liu.seSearch for publications in DiVA
Change search
ReferencesLink to record
Permanent link

Direct link
Autophagy of metallothioneins prevents TNF-induced oxidative stress and toxicity in hepatoma cells
University of Turin, Italy.
Linköping University, Department of Medical and Health Sciences, Division of Drug Research. Linköping University, Faculty of Medicine and Health Sciences.
University of Milano Bicocca, Italy.
University of Milano Bicocca, Italy.
Show others and affiliations
2015 (English)In: Autophagy, ISSN 1554-8627, E-ISSN 1554-8635, Vol. 11, no 12, 2184-2198 p.Article in journal (Refereed) PublishedText
Abstract [en]

Lysosomal membrane permeabilization (LMP) induced by oxidative stress has recently emerged as a prominent mechanism behind TNF cytotoxicity. This pathway relies on diffusion of hydrogen peroxide into lysosomes containing redox-active iron, accumulated by breakdown of iron-containing proteins and subcellular organelles. Upon oxidative lysosomal damage, LMP allows relocation to the cytoplasm of low mass iron and acidic hydrolases that contribute to DNA and mitochondrial damage, resulting in death by apoptosis or necrosis. Here we investigate the role of lysosomes and free iron in death of HTC cells, a rat hepatoma line, exposed to TNF following metallothionein (MT) upregulation. Iron-binding MT does not normally occur in HTC cells in significant amounts. Intracellular iron chelation attenuates TNF and cycloheximide (CHX)-induced LMP and cell death, demonstrating the critical role of this transition metal in mediating cytokine lethality. MT upregulation, combined with starvation-activated MT autophagy almost completely suppresses TNF and CHX toxicity, while impairment of both autophagy and MT upregulation by silencing of Atg7, and Mt1a and/or Mt2a, respectively, abrogates protection. Interestingly, MT upregulation by itself has little effect, while stimulated autophagy alone depresses cytokine toxicity to some degree. These results provide evidence that intralysosomal iron-catalyzed redox reactions play a key role in TNF and CHX-induced LMP and toxicity. The finding that chelation of intralysosomal iron achieved by autophagic delivery of MT, and to some degree probably of other iron-binding proteins as well, into the lysosomal compartment is highly protective provides a putative mechanism to explain autophagy-related suppression of death by TNF and CHX.

Place, publisher, year, edition, pages
TAYLOR & FRANCIS INC , 2015. Vol. 11, no 12, 2184-2198 p.
Keyword [en]
autophagy; cell death; hepatoma cells; iron; lysosomes; oxidative stress; TNF
National Category
Clinical Medicine
Identifiers
URN: urn:nbn:se:liu:diva-124499DOI: 10.1080/15548627.2015.1106662ISI: 000367806300006PubMedID: 26566051OAI: oai:DiVA.org:liu-124499DiVA: diva2:899657
Note

Funding Agencies|Ministero dellUniversita e della Ricerca; Universita degli Studi di Torino

Available from: 2016-02-02 Created: 2016-02-01 Last updated: 2016-02-02

Open Access in DiVA

No full text

Other links

Publisher's full textPubMed

Search in DiVA

By author/editor
Brunk, Ulf
By organisation
Division of Drug ResearchFaculty of Medicine and Health Sciences
In the same journal
Autophagy
Clinical Medicine

Search outside of DiVA

GoogleGoogle Scholar
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

Altmetric score

Total: 103 hits
ReferencesLink to record
Permanent link

Direct link