NRF2 Deficiency in Bladder Epithelial Cells Owing to Ubiquitination by N6-Methyladenosine-Modified TRIM21 Induces Oxidative Stress and Inflammation to Aggravate IC/BPS
Zongyao Fan,1,* Qingyu Ge,2,* Bin Ni,1,* Junjie Zhang,1 Tianpeng Du,1 Hewei Xu,3 Zheng Duan,1 Sicong Zhang,1 Chao Wang,4 Jun Xue,1 Feng Ling,5 Zhengsen Chen,1 Baixin Shen,1 Zhongqing Wei1 1Department of Urology, The Second Affiliated Hospital of Nanjing Medical Un...
Saved in:
| Main Authors: | , , , , , , , , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Dove Medical Press
2025-08-01
|
| Series: | Journal of Inflammation Research |
| Subjects: | |
| Online Access: | https://www.dovepress.com/nrf2-deficiency-in-bladder-epithelial-cells-owing-to-ubiquitination-by-peer-reviewed-fulltext-article-JIR |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| _version_ | 1849225519907733504 |
|---|---|
| author | Fan Z Ge Q Ni B Zhang J Du T Xu H Duan Z Zhang S Wang C Xue J Ling F Chen Z Shen B Wei Z |
| author_facet | Fan Z Ge Q Ni B Zhang J Du T Xu H Duan Z Zhang S Wang C Xue J Ling F Chen Z Shen B Wei Z |
| author_sort | Fan Z |
| collection | DOAJ |
| description | Zongyao Fan,1,* Qingyu Ge,2,* Bin Ni,1,* Junjie Zhang,1 Tianpeng Du,1 Hewei Xu,3 Zheng Duan,1 Sicong Zhang,1 Chao Wang,4 Jun Xue,1 Feng Ling,5 Zhengsen Chen,1 Baixin Shen,1 Zhongqing Wei1 1Department of Urology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, 210000, People’s Republic of China; 2Department of Urology, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, 200000, People’s Republic of China; 3Department of Urology, Children’s Hospital of Nanjing Medical University, Nanjing, 210000, People’s Republic of China; 4Department of Urology, Songjiang Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200000, People’s Republic of China; 5Department of Urology, Ningguo City People’s Hospital, Ningguo, 242300, People’s Republic of China*These authors contributed equally to this workCorrespondence: Zhongqing Wei, Email weizq@njmu.edu.cn Baixin Shen, Email baixinshen@njmu.edu.cnBackground: Interstitial cystitis/bladder pain syndrome (IC/BPS) has become a pressing clinical issue due to its unclear etiology and severe, persistent pelvic pain. Despite extensive research, the pathogenesis of IC/BPS remains unresolved, and current treatments primarily target symptom relief rather than addressing underlying disease mechanisms. This study aimed to investigate the effects of nuclear factor erythroid 2-related factor 2 (NRF2) on IC/BPS and the potential molecular mechanisms.Methods: Bladder mucosal biopsies from IC/BPS patients were subjected to RT-qPCR and immunoblotting to quantify NRF2 mRNA/protein expression. In vivo modeling, WT and NRF2 gene knockout mice received intraperitoneal cyclophosphamide to induce cystitis. Bladder function was assessed via Void Spot Assays, and Urodynamic. In vitro validation, LPS-stimulated SV-HUC-1 cells were transduced with NRF2 knockdown or overexpression, and oxidative stress and inflammation levels were evaluated. Then, the molecular mechanism of NRF2 in IC/BPS was determined by conducting Western blot, mass spectrometry, co-immunoprecipitation, and RT-qPCR analyses.Results: This study identified markedly reduced expression of NRF2 in the lesional bladder mucosa of patients with IC/BPS. By employing NRF2 knockout mice and cellular models of bladder inflammation, the essential role of NRF2 in modulating oxidative stress and inflammation was underscored. Furthermore, tripartite motif-containing 21 (TRIM21) interacted with NRF2, promoting its degradation via ubiquitination in bladder epithelial cell lines, thus elucidating TRIM21’s regulatory role in bladder inflammation. Additionally, N6-methyladenosine (M6A) modifications recognized by IGF2BP2 enhanced TRIM21 expression by stabilizing TRIM21 mRNA.Conclusion: This study positions the TRIM21-NRF2 axis as a key regulator of oxidative stress and inflammation in IC/BPS and suggests it as a promising therapeutic target for future IC/BPS interventions.Keywords: IC/BPS, NRF2, TRIM21, ubiquitination, N6-methyladenosine |
| format | Article |
| id | doaj-art-f9c787e01f4e48d08d4ae2685ca2fd84 |
| institution | Kabale University |
| issn | 1178-7031 |
| language | English |
| publishDate | 2025-08-01 |
| publisher | Dove Medical Press |
| record_format | Article |
| series | Journal of Inflammation Research |
| spelling | doaj-art-f9c787e01f4e48d08d4ae2685ca2fd842025-08-24T17:31:58ZengDove Medical PressJournal of Inflammation Research1178-70312025-08-01Volume 18Issue 11157711592106119NRF2 Deficiency in Bladder Epithelial Cells Owing to Ubiquitination by N6-Methyladenosine-Modified TRIM21 Induces Oxidative Stress and Inflammation to Aggravate IC/BPSFan Z0Ge Q1Ni B2Zhang JDu TXu HDuan ZZhang S3Wang C4Xue J5Ling F6Chen Z7Shen B8Wei Z9UrologyUrologyUrologyUrologyUrologyUrologyUrologyUrologyurologyThe Second Affiliated Hospital of Nanjing Medical UniversityZongyao Fan,1,* Qingyu Ge,2,* Bin Ni,1,* Junjie Zhang,1 Tianpeng Du,1 Hewei Xu,3 Zheng Duan,1 Sicong Zhang,1 Chao Wang,4 Jun Xue,1 Feng Ling,5 Zhengsen Chen,1 Baixin Shen,1 Zhongqing Wei1 1Department of Urology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, 210000, People’s Republic of China; 2Department of Urology, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, 200000, People’s Republic of China; 3Department of Urology, Children’s Hospital of Nanjing Medical University, Nanjing, 210000, People’s Republic of China; 4Department of Urology, Songjiang Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200000, People’s Republic of China; 5Department of Urology, Ningguo City People’s Hospital, Ningguo, 242300, People’s Republic of China*These authors contributed equally to this workCorrespondence: Zhongqing Wei, Email weizq@njmu.edu.cn Baixin Shen, Email baixinshen@njmu.edu.cnBackground: Interstitial cystitis/bladder pain syndrome (IC/BPS) has become a pressing clinical issue due to its unclear etiology and severe, persistent pelvic pain. Despite extensive research, the pathogenesis of IC/BPS remains unresolved, and current treatments primarily target symptom relief rather than addressing underlying disease mechanisms. This study aimed to investigate the effects of nuclear factor erythroid 2-related factor 2 (NRF2) on IC/BPS and the potential molecular mechanisms.Methods: Bladder mucosal biopsies from IC/BPS patients were subjected to RT-qPCR and immunoblotting to quantify NRF2 mRNA/protein expression. In vivo modeling, WT and NRF2 gene knockout mice received intraperitoneal cyclophosphamide to induce cystitis. Bladder function was assessed via Void Spot Assays, and Urodynamic. In vitro validation, LPS-stimulated SV-HUC-1 cells were transduced with NRF2 knockdown or overexpression, and oxidative stress and inflammation levels were evaluated. Then, the molecular mechanism of NRF2 in IC/BPS was determined by conducting Western blot, mass spectrometry, co-immunoprecipitation, and RT-qPCR analyses.Results: This study identified markedly reduced expression of NRF2 in the lesional bladder mucosa of patients with IC/BPS. By employing NRF2 knockout mice and cellular models of bladder inflammation, the essential role of NRF2 in modulating oxidative stress and inflammation was underscored. Furthermore, tripartite motif-containing 21 (TRIM21) interacted with NRF2, promoting its degradation via ubiquitination in bladder epithelial cell lines, thus elucidating TRIM21’s regulatory role in bladder inflammation. Additionally, N6-methyladenosine (M6A) modifications recognized by IGF2BP2 enhanced TRIM21 expression by stabilizing TRIM21 mRNA.Conclusion: This study positions the TRIM21-NRF2 axis as a key regulator of oxidative stress and inflammation in IC/BPS and suggests it as a promising therapeutic target for future IC/BPS interventions.Keywords: IC/BPS, NRF2, TRIM21, ubiquitination, N6-methyladenosinehttps://www.dovepress.com/nrf2-deficiency-in-bladder-epithelial-cells-owing-to-ubiquitination-by-peer-reviewed-fulltext-article-JIRIC/BPSNRF2TRIM21UbiquitinationN6-methyladenosine. |
| spellingShingle | Fan Z Ge Q Ni B Zhang J Du T Xu H Duan Z Zhang S Wang C Xue J Ling F Chen Z Shen B Wei Z NRF2 Deficiency in Bladder Epithelial Cells Owing to Ubiquitination by N6-Methyladenosine-Modified TRIM21 Induces Oxidative Stress and Inflammation to Aggravate IC/BPS Journal of Inflammation Research IC/BPS NRF2 TRIM21 Ubiquitination N6-methyladenosine. |
| title | NRF2 Deficiency in Bladder Epithelial Cells Owing to Ubiquitination by N6-Methyladenosine-Modified TRIM21 Induces Oxidative Stress and Inflammation to Aggravate IC/BPS |
| title_full | NRF2 Deficiency in Bladder Epithelial Cells Owing to Ubiquitination by N6-Methyladenosine-Modified TRIM21 Induces Oxidative Stress and Inflammation to Aggravate IC/BPS |
| title_fullStr | NRF2 Deficiency in Bladder Epithelial Cells Owing to Ubiquitination by N6-Methyladenosine-Modified TRIM21 Induces Oxidative Stress and Inflammation to Aggravate IC/BPS |
| title_full_unstemmed | NRF2 Deficiency in Bladder Epithelial Cells Owing to Ubiquitination by N6-Methyladenosine-Modified TRIM21 Induces Oxidative Stress and Inflammation to Aggravate IC/BPS |
| title_short | NRF2 Deficiency in Bladder Epithelial Cells Owing to Ubiquitination by N6-Methyladenosine-Modified TRIM21 Induces Oxidative Stress and Inflammation to Aggravate IC/BPS |
| title_sort | nrf2 deficiency in bladder epithelial cells owing to ubiquitination by n6 methyladenosine modified trim21 induces oxidative stress and inflammation to aggravate ic bps |
| topic | IC/BPS NRF2 TRIM21 Ubiquitination N6-methyladenosine. |
| url | https://www.dovepress.com/nrf2-deficiency-in-bladder-epithelial-cells-owing-to-ubiquitination-by-peer-reviewed-fulltext-article-JIR |
| work_keys_str_mv | AT fanz nrf2deficiencyinbladderepithelialcellsowingtoubiquitinationbyn6methyladenosinemodifiedtrim21inducesoxidativestressandinflammationtoaggravateicbps AT geq nrf2deficiencyinbladderepithelialcellsowingtoubiquitinationbyn6methyladenosinemodifiedtrim21inducesoxidativestressandinflammationtoaggravateicbps AT nib nrf2deficiencyinbladderepithelialcellsowingtoubiquitinationbyn6methyladenosinemodifiedtrim21inducesoxidativestressandinflammationtoaggravateicbps AT zhangj nrf2deficiencyinbladderepithelialcellsowingtoubiquitinationbyn6methyladenosinemodifiedtrim21inducesoxidativestressandinflammationtoaggravateicbps AT dut nrf2deficiencyinbladderepithelialcellsowingtoubiquitinationbyn6methyladenosinemodifiedtrim21inducesoxidativestressandinflammationtoaggravateicbps AT xuh nrf2deficiencyinbladderepithelialcellsowingtoubiquitinationbyn6methyladenosinemodifiedtrim21inducesoxidativestressandinflammationtoaggravateicbps AT duanz nrf2deficiencyinbladderepithelialcellsowingtoubiquitinationbyn6methyladenosinemodifiedtrim21inducesoxidativestressandinflammationtoaggravateicbps AT zhangs nrf2deficiencyinbladderepithelialcellsowingtoubiquitinationbyn6methyladenosinemodifiedtrim21inducesoxidativestressandinflammationtoaggravateicbps AT wangc nrf2deficiencyinbladderepithelialcellsowingtoubiquitinationbyn6methyladenosinemodifiedtrim21inducesoxidativestressandinflammationtoaggravateicbps AT xuej nrf2deficiencyinbladderepithelialcellsowingtoubiquitinationbyn6methyladenosinemodifiedtrim21inducesoxidativestressandinflammationtoaggravateicbps AT lingf nrf2deficiencyinbladderepithelialcellsowingtoubiquitinationbyn6methyladenosinemodifiedtrim21inducesoxidativestressandinflammationtoaggravateicbps AT chenz nrf2deficiencyinbladderepithelialcellsowingtoubiquitinationbyn6methyladenosinemodifiedtrim21inducesoxidativestressandinflammationtoaggravateicbps AT shenb nrf2deficiencyinbladderepithelialcellsowingtoubiquitinationbyn6methyladenosinemodifiedtrim21inducesoxidativestressandinflammationtoaggravateicbps AT weiz nrf2deficiencyinbladderepithelialcellsowingtoubiquitinationbyn6methyladenosinemodifiedtrim21inducesoxidativestressandinflammationtoaggravateicbps |