzerland)},
year = {2026},
month = sep,
doi = {10.3390/antiox15101234},
url = {https://europepmc.org/article/MED/42939808},
note = {CC BY},
}
RIS
TY - JOUR
TI - Reduced Peritoneal NRF2 Immunoreactivity in Encapsulating Peritoneal Sclerosis and Its Implications for Redox Homeostasis.
AU - Tina Oberacker
AU - Öztin Tüfek
AU - Tobias Leibold
AU - Adrian Salega
AU - Rebekka Schier
AU - Meng Dong
AU - Leonie Kraft
AU - Jörg Latus
AU - Severin Schricker
AU - Moritz Schanz
PY - 2026
DA - 2026/09/24
JO - Antioxidants (Basel, Switzerland)
DO - 10.3390/antiox15101234
UR - https://europepmc.org/article/MED/42939808
AB - Peritoneal dialysis (PD) is an effective modality of renal replacement therapy that provides patients with a high degree of autonomy. However, its long-term use is limited by the detrimental effects of PD fluids on the structure and function of the peritoneal membrane, ultimately leading to a loss of dialysis efficacy. Disruption of redox homeostasis plays a central role in these pathological changes, highlighting the importance of endogenous defense mechanisms in maintaining membrane integrity. Nuclear factor erythroid 2-related factor 2 (NRF2) is a key transcription factor regulating cellular antioxidant and cytoprotective responses. However, its immunoreactivity and localization in the peritoneal tissue of PD patients and patients with encapsulating peritoneal sclerosis (EPS) have not been well characterized. Therefore, we analyzed peritoneal biopsies from healthy controls, pre-dialysis patients, PD patients, and EPS patients. Immunohistochemical analysis demonstrated significantly reduced NRF2 immunoreactivity in patients with EPS compared with all other study groups. In contrast, nuclear factor kappa-light-chain-enhancer of activated B cells (NFκB) immunoreactivity was increased in PD and EPS patients. These results suggest that dysregulation of the NRF2-NFκB axis may be involved in peritoneal membrane injury, which warrants its further investigation as a potential target for preserving peritoneal membrane integrity during long-term PD.
SN - 2076-3921
ER -