2008
DOI: 10.1007/s10565-008-9058-x
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Cardosins improve neuronal regeneration after cell disruption: a comparative expression study

Abstract: The establishment of primary cell cultures is invaluable for studying cell and molecular biological questions. Although primary cell cultures more closely resemble and function like in the native environment, during the culture establishment the cells undergo several changes including the damage sustained during their removal from original tissue. The resultant cells have to rebalance the expression of their processing molecules to ascertain matrix signalling that ensure cell adaptation and consequent prolifer… Show more

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Cited by 5 publications
(4 citation statements)
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“…Neurons treated with cardosins exhibit normal morphology and function when compared to cultures prepared with the widely used trypsin-dissociation method (Duarte et al, 2007). Furthermore, use of cardosins resulted in an improvement of neuronal regeneration at an early stages of culture after cell dissociation (Duarte et al, 2009).…”
Section: Biotechnological and Biomedical Applicationsmentioning
confidence: 99%
“…Neurons treated with cardosins exhibit normal morphology and function when compared to cultures prepared with the widely used trypsin-dissociation method (Duarte et al, 2007). Furthermore, use of cardosins resulted in an improvement of neuronal regeneration at an early stages of culture after cell dissociation (Duarte et al, 2009).…”
Section: Biotechnological and Biomedical Applicationsmentioning
confidence: 99%
“…Gelatinolytic activity was assessed by zymography, as described previously [ 48 ], with slight modifications. Gelatin [1% ( w / v )] was used.…”
Section: Methodsmentioning
confidence: 99%
“…Gelatinolytic and caseinolytic activity was assessed by zymography, using 1% (w/v) gelatine or 1% (w/v) casein, as described previously ( Duarte et al, 2009 ; Esteves et al, 2014 ), with slight modifications. After electrophoresis, the gel was incubated overnight, at room temperature, in 1.5 mM Tris, pH 8.8, 1 M NaCl, 1 M CaCl 2 , 2 mM ZnCl 2 , pH 7.4, stained with Coomassie Brilliant Blue R-250 [(in 50% ethanol (v/v), 10% acetic acid (v/v)] and destained with 25% ethanol (v/v), 5% acetic acid (bgv/v).…”
Section: Methodsmentioning
confidence: 99%