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1.
Chinese Medical Journal ; (24): 2543-2547, 2013.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-322165

RESUMO

<p><b>OBJECTIVE</b>To review the functions of these intracellular signals in their regulation of retinal ganglion cell (RGC) axon regeneration.</p><p><b>DATA SOURCES</b>Relevant articles published in English or Chinese from 1970 to present were selected from PubMed. Searches were made using the terms "intrinsic determinants, axon regeneration, RGC, optic nerve regeneration, and central nervous system axon regeneration."</p><p><b>STUDY SELECTION</b>Articles studying the mechanisms controlling RGC and central nervous system (CNS) axon regeneration were reviewed. Articles focusing on the intrinsic determinants of axon regeneration were selected.</p><p><b>RESULTS</b>Like other CNS neurons of mammals, RGCs undergo a developmental loss in their ability to grow axons as they mature, which is a critical contributing factor to the failure of nerve regeneration and repair after injury. This growth failure can be attributed, at least in part, by the induction of molecular programs preventing cellular overgrowth and termination of axonal growth upon maturation. Key intracellular signals and transcription factors, including B cell lymphoma/leukemia 2, cyclic adenine monophosphate, mammalian target of rapamycin, and Krüppel-like transcription factors, have been identified to play central roles in this process.</p><p><b>CONCLUSIONS</b>Intense effort and substantial progress have been made to identify the various intrinsic growth pathways that regulate RGC axon regeneration. More work is needed to elucidate the mechanisms of and the interrelationship between the actions of these factors and to successfully achieve regeneration and repair of the severed RGC axons.</p>


Assuntos
Animais , Humanos , AMP Cíclico , Fisiologia , Fatores de Transcrição Kruppel-Like , Fisiologia , Regeneração Nervosa , Nervo Óptico , Fisiologia , PTEN Fosfo-Hidrolase , Fisiologia , Proteínas Proto-Oncogênicas c-bcl-2 , Fisiologia , Proteína 3 Supressora da Sinalização de Citocinas , Proteínas Supressoras da Sinalização de Citocina , Fisiologia , Serina-Treonina Quinases TOR , Fisiologia
2.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-318876

RESUMO

<p><b>OBJECTIVE</b>To study the expression of green fluorescent protein gene and immunogenicity of ES312 vaccine both mediated by Starburst polyamidoamine (PAMAM) dendrimers in vivo.</p><p><b>METHODS</b>The complex of green fluorescent protein or ES312 gene with Starburst PAMAM dendrimers were injected intramuscularly in Balb/c mice. The expression level and distribution of green fluorescent protein gene was detected by flow cytometer, Western blot and immunofluorescence assay. The immunogenicity of DNA vaccine was detected by enzyme-linked immunosorbent assay.</p><p><b>RESULTS</b>The expression of green fluorescent protein mediated by Starburst PAMAM dendrimers was found in heart, liver, spleen, lung, kidney, brain and injected muscle from 2 hours to 7 days after the vaccination. The highest expression level of the gene was detected in kidney, as well as in endothelial cells. The antibody response evoked by the DNA vaccine carried by the Starburst PAMAM dendrimers was significantly higher than that of the net DNA vaccination. Vaccination with Starburst PAMAM dendrimers elicited higher expression level of the gene in brain and kidney than with the net gene itself.</p><p><b>CONCLUSION</b>As a novel non-viral DNA carrier with low self-antigenicity, Starburst PAMAM dendrimers have potential to mediate DNA transfer and expression in vivo.</p>


Assuntos
Animais , Feminino , Camundongos , Materiais Biocompatíveis , Farmacologia , Dendrímeros , Portadores de Fármacos , Farmacologia , Proteínas de Fluorescência Verde , Genética , Farmacocinética , Vacinas Antimaláricas , Alergia e Imunologia , Camundongos Endogâmicos BALB C , Poliaminas , Farmacologia , Vacinação , Vacinas de DNA , Alergia e Imunologia
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