{"title":"高尿酸血症中程序性细胞死亡的调控机制及其疾病相关性","authors":"Heng Sai, Haojun Shen, Jing Fu, Wenhui Liu","doi":"10.3389/fcell.2026.1934197","DOIUrl":null,"url":null,"abstract":"<p><p>Hyperuricaemia (HUA) is a metabolic disorder that can not only predispose patients to gout but also be associated with renal, cardiovascular, and metabolic diseases. Recent evidence has designated programmed cell death (PCD) as a central event that drives tissue injury and inflammation in HUA. Raised soluble urate and exposure to monosodium urate (MSU) crystals activate separate but shared stress and injury pathways, including apoptosis, pyroptosis, ferroptosis, and necroptosis in concert with dysregulated autophagy. These processes converge through oxidative stress, mitochondrial dysfunction and signalling along the inflammasome-immune axis to influence disease progression. Among these cell death modalities, the NOD-like receptor family pyrin domain containing 3 (NLRP3) inflammasome-mediated pyroptosis is a crucial amplifier of urate-induced inflammation and concomitant cellular injury; ferroptosis also contributes to irreversible organ damage along with impaired autophagy. More importantly, extensive crosstalk among these pathways collectively shapes disease trajectory and outcomes. This Review summarises the main regulatory mechanisms that promote PCD during HUA, with a focus on renal injury, cardiovascular damage and metabolic dysregulation. Distinct from pathway-specific summaries, this Review integrates apoptosis, pyroptosis, ferroptosis and necroptosis together with autophagy-related dysfunction into a unified disease-relevance framework linking urate-associated stress, pathway crosstalk and organ-specific injury in HUA. Current limitations and novel therapeutic targets are also discussed to inform basic mechanistic studies together with potential clinical strategies.</p>","PeriodicalId":12448,"journal":{"name":"Frontiers in Cell and Developmental Biology","volume":"14 ","pages":"1934197"},"PeriodicalIF":5.3000,"publicationDate":"2026-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13662232/pdf/","citationCount":"0","resultStr":"{\"title\":\"Regulatory mechanisms of programmed cell death in hyperuricaemia and their disease relevance.\",\"authors\":\"Heng Sai, Haojun Shen, Jing Fu, Wenhui Liu\",\"doi\":\"10.3389/fcell.2026.1934197\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Hyperuricaemia (HUA) is a metabolic disorder that can not only predispose patients to gout but also be associated with renal, cardiovascular, and metabolic diseases. Recent evidence has designated programmed cell death (PCD) as a central event that drives tissue injury and inflammation in HUA. Raised soluble urate and exposure to monosodium urate (MSU) crystals activate separate but shared stress and injury pathways, including apoptosis, pyroptosis, ferroptosis, and necroptosis in concert with dysregulated autophagy. These processes converge through oxidative stress, mitochondrial dysfunction and signalling along the inflammasome-immune axis to influence disease progression. Among these cell death modalities, the NOD-like receptor family pyrin domain containing 3 (NLRP3) inflammasome-mediated pyroptosis is a crucial amplifier of urate-induced inflammation and concomitant cellular injury; ferroptosis also contributes to irreversible organ damage along with impaired autophagy. More importantly, extensive crosstalk among these pathways collectively shapes disease trajectory and outcomes. This Review summarises the main regulatory mechanisms that promote PCD during HUA, with a focus on renal injury, cardiovascular damage and metabolic dysregulation. Distinct from pathway-specific summaries, this Review integrates apoptosis, pyroptosis, ferroptosis and necroptosis together with autophagy-related dysfunction into a unified disease-relevance framework linking urate-associated stress, pathway crosstalk and organ-specific injury in HUA. Current limitations and novel therapeutic targets are also discussed to inform basic mechanistic studies together with potential clinical strategies.</p>\",\"PeriodicalId\":12448,\"journal\":{\"name\":\"Frontiers in Cell and Developmental Biology\",\"volume\":\"14 \",\"pages\":\"1934197\"},\"PeriodicalIF\":5.3000,\"publicationDate\":\"2026-09-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13662232/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in Cell and Developmental Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.3389/fcell.2026.1934197\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2026/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Cell and Developmental Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3389/fcell.2026.1934197","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
Regulatory mechanisms of programmed cell death in hyperuricaemia and their disease relevance.
Hyperuricaemia (HUA) is a metabolic disorder that can not only predispose patients to gout but also be associated with renal, cardiovascular, and metabolic diseases. Recent evidence has designated programmed cell death (PCD) as a central event that drives tissue injury and inflammation in HUA. Raised soluble urate and exposure to monosodium urate (MSU) crystals activate separate but shared stress and injury pathways, including apoptosis, pyroptosis, ferroptosis, and necroptosis in concert with dysregulated autophagy. These processes converge through oxidative stress, mitochondrial dysfunction and signalling along the inflammasome-immune axis to influence disease progression. Among these cell death modalities, the NOD-like receptor family pyrin domain containing 3 (NLRP3) inflammasome-mediated pyroptosis is a crucial amplifier of urate-induced inflammation and concomitant cellular injury; ferroptosis also contributes to irreversible organ damage along with impaired autophagy. More importantly, extensive crosstalk among these pathways collectively shapes disease trajectory and outcomes. This Review summarises the main regulatory mechanisms that promote PCD during HUA, with a focus on renal injury, cardiovascular damage and metabolic dysregulation. Distinct from pathway-specific summaries, this Review integrates apoptosis, pyroptosis, ferroptosis and necroptosis together with autophagy-related dysfunction into a unified disease-relevance framework linking urate-associated stress, pathway crosstalk and organ-specific injury in HUA. Current limitations and novel therapeutic targets are also discussed to inform basic mechanistic studies together with potential clinical strategies.
期刊介绍:
Frontiers in Cell and Developmental Biology is a broad-scope, interdisciplinary open-access journal, focusing on the fundamental processes of life, led by Prof Amanda Fisher and supported by a geographically diverse, high-quality editorial board.
The journal welcomes submissions on a wide spectrum of cell and developmental biology, covering intracellular and extracellular dynamics, with sections focusing on signaling, adhesion, migration, cell death and survival and membrane trafficking. Additionally, the journal offers sections dedicated to the cutting edge of fundamental and translational research in molecular medicine and stem cell biology.
With a collaborative, rigorous and transparent peer-review, the journal produces the highest scientific quality in both fundamental and applied research, and advanced article level metrics measure the real-time impact and influence of each publication.