4.7 Article

Biotransformation of soluble-insoluble lanthanum species and its induced NLRP3 inflammasome activation and chronic fibrosis*

期刊

ENVIRONMENTAL POLLUTION
卷 284, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.envpol.2021.117438

关键词

Lanthanum(III); Insoluble species; Biotransformation; NLRP3 inflammasome; Fibrosis

资金

  1. National Natural Science Foundation of China [21777152, 31971322]
  2. Science and Technology Development Project Foundation of Jilin Province [20200404129YY]
  3. budgetary construction funds of Jilin Province [2020C035-4]
  4. National Basic Research Program of China [2020YFA0710702, 2016YFA0203200]
  5. Users with Excellence Project of the Hefei Science Center CAS [2018HSC-UE004]

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The study found that insoluble La(III) species formed under physiological conditions can activate the NLRP3 inflammasome, leading to chronic toxicity, possibly due to K+ efflux and lysosomal rupture. Mice exposed to soluble La(III) species daily for 90 days showed activation of the NLRP3 inflammasome in liver and kidney, resulting in chronic fibrosis, which may be related to the formation of insoluble La(III) species.
Soluble lanthanum (La)(III) species that have been extensively used as fertilizers in agriculture can potentially get into the human body through foods and environment. Most soluble La(III) species can rapidly transform into insoluble La(III) species under physiological conditions, however, their potential biological behavior and chronic toxicity are rarely investigated. In the present study, insoluble La(III) species formed under physiological condition were identified as nanoscale or microscale particles, and their major components were found to experience biotransformation process upon contact with cells. Insoluble La(III) species could adhere to extracellular membrane or be internalized into cells, capable of activating a nucleotide-binding domain and leucine-rich repeat protein 3 (NLRP3) inflammasome. The underlying mechanism could be ascribed to K+ efflux and lysosomal rupture because these insoluble La(III) species locating at extracellular membrane could reduce the unsaturated fatty acids of cell membrane, leading to potassium (K+) efflux, and those internalized into cells could consume the phospholipids of lysosomal membrane, leading to lysosomal rupture. Mice daily drinking soluble La (III) species to mimic drinking tea process for 90 days were found to present NLRP3 inflammasome activation in liver and kidney, as a result of chronic fibrosis, which is potentially correlated to insoluble La(III) species formation.

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