Wenting Wu, Gaku Ichihara, Akihiko Ikegami, Yuka Suzuki, Kiyora Izuoka, Saleh Ahmed, Cai Zong, Ken Itoh, Masayuki Yamamoto, Sahoko Ichihara
{"title":"Nrf2促进小鼠mwcnt诱导的肺部炎症。","authors":"Wenting Wu, Gaku Ichihara, Akihiko Ikegami, Yuka Suzuki, Kiyora Izuoka, Saleh Ahmed, Cai Zong, Ken Itoh, Masayuki Yamamoto, Sahoko Ichihara","doi":"10.1080/17435390.2025.2529471","DOIUrl":null,"url":null,"abstract":"<p><p>Multi-walled carbon nanotubes (MWCNTs) are used to reinforce plastics, but recent studies have demonstrated that exposure to MWCNTs via inhalation or intratracheal instillation induced lung cancer in rats. The present study was designed to determine the role of nuclear factor erythroid 2-related factor (Nrf2) in MWCNT-induced inflammatory response in the lung of mice. Anesthetized male Nrf2 null mice and age-matched wild-type mice were exposed once to MWCNTs at either 0, 10, or 20 µg/mouse by pharyngeal aspiration. Bronchoalveolar lavage fluid (BALF) and lung tissues were collected after 7 days to evaluate pulmonary inflammation. Exposure to MWCNTs significantly increased BALF total cell counts and total protein level in wild-type mice, but not in Nrf2 null mice. MWCNT-exposed wild-type mice showed the significant increases in interleukin (IL)-1β, IL-6, and keratinocyte-derived chemokines (KC) levels in BALF, but these were not seen in BALF of Nrf2 null mice. Exposure to MWCNTs at 10 and 20 μg/mouse for 7 days did not significantly increase oxidative stress in both genotypes, but exposure to MWCNTs increased the levels of IL-1β and caspase-1 only in the lungs of wild-type mice. Our results demonstrate that Nrf2 promotes MWCNT-induced pulmonary inflammation, probably through inflammasome activation.</p>","PeriodicalId":18899,"journal":{"name":"Nanotoxicology","volume":" ","pages":"1-14"},"PeriodicalIF":3.6000,"publicationDate":"2025-07-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nrf2 promotes MWCNT-induced pulmonary inflammation in mice.\",\"authors\":\"Wenting Wu, Gaku Ichihara, Akihiko Ikegami, Yuka Suzuki, Kiyora Izuoka, Saleh Ahmed, Cai Zong, Ken Itoh, Masayuki Yamamoto, Sahoko Ichihara\",\"doi\":\"10.1080/17435390.2025.2529471\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Multi-walled carbon nanotubes (MWCNTs) are used to reinforce plastics, but recent studies have demonstrated that exposure to MWCNTs via inhalation or intratracheal instillation induced lung cancer in rats. The present study was designed to determine the role of nuclear factor erythroid 2-related factor (Nrf2) in MWCNT-induced inflammatory response in the lung of mice. Anesthetized male Nrf2 null mice and age-matched wild-type mice were exposed once to MWCNTs at either 0, 10, or 20 µg/mouse by pharyngeal aspiration. Bronchoalveolar lavage fluid (BALF) and lung tissues were collected after 7 days to evaluate pulmonary inflammation. Exposure to MWCNTs significantly increased BALF total cell counts and total protein level in wild-type mice, but not in Nrf2 null mice. MWCNT-exposed wild-type mice showed the significant increases in interleukin (IL)-1β, IL-6, and keratinocyte-derived chemokines (KC) levels in BALF, but these were not seen in BALF of Nrf2 null mice. Exposure to MWCNTs at 10 and 20 μg/mouse for 7 days did not significantly increase oxidative stress in both genotypes, but exposure to MWCNTs increased the levels of IL-1β and caspase-1 only in the lungs of wild-type mice. Our results demonstrate that Nrf2 promotes MWCNT-induced pulmonary inflammation, probably through inflammasome activation.</p>\",\"PeriodicalId\":18899,\"journal\":{\"name\":\"Nanotoxicology\",\"volume\":\" \",\"pages\":\"1-14\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-07-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nanotoxicology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/17435390.2025.2529471\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"NANOSCIENCE & NANOTECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanotoxicology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/17435390.2025.2529471","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NANOSCIENCE & NANOTECHNOLOGY","Score":null,"Total":0}
Nrf2 promotes MWCNT-induced pulmonary inflammation in mice.
Multi-walled carbon nanotubes (MWCNTs) are used to reinforce plastics, but recent studies have demonstrated that exposure to MWCNTs via inhalation or intratracheal instillation induced lung cancer in rats. The present study was designed to determine the role of nuclear factor erythroid 2-related factor (Nrf2) in MWCNT-induced inflammatory response in the lung of mice. Anesthetized male Nrf2 null mice and age-matched wild-type mice were exposed once to MWCNTs at either 0, 10, or 20 µg/mouse by pharyngeal aspiration. Bronchoalveolar lavage fluid (BALF) and lung tissues were collected after 7 days to evaluate pulmonary inflammation. Exposure to MWCNTs significantly increased BALF total cell counts and total protein level in wild-type mice, but not in Nrf2 null mice. MWCNT-exposed wild-type mice showed the significant increases in interleukin (IL)-1β, IL-6, and keratinocyte-derived chemokines (KC) levels in BALF, but these were not seen in BALF of Nrf2 null mice. Exposure to MWCNTs at 10 and 20 μg/mouse for 7 days did not significantly increase oxidative stress in both genotypes, but exposure to MWCNTs increased the levels of IL-1β and caspase-1 only in the lungs of wild-type mice. Our results demonstrate that Nrf2 promotes MWCNT-induced pulmonary inflammation, probably through inflammasome activation.
期刊介绍:
Nanotoxicology invites contributions addressing research relating to the potential for human and environmental exposure, hazard and risk associated with the use and development of nano-structured materials. In this context, the term nano-structured materials has a broad definition, including ‘materials with at least one dimension in the nanometer size range’. These nanomaterials range from nanoparticles and nanomedicines, to nano-surfaces of larger materials and composite materials. The range of nanomaterials in use and under development is extremely diverse, so this journal includes a range of materials generated for purposeful delivery into the body (food, medicines, diagnostics and prosthetics), to consumer products (e.g. paints, cosmetics, electronics and clothing), and particles designed for environmental applications (e.g. remediation). It is the nano-size range if these materials which unifies them and defines the scope of Nanotoxicology .
While the term ‘toxicology’ indicates risk, the journal Nanotoxicology also aims to encompass studies that enhance safety during the production, use and disposal of nanomaterials. Well-controlled studies demonstrating a lack of exposure, hazard or risk associated with nanomaterials, or studies aiming to improve biocompatibility are welcomed and encouraged, as such studies will lead to an advancement of nanotechnology. Furthermore, many nanoparticles are developed with the intention to improve human health (e.g. antimicrobial agents), and again, such articles are encouraged. In order to promote quality, Nanotoxicology will prioritise publications that have demonstrated characterisation of the nanomaterials investigated.