Unknown

Dataset Information

0

Thiazolidinediones promote axonal growth through the activation of the JNK pathway.


ABSTRACT: The axon is a neuronal process involved in protein transport, synaptic plasticity, and neural regeneration. It has been suggested that their structure and function are profoundly impaired in neurodegenerative diseases. Previous evidence suggest that Peroxisome Proliferator-Activated Receptors-? (PPAR? promote neuronal differentiation on various neuronal cell types. In addition, we demonstrated that activation of PPAR?by thiazolidinediones (TZDs) drugs that selectively activate PPAR? prevent neurite loss and axonal damage induced by amyloid-? (A?). However, the potential role of TZDs in axonal elongation and neuronal polarity has not been explored. We report here that the activation of PPAR? by TZDs promoted axon elongation in primary hippocampal neurons. Treatments with different TZDs significantly increased axonal growth and branching area, but no significant effects were observed in neurite elongation compared to untreated neurons. Treatment with PPAR? antagonist (GW 9662) prevented TZDs-induced axonal growth. Recently, it has been suggested that the c-Jun N-terminal kinase (JNK) plays an important role regulating axonal growth and neuronal polarity. Interestingly, in our studies, treatment with TZDs induced activation of the JNK pathway, and the pharmacological blockage of this pathway prevented axon elongation induced by TZDs. Altogether, these results indicate that activation of JNK induced by PPAR?activators stimulates axonal growth and accelerates neuronal polarity. These novel findings may contribute to the understanding of the effects of PPAR? on neuronal differentiation and validate the use of PPAR? activators as therapeutic agents in neurodegenerative diseases.

SUBMITTER: Quintanilla RA 

PROVIDER: S-EPMC3669289 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature

altmetric image

Publications

Thiazolidinediones promote axonal growth through the activation of the JNK pathway.

Quintanilla Rodrigo A RA   Godoy Juan A JA   Alfaro Ivan I   Cabezas Deny D   von Bernhardi Rommy R   Bronfman Miguel M   Inestrosa Nibaldo C NC  

PloS one 20130531 5


The axon is a neuronal process involved in protein transport, synaptic plasticity, and neural regeneration. It has been suggested that their structure and function are profoundly impaired in neurodegenerative diseases. Previous evidence suggest that Peroxisome Proliferator-Activated Receptors-γ (PPARγ promote neuronal differentiation on various neuronal cell types. In addition, we demonstrated that activation of PPARγby thiazolidinediones (TZDs) drugs that selectively activate PPARγ prevent neur  ...[more]

Similar Datasets

| S-EPMC5809495 | biostudies-literature
| S-EPMC7396445 | biostudies-literature
| S-EPMC3535671 | biostudies-literature
| S-EPMC8978515 | biostudies-literature
| S-EPMC8016927 | biostudies-literature
| S-EPMC3395089 | biostudies-literature
| S-EPMC4823078 | biostudies-literature
| S-EPMC8315012 | biostudies-literature
| S-EPMC2695006 | biostudies-literature