RESUMO
@#The injury of peripheral nerve is generally accompanied with active regeneration responses. This paper is to summarize the molecular mechanism to promote the nerve regeneration, including various reactions of the neuronal body, nerve fiber, and regulatory molecules in the microenvironment, such as transcription factors, inflammatory mediators, nerve growth factors, etc., aiming to investigate the possible mechanism in the nerve regeneration after injury.
RESUMO
Objective To identify the cellular distribution of a my elin-associated protein (Nogo-A) in the central nervous system (CNS) of mice a nd explore its possible inhibition on the CNS axon regeneration after spinal cor d injury. Methods Brain, spinal cord, peripheral tissues and w eight-dropping injuried spinal cord from the adult C57BL/6 mice were studied. N ogo-A protein expression was localized immunohistochemically. Chick E12DRG neur ons were cultured and growth cone collapse assessed. Results N ogo-A protein expression detected was mainly in the oligodendrocyte cell body a nd the myelinated axons surrounded by cell processes rather than in the peripher al tissues. After spinal cord injury, Nogo-A was up-regulated at a moderate de gree in the area around the lesion. Chick E12 DRG growth cone collapse rate was as high as 70%, significantly higher than that in the blank control and vector control groups with a significant difference ( P