RESUMO
Current limitations impeding on data reproducibility are often poor statistical design, underpowered studies, lack of robust data, lack of methodological detail, biased reporting and lack of open data sharing, coupled with wrong research incentives. To improve data reproducibility, robustness and quality for brain disease research, a Preclinical Data Forum Network was formed under the umbrella of the European College of Neuropsychopharmacology (ECNP). The goal of this network, members of which met for the first time in October 2014, is to establish a forum to collaborate in precompetitive space, to exchange and develop best practices, and to bring together the members from academia, pharmaceutical industry, publishers, journal editors, funding organizations, public/private partnerships and non-profit advocacy organizations. To address the most pertinent issues identified by the Network, it was decided to establish a data sharing platform that allows open exchange of information in the area of preclinical neuroscience and to develop an educational scientific program. It is also planned to reach out to other organizations to align initiatives to enhance efficiency, and to initiate activities to improve the clinical relevance of preclinical data. Those Network activities should contribute to scientific rigor and lead to robust and relevant translational data. Here we provide a synopsis of the proceedings from the inaugural meeting.
Assuntos
Pesquisa Biomédica/métodos , Avaliação Pré-Clínica de Medicamentos , Neurociências , Psicofarmacologia , Animais , Congressos como Assunto , Avaliação Pré-Clínica de Medicamentos/métodos , Europa (Continente) , Disseminação de Informação/métodos , Neurociências/métodos , Publicações Periódicas como Assunto , Guias de Prática Clínica como Assunto , Psicofarmacologia/métodos , Reprodutibilidade dos TestesRESUMO
We agree with the author that a quantitative analysis of the predictive nature of the metrics used in graduate student admissions is a worthy pursuit and value the sincere intentions behind the UCSF Tetrad study. However, these types of analyses would benefit from the same rigorous approaches that we employ in our other research endeavors. As UCSF Tetrad graduates with diverse careers in academia, medicine, industry, and publishing, we hope that the definition of success in graduate school can be as thoughtfully and scientifically examined as the measurements used to select the next young people to follow in our footsteps.
Assuntos
Educação de Pós-Graduação , Critérios de Admissão Escolar/tendências , Estudantes/estatística & dados numéricos , Feminino , Humanos , MasculinoRESUMO
Commissural axons in vertebrates and insects are initially attracted to the nervous system midline, but once they reach this intermediate target they undergo a dramatic switch, becoming responsive to repellent Slit proteins at the midline, which expel them onto the next leg of their trajectory. We have unexpectedly implicated a divergent member of the Robo family, Rig-1 (or Robo3), in preventing premature Slit sensitivity in mammals. Expression of Rig-1 protein by commissural axons is inversely correlated with Slit sensitivity. Removal of Rig-1 results in a total failure of commissural axons to cross. Genetic and in vitro analyses indicate that Rig-1 functions to repress Slit responsiveness similarly to Commissureless (Comm) in Drosophila. Unlike Comm, however, Rig-1 does not produce its effect by downregulating Robo receptors on precrossing commissural axon membranes. These results identify a mechanism for regulating Slit repulsion that helps choreograph the precise switch from attraction to repulsion at a key intermediate axonal target.
Assuntos
Diferenciação Celular/genética , Proteínas de Drosophila , Glicoproteínas/genética , Cones de Crescimento/metabolismo , Proteínas do Tecido Nervoso/genética , Malformações do Sistema Nervoso/genética , Receptores Imunológicos/deficiência , Medula Espinal/anormalidades , Animais , Células COS , Comunicação Celular/genética , Sinais (Psicologia) , Feto , Lateralidade Funcional/genética , Regulação da Expressão Gênica no Desenvolvimento/genética , Glicoproteínas/metabolismo , Cones de Crescimento/ultraestrutura , Proteínas de Membrana/genética , Proteínas de Membrana/metabolismo , Camundongos , Camundongos Knockout , Mutação/genética , Proteínas do Tecido Nervoso/metabolismo , Malformações do Sistema Nervoso/patologia , Ratos , Receptores de Superfície Celular , Receptores Imunológicos/genética , Medula Espinal/metabolismo , Medula Espinal/patologiaRESUMO
During development, retinal ganglion cell (RGC) axons either cross or avoid the midline at the optic chiasm. In Drosophila, the Slit protein regulates midline axon crossing through repulsion. To determine the role of Slit proteins in RGC axon guidance, we disrupted Slit1 and Slit2, two of three known mouse Slit genes. Mice defective in either gene alone exhibited few RGC axon guidance defects, but in double mutant mice a large additional chiasm developed anterior to the true chiasm, many retinal axons projected into the contralateral optic nerve, and some extended ectopically-dorsal and lateral to the chiasm. Our results indicate that Slit proteins repel retinal axons in vivo and cooperate to establish a corridor through which the axons are channeled, thereby helping define the site in the ventral diencephalon where the optic chiasm forms.
