The organophosphate pesticide methamidophos opens the blood-testis barrier and covalently binds to ZO-2 in mice
Creators
- 1. Department of Physiology, Biophysics and Neuroscience, Cinvestav, Mexico City 07360 (Mexico)
- 2. Max Planck Institute for Chemical Ecology, Jena 07745 (Germany)
- 3. Department of Biotechnology and Biochemistry, Cinvestav, Irapuato 36824 (Mexico)
- 4. Department of Toxicology, Cinvestav, Mexico City 07360 (Mexico)
- 5. Department of Infectomics and Molecular Pathogenesis, Cinvestav, Mexico City 07360 (Mexico)
Description
Highlights: • The organophosphate pesticide methamidophos opens the blood-testis barrier • Methamidophos triggers the appearance of immature germ cells in the epididymis • Methamidophos changes stage-specific expression of blood-testis barrier proteins • Methamidophos induces the phosphorylation of ZO-2 and occludin in testes • Methamidophos forms covalent bonds with ZO-2 Methamidophos (MET) is an organophosphate (OP) pesticide widely used in agriculture in developing countries. MET causes adverse effects in male reproductive function in humans and experimental animals, but the underlying mechanisms remain largely unknown. We explored the effect of MET on mice testes (5 mg/kg/day/4 days), finding that this pesticide opens the blood-testis barrier and perturbs spermatogenesis, generating the appearance of immature germ cells in the epididymis. In the seminiferous tubules, MET treatment changed the level of expression or modified the stage-specific localization of tight junction (TJ) proteins ZO-1, ZO-2, occludin, and claudin-3. In contrast, claudin-11 was barely altered. MET also modified the shape of claudin-11, and ZO-2 at the cell border, from a zigzag to a more linear pattern. In addition, MET diminished the expression of ZO-2 in spermatids present in seminiferous tubules, induced the phosphorylation of ZO-2 and occludin in testes and reduced the interaction between these proteins assessed by co-immunoprecipitation. MET formed covalent bonds with ZO-2 in serine, tyrosine and lysine residues. The covalent modifications formed on ZO-2 at putative phosphorylation sites might interfere with ZO-2 interaction with regulatory molecules and other TJ proteins. MET bonds formed at ZO-2 ubiquitination sites likely interfere with ZO-2 degradation and TJ sealing, based on results obtained in cultured epithelial cells transfected with ZO-2 mutated at a MET target lysine residue. Our results shed light on MET male reproductive toxicity and are important to improve regulations regarding the use of OP pesticides and to protect the health of agricultural workers.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.taap.2018.10.003Additional details
Identifiers
- DOI
- 10.1016/j.taap.2018.10.003;
- PII
- S0041008X18304617;
Publishing Information
- Journal Title
- Toxicology and Applied Pharmacology
- Journal Volume
- 360
- Journal Page Range
- p. 257-272
- ISSN
- 0041-008X
- CODEN
- TXAPA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54106824
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- BLOOD; LYSINE; MICE; SPERMATOGENESIS; SPERMATOZOA; TESTES; TYROSINE
- Descriptors DEC
- AMINO ACIDS; ANIMALS; BIOLOGICAL MATERIALS; BODY; BODY FLUIDS; CARBOXYLIC ACIDS; GAMETES; GAMETOGENESIS; GERM CELLS; GONADS; HYDROXY ACIDS; MALE GENITALS; MAMMALS; MATERIALS; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANS; RODENTS; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2018 Elsevier Inc. All rights reserved.