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1.
Int J Dev Neurosci ; 69: 10-16, 2018 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-29908249

RESUMO

Axonal projection is controlled by discrete regions localized at the neuroepithelium, guiding the neurite growth during embryonic development. These regions exert their effect through the expression of a family of chemotropic molecules, which actively participate in the formation of neuronal connections of the central nervous system in vertebrates. Previous studies describe prosomere 1 (P1) as a possible organizer of axonal growth of the rostral rhombencephalon, contributing to the caudal projection of reticulospinal rhombencephalic neurons. This work studies the contribution of chemotropic signals from P1 or pretectal medial longitudinal fascicle (MLF) neurons upon the caudal projection of the interstitial nuclei of Cajal (INC). By using in ovo surgeries, retrograde axonal labeling, and immunohistochemical techniques, we were able to determine that the absence of P1 generates a failure in the INC caudal projection, while drastically diminishing the reticulospinal rhombencephalic neurons projections. The lack of INC projection significantly decreases the number of reticulospinal neurons projecting to the MLF. We found a 48.6% decrease in the projections to the MLF from the rostral and bulbar areas. Similarly, the observed decrease at prosomere 2 was 51.5%, with 61.8% and 32.4% for prosomeres 3 and 4, respectively; thus, constituting the most affected rostral regions. These results suggest the following possibilities: i, that the axons of the reticulospinal neurons employ the INC projection as a scaffold, fasciculating with this pioneer projection; and ii, that the P1 region, including pretectal MLF neurons, exerts a chemotropic effect upon the INC caudal projection. Nonetheless the identification of these chemotropic signals is still a pending task.


Assuntos
Diencéfalo/crescimento & desenvolvimento , Células Intersticiais de Cajal/fisiologia , Vias Neurais/crescimento & desenvolvimento , Vias Neurais/fisiologia , Animais , Axônios , Embrião de Galinha , Diencéfalo/fisiologia , Imuno-Histoquímica , Neuritos , Neurônios/fisiologia , Rombencéfalo/crescimento & desenvolvimento , Rombencéfalo/fisiologia
2.
Can J Microbiol ; 48(12): 1056-61, 2002 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-12619817

RESUMO

Acinetobacter calcoaceticus BD413 produces variable amounts of an exocellular lipase that becomes rapidly inactivated upon secretion. To achieve high yield and protect the enzyme, we assayed the addition of several inert compounds to cell-free supernatants, cell fractions, and whole cultures. Glass beads, poly(ethylene glycol) 600, Triton X-100, saccharose, gum arabic, and beta-cyclodextrin were among the compounds tested. beta-Cyclodextrin and gum arabic (and saccharose to a lesser extent) were effective enzyme stabilizers in cell-free supernatants, while gum arabic, glass beads, and Triton X-100 improved lipase secretion from cells, and, therefore, total lipase yield (30-50%, according to the additive). In whole cultures, beta-cyclodextrin was the most effective additive, particularly in combination with glass beads or gum arabic. Indeed, cultures containing beta-cyclodextrin plus gum arabic were able to maintain 95% (+/- 1.5%) of the initial lipase activity for more than 16 h, while control cultures with no additives maintained only 10% (+/- 4%) of the enzyme activity after the same period. In conclusion, the addition of inert compounds in cultures may be considered a useful approach for achieving increased yield and lipase stabilization, amenable for downstream processing.


Assuntos
Acinetobacter calcoaceticus/enzimologia , Microbiologia Industrial , Lipase/metabolismo , beta-Ciclodextrinas , Acinetobacter calcoaceticus/genética , Acinetobacter calcoaceticus/crescimento & desenvolvimento , Biomassa , Meios de Cultura , Ciclodextrinas/metabolismo , Estabilidade Enzimática , Vidro/química , Goma Arábica/metabolismo , Octoxinol/metabolismo , Polietilenoglicóis/metabolismo , Sacarose/metabolismo , Fatores de Tempo , beta-Galactosidase/análise
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