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Zawartość zarchiwizowana w dniu 2024-05-30

The role of JNK/c-Jun pathway in axonal damage and neuronal regeneration

Cel

Interruption of axons results in a characteristic reaction of the injured neuron, the so-called axonal response, which aims to induce axon elongation and to achieve a re-construction of effective synapses. Nerve fiber transection elicits a complex neuronal response that leaves neurons poised between death and regeneration. Although the signals underlying this dichotomy are not fully understood, some are mediated by the induction of immediate-early transcription factors of the AP-1 family, a key regulator in crucial cellular events. AP-1 activity is regulated, in part, by the phosphorylation of its c-Jun component by the Jun N-terminal Kinases (JNKs). Recent work has confirmed the notion that c-Jun functions as the trigger of the axonal response during neuronal regeneration in the CNS and strongly supports the perception of c-Jun action as a “double-edged sword” promoting post-traumatic neuronal cell death as well as axonal regeneration. The goal of this project is to better understand the function of the JNK/c-Jun pathway during neuronal regeneration by generating and employing gain and loss-of-function transgenic mice models and to clarify the role of JNKs/c-Jun phosphorylation in the neuronal response to axonal damage. The assessment of the reinnervation after injury in these transgenic lines will use suitable regeneration paradigms. We are also interested in identifying new JNK/c-Jun mediators that could play a role in the axonal response to injury. Thus, future perspectives towards the strengthening of European potential research could derive from this study. This project integrates well in the FP7 program, and will applicate knowledge and biotechnology for health. The accomplishment of the project would contribute significantly to the acquisition of new relevant data on JNK functions in neuronal death and axonal regeneration, which is indispensable to predict the outcome of JNK/c-Jun system inhibition as a putative therapeutical strategy.

Zaproszenie do składania wniosków

FP7-PEOPLE-IEF-2008
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Koordynator

CANCER RESEARCH UK LBG
Wkład UE
€ 171 867,63
Adres
2 Redman Place
E20 1JQ LONDON
Zjednoczone Królestwo

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Region
London Inner London — West Camden and City of London
Rodzaj działalności
Research Organisations
Kontakt administracyjny
Holly Elphinstone (Ms.)
Linki
Koszt całkowity
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