{"title":"多卤代咔唑通过调节秀丽隐杆线虫液-液相分离失调损害多巴胺能神经元。","authors":"Yuhang Luo, Hongbo Xu, Pei Peng, Xinhe Lu, Qian Zhou, Ziqing Gao, Cheng Tang, Hongyan Yin, Ying Cai, Gaga Mahai, Zhiqiang Zhu, Zuojun Liu, Hanzeng Li, Shunqing Xu","doi":"10.1002/advs.202502486","DOIUrl":null,"url":null,"abstract":"<p><p>Polyhalogenated carbazoles (PHCZ) are emerging organic pollutants derived from a variety of natural and synthetic sources. While PHCZ have raised environmental concerns due to its persistence, bioaccumulation, and widespread distribution, its neuronal toxicity remains largely understudied. Here, the general and neuronal toxicity of PHCZ using the model organism Caenorhabditis elegans (C. elegans) is evaluated. It is found that PHCZ can induce significant dopaminergic neurodegeneration, in addition to exhibiting general toxicity affecting development and male gamete differentiation. Mechanistically, PHCZ promote liquid-liquid phase separation (LLPS) of the Parkinson's disease (PD)-associated protein α-synuclein (α-syn), and reduces the fluidity of the resultant condensate both in vitro and in vivo. PHCZ disrupts general protein homeostasis and specifically activates the unfolded protein response in the ER (UPR<sup>ER</sup>) through the IRE-1 signaling axis. Moreover, PHCZ impairs mitochondrial functions, providing another mechanistic link to neuronal degeneration. Thus, this study uncovers a hitherto unrecognized neuronal toxicity of PHCZ, which is partly attributed to their capacity to dysregulate LLPS and UPR<sup>ER</sup>, offering new insights into their potential health risks.</p>","PeriodicalId":117,"journal":{"name":"Advanced Science","volume":" ","pages":"e02486"},"PeriodicalIF":14.1000,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Polyhalogenated Carbazole Impairs Dopaminergic Neurons through Dysregulation of Liquid-Liquid Phase Separation in Caenorhabditis elegans.\",\"authors\":\"Yuhang Luo, Hongbo Xu, Pei Peng, Xinhe Lu, Qian Zhou, Ziqing Gao, Cheng Tang, Hongyan Yin, Ying Cai, Gaga Mahai, Zhiqiang Zhu, Zuojun Liu, Hanzeng Li, Shunqing Xu\",\"doi\":\"10.1002/advs.202502486\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Polyhalogenated carbazoles (PHCZ) are emerging organic pollutants derived from a variety of natural and synthetic sources. While PHCZ have raised environmental concerns due to its persistence, bioaccumulation, and widespread distribution, its neuronal toxicity remains largely understudied. Here, the general and neuronal toxicity of PHCZ using the model organism Caenorhabditis elegans (C. elegans) is evaluated. It is found that PHCZ can induce significant dopaminergic neurodegeneration, in addition to exhibiting general toxicity affecting development and male gamete differentiation. Mechanistically, PHCZ promote liquid-liquid phase separation (LLPS) of the Parkinson's disease (PD)-associated protein α-synuclein (α-syn), and reduces the fluidity of the resultant condensate both in vitro and in vivo. PHCZ disrupts general protein homeostasis and specifically activates the unfolded protein response in the ER (UPR<sup>ER</sup>) through the IRE-1 signaling axis. Moreover, PHCZ impairs mitochondrial functions, providing another mechanistic link to neuronal degeneration. Thus, this study uncovers a hitherto unrecognized neuronal toxicity of PHCZ, which is partly attributed to their capacity to dysregulate LLPS and UPR<sup>ER</sup>, offering new insights into their potential health risks.</p>\",\"PeriodicalId\":117,\"journal\":{\"name\":\"Advanced Science\",\"volume\":\" \",\"pages\":\"e02486\"},\"PeriodicalIF\":14.1000,\"publicationDate\":\"2025-10-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Science\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/advs.202502486\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Science","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/advs.202502486","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Polyhalogenated Carbazole Impairs Dopaminergic Neurons through Dysregulation of Liquid-Liquid Phase Separation in Caenorhabditis elegans.
Polyhalogenated carbazoles (PHCZ) are emerging organic pollutants derived from a variety of natural and synthetic sources. While PHCZ have raised environmental concerns due to its persistence, bioaccumulation, and widespread distribution, its neuronal toxicity remains largely understudied. Here, the general and neuronal toxicity of PHCZ using the model organism Caenorhabditis elegans (C. elegans) is evaluated. It is found that PHCZ can induce significant dopaminergic neurodegeneration, in addition to exhibiting general toxicity affecting development and male gamete differentiation. Mechanistically, PHCZ promote liquid-liquid phase separation (LLPS) of the Parkinson's disease (PD)-associated protein α-synuclein (α-syn), and reduces the fluidity of the resultant condensate both in vitro and in vivo. PHCZ disrupts general protein homeostasis and specifically activates the unfolded protein response in the ER (UPRER) through the IRE-1 signaling axis. Moreover, PHCZ impairs mitochondrial functions, providing another mechanistic link to neuronal degeneration. Thus, this study uncovers a hitherto unrecognized neuronal toxicity of PHCZ, which is partly attributed to their capacity to dysregulate LLPS and UPRER, offering new insights into their potential health risks.
期刊介绍:
Advanced Science is a prestigious open access journal that focuses on interdisciplinary research in materials science, physics, chemistry, medical and life sciences, and engineering. The journal aims to promote cutting-edge research by employing a rigorous and impartial review process. It is committed to presenting research articles with the highest quality production standards, ensuring maximum accessibility of top scientific findings. With its vibrant and innovative publication platform, Advanced Science seeks to revolutionize the dissemination and organization of scientific knowledge.