Toxic Effect of Cadmium, Lead, and Arsenic on the Sertoli Cell: Mechanisms of Damage Involved

DNA Cell Biol. 2018 Jul;37(7):600-608. doi: 10.1089/dna.2017.4081. Epub 2018 May 10.

Abstract

Over the past decades, an increase has been described in exposure to environmental toxins; consequently, a series of studies has been carried out with the aim of identifying problems associated with health. One of the main risk factors is exposure to heavy metals. The adverse effects that these compounds exert on health are quite complex and difficult to elucidate, in that they act at different levels and there are various signaling pathways that are implicated in the mechanisms of damage. The Sertoli cells plays a role of vital importance during the process of spermatogenesis, and it has been identified as one of the principal targets of heavy metals. In the present review, cadmium, lead, and arsenic are broached as altering the physiology of the Sertoli cells, citing mechanisms that have been cited in the literature.

Keywords: Sertoli cells; heavy metals; signaling pathways.

Publication types

  • Review

MeSH terms

  • Apoptosis / drug effects
  • Apoptosis / genetics
  • Arsenic / toxicity*
  • Cadmium / toxicity*
  • Environmental Pollutants / toxicity*
  • Follicle Stimulating Hormone / genetics
  • Follicle Stimulating Hormone / metabolism
  • Gene Expression Regulation / drug effects*
  • Humans
  • Lead / toxicity*
  • Luteinizing Hormone / genetics
  • Luteinizing Hormone / metabolism
  • Male
  • Sertoli Cells / cytology
  • Sertoli Cells / drug effects*
  • Sertoli Cells / metabolism
  • Signal Transduction
  • Spermatogenesis / drug effects
  • Spermatogenesis / genetics
  • Testosterone / antagonists & inhibitors
  • Testosterone / genetics
  • Testosterone / metabolism
  • p38 Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • p38 Mitogen-Activated Protein Kinases / genetics
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Environmental Pollutants
  • Cadmium
  • Lead
  • Testosterone
  • Luteinizing Hormone
  • Follicle Stimulating Hormone
  • p38 Mitogen-Activated Protein Kinases
  • Arsenic