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Cytotoxicity by endocrine disruptors through effects on ER Ca2+ transporters, aberrations in Ca2+ signalling pathways and ER stress.
Michelangeli, Francesco; Mohammed, Noor A; Jones, Brogan; Tairu, Monsurat; Al-Mousa, Fawaz.
Affiliation
  • Michelangeli F; Chester Medical School, University of Chester, UK.
  • Mohammed NA; School of Biosciences, University of Birmingham, UK.
  • Jones B; School of Biosciences, University of Birmingham, UK.
  • Tairu M; Department of Biology, University of Duhok, Iraq.
  • Al-Mousa F; Chester Medical School, University of Chester, UK.
FEBS Open Bio ; 2024 Aug 13.
Article in En | MEDLINE | ID: mdl-39138623
ABSTRACT
Concerns regarding man-made organic chemicals pervading our ecosystem and having adverse and detrimental effects upon organisms, including man, have now been studied for several decades. Since the 1970s, some environmental pollutants were identified as having endocrine disrupting affects. These endocrine disrupting chemicals (EDC) were initially shown to have estrogenic or anti-estrogenic properties and some were also shown to bind to a variety of hormone receptors. However, since the 1990s it has also been identified that many of these EDC additionally, have the ability of causing abnormal alterations in Ca2+ signalling pathways (also commonly involved in hormone signalling), leading to exaggerated elevations in cytosolic [Ca2+] levels, that is known to cause activation of a number of cell death pathways. The major emphasis of this review is to present a personal perspective of the evidence for some types of EDC, specifically alkylphenols and brominated flame retardants (BFRs), causing direct effects on Ca2+ transporters (mainly the SERCA Ca2+ ATPases), culminating in acute cytotoxicity and cell death. Evidence is also presented to indicate that this Ca2+ATPase inhibition, which leads to abnormally elevated cytosolic [Ca2+], as well as a decreased luminal ER [Ca2+], which triggers the ER stress response, are both involved in acute cytotoxicity.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: FEBS Open Bio Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: FEBS Open Bio Year: 2024 Document type: Article Affiliation country: