Lithium limits trimethyltin‐induced cytotoxicity and proinflammatory response in microglia without affecting the concurrent autophagy impairment. Issue 2 (25th May 2016)
- Record Type:
- Journal Article
- Title:
- Lithium limits trimethyltin‐induced cytotoxicity and proinflammatory response in microglia without affecting the concurrent autophagy impairment. Issue 2 (25th May 2016)
- Main Title:
- Lithium limits trimethyltin‐induced cytotoxicity and proinflammatory response in microglia without affecting the concurrent autophagy impairment
- Authors:
- Fabrizi, Cinzia
Pompili, Elena
Somma, Francesca
De Vito, Stefania
Ciraci, Viviana
Artico, Marco
Lenzi, Paola
Fornai, Francesco
Fumagalli, Lorenzo - Abstract:
- Abstract: Trimethyltin (TMT) is a highly toxic molecule present as an environmental contaminant causing neurodegeneration particularly of the limbic system both in humans and in rodents. We recently described the occurrence of impairment in the late stages of autophagy in TMT‐intoxicated astrocytes. Here we show that similarly to astrocytes also in microglia, TMT induces the precocious block of autophagy indicated by the accumulation of the autophagosome marker, microtubule associated protein light chain 3. Consistent with autophagy impairment we observe in TMT‐treated microglia the accumulation of p62/SQSTM1, a protein specifically degraded through this pathway. Lithium has been proved effective in limiting neurodegenerations and, in particular, in ameliorating symptoms of TMT intoxication in rodents. In our in vitro model, lithium displays a pro‐survival and anti‐inflammatory action reducing both cell death and the proinflammatory response of TMT‐treated microglia. In particular, lithium exerts these activities without reducing TMT‐induced accumulation of light chain 3 protein. In fact, the autophagic block imposed by TMT is unaffected by lithium administration. These results are of interest as defects in the execution of autophagy are frequently observed in neurodegenerative diseases and lithium is considered a promising therapeutic agent for these pathologies. Thus, it is relevant that this cation can still maintain its pro‐survival and anti‐inflammatory role inAbstract: Trimethyltin (TMT) is a highly toxic molecule present as an environmental contaminant causing neurodegeneration particularly of the limbic system both in humans and in rodents. We recently described the occurrence of impairment in the late stages of autophagy in TMT‐intoxicated astrocytes. Here we show that similarly to astrocytes also in microglia, TMT induces the precocious block of autophagy indicated by the accumulation of the autophagosome marker, microtubule associated protein light chain 3. Consistent with autophagy impairment we observe in TMT‐treated microglia the accumulation of p62/SQSTM1, a protein specifically degraded through this pathway. Lithium has been proved effective in limiting neurodegenerations and, in particular, in ameliorating symptoms of TMT intoxication in rodents. In our in vitro model, lithium displays a pro‐survival and anti‐inflammatory action reducing both cell death and the proinflammatory response of TMT‐treated microglia. In particular, lithium exerts these activities without reducing TMT‐induced accumulation of light chain 3 protein. In fact, the autophagic block imposed by TMT is unaffected by lithium administration. These results are of interest as defects in the execution of autophagy are frequently observed in neurodegenerative diseases and lithium is considered a promising therapeutic agent for these pathologies. Thus, it is relevant that this cation can still maintain its pro‐survival and anti‐inflammatory role in conditions of autophagy block. Copyright © 2016 John Wiley & Sons, Ltd. Abstract : Trimethyltin (TMT) is a highly toxic molecule present as an environmental contaminant causing neurodegeneration particularly of the limbic systemboth in humans and in rodents. We recently described the occurrence of impairment in the late stages of autophagy in TMT‐intoxicated astrocytes. Here we show that similarly to astrocytes also in microglia, TMT induces the precocious block of autophagy indicated by the accumulation of the autophagosome marker, microtubule associated protein light chain 3. … (more)
- Is Part Of:
- Journal of applied toxicology. Volume 37:Issue 2(2017)
- Journal:
- Journal of applied toxicology
- Issue:
- Volume 37:Issue 2(2017)
- Issue Display:
- Volume 37, Issue 2 (2017)
- Year:
- 2017
- Volume:
- 37
- Issue:
- 2
- Issue Sort Value:
- 2017-0037-0002-0000
- Page Start:
- 207
- Page End:
- 213
- Publication Date:
- 2016-05-25
- Subjects:
- microglia -- trimethyltin -- autophagy -- neurodegeneration -- neuroinflammation
Toxicology -- Periodicals
Industrial toxicology -- Periodicals
Environmentally induced diseases -- Periodicals
Toxicology -- Periodicals
615.9005 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-1263/issues ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jat.3344 ↗
- Languages:
- English
- ISSNs:
- 0260-437X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4947.130000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1219.xml