Evidence map›Paper›PMID 40935835›Full record

ArticleCell death and differentiation2026

NLRP3 autophagic degradation disruption in melanocytes contributes to vitiligo development.

Ke Zeng, Yuqi Zhu, Zhongxin Han, Siyi Xiong, Yan Zhao, Zilong Xiao, Yingchao Xie, Shiyu Jin, Tingru Dong, Lan Lan and 5 more

Abstract read
In one paragraph

Article in Cell death and differentiation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Integrative Transcriptomic and Genetic Analysis PrioritizesClinical, cosmetic and investigational dermatology · 2026
    Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Ke Zeng *Department of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Yuqi Zhu *Department of Dermatology, Hangzhou Third Hospital affiliated to Zhejiang Chinese Medical University, Hangzhou, China.
Zhongxin Han *Department of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Siyi XiongDepartment of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Yan ZhaoDepartment of Dermatology, Traditional Chinese and Western Medicine Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Zilong XiaoDepartment of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Yingchao XieDepartment of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Shiyu JinDepartment of Dermatology, Hangzhou Third Hospital affiliated to Zhejiang Chinese Medical University, Hangzhou, China.
Tingru DongDepartment of Dermatology, Hangzhou Third Hospital affiliated to Zhejiang Chinese Medical University, Hangzhou, China.
Lan LanDepartment of Pharmacy, Hangzhou Third Hospital affiliated to Zhejiang Chinese Medical University, Hangzhou, China.
Weiwei LiuDepartment of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Yongzhong DuInstitute of Pharmaceutics, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China.
Cuiping GuanDepartment of Dermatology, Hangzhou Third People's Hospital, Hangzhou, China. imgcp@zcmu.edu.cn.ORCID 0000-0001-9084-5418
Xiao YuDepartment of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China. xiaoyu523@smu.edu.cn.ORCID 0000-0003-2491-9110
Xiuzu SongDepartment of Dermatology, Hangzhou Third People's Hospital, Hangzhou, China. songxiuzu@zju.edu.cn.ORCID 0000-0002-0747-2516

Funding

Guangzhou Science and Technology Program key projects 2025A04J7166National Natural Science Foundation of China (National Science Foundation of China) 82171741National Natural Science Foundation of China (National Science Foundation of China) 82371761National Natural Science Foundation of China (National Science Foundation of China) 82473549
6 · The paper itself

Abstract

NLRP3 functions as a critical intracellular danger sensor for inflammasome activation, playing a crucial role in autoimmune diseases. Vitiligo progression has been linked to NLRP3, yet its specific involvement in melanocytes of vitiligo remains poorly understood. In this study, we demonstrate that NLRP3 expression is significantly upregulated in the melanocytes of vitiligo patients and melanoma-Treg-induced vitiligo mouse model. Genetic knockout of NLRP3 effectively alleviates vitiligo progression in these mice. Our mechanistic investigations reveal that the downregulation of the E3 ligase β-TrCP1 in vitiligo melanocytes decreases K27-linked ubiquitination levels of NLRP3, which in turn weakens its interaction with the autophagy receptor NDP52. This disruption impairs the selective autophagic degradation of NLRP3, leading to hyperactivation of inflammation and pyroptosis in melanocytes, thereby accelerating vitiligo pathogenesis. Notably, melanocyte-specific knockdown of NLRP3 using lysine-proline-valine (KPV)-modified deformable liposomes (KPV-Lipos) carrying Nlrp3 shRNA significantly alleviates vitiligo development. This study elucidates the mechanism by which autophagy dysfunction mediated excessive NLRP3 inflammasome activation in melanocytes contributes to vitiligo pathogenesis, highlighting potential therapeutic strategies targeting these pathways for the treatment of vitiligo and other pigment-related skin diseases. Overview of disrupted NLRP3 autophagic degradation in vitiligo melanocytes. In healthy melanocytes, NLRP3 expression is upregulated when subjected to oxidative stress, along with an increase in the E3 ligase β-TrCP1, which enhances the K27-linked ubiquitination of NLRP3 and further strengthens its binding to the autophagy receptor protein NDP52, thus effectively suppressing the excessive inflammatory response. Whereas in the melanocytes of vitiligo patients, decreased expression of β-TrCP1 leads to downregulation of K27-linked ubiquitination in NLRP3, thus inhibiting its autophagic degradation. The persistent activation of NLRP3 in vitiligo melanocytes promotes the cleavage of pro-IL-1β and GSDMD. GSDMD-N subsequently forms pores on the cell membrane, which causes the release of IL-1β and results in melanocyte pyroptosis. In our study, we utilize KPV-Lipos with Nlrp3 shRNA to precisely knockdown NLRP3 expression in melanocytes and effectively alleviate vitiligo development, which provide a potentially promising strategy for the treatment of vitiligo. MC, melanocytes.

Indexed as

AutophagyMelanocytesNLR Family, Pyrin Domain-Containing 3 ProteinVitiligoAnimalsbeta-Transducin Repeat-Containing ProteinsDisease Models, AnimalHumansInflammasomesMaleMiceMice, Inbred C57BLMice, KnockoutUbiquitinationbeta-Transducin Repeat-Containing ProteinsInflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, human

Identifiers

PMID40935835
PMCPMC12881556

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.