Neuroprotective fragment C of tetanus toxin modulates IL-6 in an ALS mouse model

Autor: Rosario Osta, Laura Moreno-Martínez, Pilar Zaragoza, José Aguilera, Miriam de la Torre, Ana C. Calvo, María Jesús Muñoz
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Male
amyotrophic lateral sclerosis
Inflammasomes
Health
Toxicology and Mutagenesis

Anti-Inflammatory Agents
lcsh:Medicine
Nod
Pharmacology
Toxicology
Pyrin domain
Superoxide Dismutase-1
0302 clinical medicine
Macrophage inflammatory protein
0303 health sciences
biology
Chemistry
Communication
Caspase 1
Interleukin
Neuroprotective Agents
Spinal Cord
Female
Inflammation Mediators
medicine.symptom
TTC
Down-Regulation
Mice
Transgenic

Inflammation
Neuroprotection
SOD1G93A mouse model
03 medical and health sciences
Tetanus Toxin
NLR Family
Pyrin Domain-Containing 3 Protein

medicine
Animals
cardiovascular diseases
Muscle
Skeletal

Interleukin 6
Neuroinflammation
030304 developmental biology
Interleukin-6
lcsh:R
Amyotrophic lateral sclerosis
Peptide Fragments
Mice
Inbred C57BL

Disease Models
Animal

inflammation
biology.protein
030217 neurology & neurosurgery
Zdroj: Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Zaguán: Repositorio Digital de la Universidad de Zaragoza
Universidad de Zaragoza
Toxins
Toxins, Vol 12, Iss 330, p 330 (2020)
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
Popis: Neuroinflammation plays a significant role in amyotrophic lateral sclerosis (ALS) pathology, leading to the development of therapies targeting inflammation in recent years. Our group has studied the tetanus toxin C-terminal fragment (TTC) as a therapeutic molecule, showing neuroprotective properties in the SOD1G93A mouse model. However, it is unknown whether TTC could have some effect on inflammation. The objective of this study was to assess the effect of TTC on the regulation of inflammatory mediators to elucidate its potential role in modulating inflammation occurring in ALS. After TTC treatment in SOD1G93A mice, levels of eotaxin-1, interleukin (IL)-2, IL-6 and macrophage inflammatory protein (MIP)-1 alpha (α) and galectin-1 were analyzed by immunoassays in plasma samples, whilst protein expression of caspase-1, IL-1β, IL-6 and NOD-, LRR- and pyrin domain-containing protein 3 (NLRP3) was measured in the spinal cord, extensor digitorum longus (EDL) muscle and soleus (SOL) muscle. The results showed reduced levels of IL-6 in spinal cord, EDL and SOL in treated SOD1G93A mice. In addition, TTC showed a different role in the modulation of NLRP3 and caspase-1 depending on the tissue analyzed. In conclusion, our results suggest that TTC could have a potential anti-inflammatory effect by reducing IL-6 levels in tissues drastically affected by the disease. However, further research is needed to study more in depth the anti-inflammatory effect of TTC in ALS.
Databáze: OpenAIRE