Cited by 35Cell death mechanisms and regulationCarcinogens and Genotoxicity AssessmentBioactive Compounds and Antitumor Agents

Involvement of cathepsin B in mitochondrial apoptosis by p-phenylenediamine under ambient UV radiation

Goyal, Shruti, Amar, Saroj Kumar, Dubey, Divya, Pal, Manish Kumar, Singh, Jyoti, Verma, Ankit, Kushwaha, Hari Narayan, Ray, Ratan Singh·2015·Journal of Hazardous Materials

Abstract

Paraphenylenediamine (PPD), a derivative of paranitroaniline has been most commonly used as an ingredient of oxidative hair dye and permanent tattoos. We have studied the phototoxic potential of PPD under ambient ultraviolet radiation. PPD is photodegraded and form a novel photoproduct under UV A exposure. PPD shows a concentration dependent decrease in cell viability of human Keratinocyte cells (HaCaT) through MTT and NRU test. Significant intracellular ROS generation was measured by DCFDA assay. It caused an oxidative DNA damage via single stranded DNA breaks, micronuclei and CPD formation. Both lysosome and mitochondria is main target for PPD induced apoptosis which was proved through lysosomal destabilization and release of cathepsin B by immunofluorescence, real time PCR and western blot analysis. Cathepsin B process BID to active tBID which induces the release of cytochrome C from mitochondria. Mitochondrial depolarization was reported through transmission electron microscopy. The cathepsin inhibitor reduced the release of cytochrome C in PPD treated cells. Thus study suggests that PPD leads to apoptosis via the involvement of lysosome and mitochondria both under ambient UV radiation. Therefore, photosensitizing nature of hair dye ingredients should be tested before coming to market as a cosmetic product for the safety of human beings.

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Crossref · 10.1016/j.jhazmat.2015.07.032

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  • After ultraviolet radiation exposure, paraphenylenediamine and 2-Amino-3-hydroxypyridine become photosensitized and form toxic photoproducts, which causes genetic damage and apoptosis in skin cells.

    “According to studies, after ultraviolet radiation exposure, these ingredients become photosensitized and form toxic photoproducts, which causes genetic damage and apoptosis in skin cells”

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Authors
Goyal, S., Amar, S. K., Dubey, D., Pal, M. K., Singh, J., Verma, A., Kushwaha, H. N., & Ray, R. S.
Affiliations
Indian Institute of Toxicology Research (IN)
Corresponding author
Ray, Ratan Singh
Venue
Journal of Hazardous Materials
Publisher
Elsevier BV
Published
2015-12
Volume
300
Pages
415-425
ISSN
0304-3894 (ISSN-L)
OpenAlex
W885216574
Cited by
35
References
3
Citations by year
2026: 1 · 2023: 6 · 2022: 2 · 2021: 6 · 2020: 2 · 2019: 3 · 2018: 5 · 2017: 4 · 2016: 5 · 2015: 1
FWCI
2.17
Type
journal article
Language
en
Update notices
erratum (2019-11-05)
Open access
closed
Locations
  • Journal of Hazardous Materials (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • CSIR-Network project INDEPTH BSC011
  • University Grant Commission, New Delhi, India
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Carcinogens and Genotoxicity Assessment
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Toxicology › Bioactive Compounds and Antitumor Agents
Keywords
p-phenylenediamine, hair dyes, UV-A radiation, cathepsin B, mitochondrial apoptosis, reactive oxygen species, oxidative DNA damage, cytochrome c release, Bid cleavage, mitochondrial depolarization, HaCaT keratinocytes, photoproducts, cosmetic safety
MeSH terms
Antioxidants, Cathepsin B, Cell Cycle, Cell Line, DNA Damage, Humans, Lysosomes, Mitochondria, Phenylenediamines, Ultraviolet Rays, Micronucleus Tests, Keratinocytes, Apoptosis, Reactive Oxygen Species, Membrane Potential, Mitochondrial

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