New insights into organ-specific oxidative stress mechanisms using a novel biosensor zebrafish

被引:26
|
作者
Mourabit, Sulayman [1 ]
Fitzgerald, Jennifer A. [1 ]
Ellis, Robert P. [1 ]
Takesono, Aya [1 ]
Porteus, Cosima S. [1 ]
Trznadel, Maciej [1 ]
Metz, Jeremy [1 ]
Winter, Matthew J. [1 ]
Kudoh, Tetsuhiro [1 ]
Tyler, Charles R. [1 ]
机构
[1] Univ Exeter, Coll Life & Environm Sci, Biosci, Geoffrey Pope Bldg, Exeter EX4 4QD, Devon, England
基金
英国生物技术与生命科学研究理事会;
关键词
Oxidative stress; Zebrafish; Toxicants; Biosensor; FREE-RADICALS; HUMAN-DISEASE; MITOCHONDRIAL DYSFUNCTION; ACETAMINOPHEN; SYSTEM; NRF2; CELLS; NEPHROTOXICITY; ACTIVATION; TOXICITY;
D O I
10.1016/j.envint.2019.105138
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Background: Reactive oxygen species (ROS) arise as a result from, and are essential in, numerous cellular processes. ROS, however, are highly reactive and if left unneutralised by endogenous antioxidant systems, can result in extensive cellular damage and/or pathogenesis. In addition, exposure to a wide range of environmental stressors can also result in surplus ROS production leading to oxidative stress (OS) and downstream tissue toxicity. Objectives: Our aim was to produce a stable transgenic zebrafish line, unrestricted by tissue-specific gene regulation, which was capable of providing a whole organismal, real-time read-out of tissue-specific OS following exposure to a wide range of OS-inducing environmental contaminants and conditions. This model could, therefore, serve as a sensitive and specific mechanistic in vivo biomarker for all environmental conditions that result in OS. Methods: To achieve this aim, we exploited the pivotal role of the electrophile response element (EpRE) as a globally-acting master regulator of the cellular response to OS. To test tissue specificity and quantitative capacity, we selected a range of chemical contaminants known to induce OS in specific organs or tissues, and assessed dose-responsiveness in each using microscopic measures of mCherry fluorescence intensity. Results: We produced the first stable transgenic zebrafish line Tg (3EpRE:hsp70:mCherry) with high sensitivity for the detection of cellular RedOx imbalances, in vivo in near-real time. We applied this new model to quantify OS after exposure to a range of environmental conditions with high resolution and provided quantification both of compound- and tissue-specific ROS-induced toxicity. Discussion: Our model has an extremely diverse range of potential applications not only for biomonitoring of toxicants in aqueous environments, but also in biomedicine for identifying ROS-mediated mechanisms involved in the progression of a number of important human diseases, including cancer.
引用
收藏
页数:9
相关论文
共 50 条
  • [21] Identifying cellular mechanisms of organ-specific metastasis of Ewing sarcoma
    Knizia, H.
    Unland, R.
    Hotfilder, M.
    Korsching, E.
    Dirksen, U.
    Juergens, H.
    Vormoor, J.
    KLINISCHE PADIATRIE, 2008, 220 (03): : 203 - 203
  • [22] Organ-specific mechanisms linking innate and adaptive antifungal immunity
    Drummond, Rebecca A.
    Lionakis, Michail S.
    SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2019, 89 : 78 - 90
  • [23] Immunologic basis for a novel organ-specific therapy: Immunocloaking
    Brasile, Lauren
    Stubenitsky, Bart
    Henry, Nicholas
    Kizjakina, Karina
    TRANSPLANTATION, 2016, 100 (07) : S86 - S87
  • [24] Identifying cellular mechanisms of organ-specific metastasis of Ewing tumours
    Knizia, H.
    Hotfilder, M.
    Vormoor, J.
    KLINISCHE PADIATRIE, 2007, 219 (03): : 186 - 186
  • [25] MOLECULAR MECHANISMS FOR ORGAN-SPECIFIC COLON-CARCINOMA METASTASIS
    RADINSKY, R
    EUROPEAN JOURNAL OF CANCER, 1995, 31A (7-8) : 1091 - 1095
  • [26] Enhanced lipoperoxidation products in pure pancreatic juice: evidence for organ-specific oxidative stress in chronic pancreatitis
    Santini, SA
    Spada, C
    Bononi, F
    Foschia, F
    Mutignani, M
    Perri, V
    Giardina, B
    Silveri, NG
    Costamagna, G
    DIGESTIVE AND LIVER DISEASE, 2003, 35 (12) : 888 - 892
  • [27] Systems glycomics of adult zebrafish identifies organ-specific sialylation and glycosylation patterns
    Nao Yamakawa
    Jorick Vanbeselaere
    Lan-Yi Chang
    Shin-Yi Yu
    Lucie Ducrocq
    Anne Harduin-Lepers
    Junichi Kurata
    Kiyoko F. Aoki-Kinoshita
    Chihiro Sato
    Kay-Hooi Khoo
    Ken Kitajima
    Yann Guerardel
    Nature Communications, 9
  • [28] Systems glycomics of adult zebrafish identifies organ-specific sialylation and glycosylation patterns
    Yamakawa, Nao
    Vanbeselaere, Jorick
    Chang, Lan-Yi
    Yu, Shin-Yi
    Ducrocq, Lucie
    Harduin-Lepers, Anne
    Kurata, Junichi
    Aoki-Kinoshita, Kiyoko F.
    Sato, Chihiro
    Khoo, Kay-Hooi
    Kitajima, Ken
    Guerardel, Yann
    NATURE COMMUNICATIONS, 2018, 9
  • [29] Organ-specific oxidative DNA damage associated with normal birth in rats
    Randerath, E
    Zhou, GD
    Randerath, K
    CARCINOGENESIS, 1996, 17 (12) : 2563 - 2570
  • [30] AN EVALUATION OF MECHANISMS BY WHICH TOLERANCE TO ORGAN-SPECIFIC ANTIGENS IS LOST USING A TRANSGENIC MOUSE MODEL
    MARTIN, L
    MORAWORMS, M
    LUCAS, C
    REYNOLDS, C
    STEWART, TA
    JOURNAL OF IMMUNOLOGY, 1993, 150 (04): : 1234 - 1243