<p>Lysates from LPS-activated astrocytes were incubated with exogenous MBP, then subjected to SDS-PAGE as described in text. As controls, MBP was incubated without cell lysate (MBP control) or with lysate from unactivated astrocytes (CTRL). A, Calcium dependency of MBP degradation. B, Substrate specificity of proteolytic activity present in LPS-activated lysates towards MBP. C, Dose-dependent degradation of MBP by LPS-activated lysates from astrocytes after incubation at 37°C for 24 h. D, Time-course of the MBP degradation by 30 μl of LPS-activated lysate. In the lower part of C and D MBP degradation is expressed as optical density (OD × mm<sup>2</sup>) as calculated by densitometrical analysis of gel.</p
<p><b>A.</b> Degradation of ΔPrPs by lysosomal and proteasomal systems. (Left) N2a cells transiently...
Astrocytic glycogen degradation is an important factor in metabolic support of brain function, parti...
<p>(A) Nuclear and cytoplasmic protein fractions of astrocytes were analyzed by Western blot. The in...
<p>30 µl of lysates (A) or 50 µl of supernatants (B) from LPS-activated astrocytes were incubated fo...
<p>Primary astrocytes (1×10<sup>5</sup> cells/ml), incubated in serum-free DMEM, were treated with I...
<p>A. Primary astrocyte cultures. Over 99% cells were labeled with GFAP. B. Stat3 distribution in as...
<p>(<b>A</b>) PKA activity in cerebellar astrocytes treated with different concentrations of H89 for...
<p>(<b>A</b>) Astrocytes were treated with 2 µg/ml of LPS for 0, 6, 8, 10, 12, 14, or 18 h, then who...
<p>(<b>A</b>) Astrocytes were pretreated with 2 µg/ml LPS (<b>LPS</b>) for 8 h followed by treatment...
<p>(A) MBP surface binding on neurons after 30-min pre-incubation in ECS at pH 7.4 or pH 10.8 (equal...
<p>Primary astrocytes (1×10<sup>5</sup> cells/ml), incubated in serum-free DMEM, were treated with M...
<p><i>A,</i> Astrocytes were transiently transfected with pEGFP or pEGFP-UBB+1. After 72 hrs, cells ...
<p>Primary astrocytes (1×10<sup>5</sup> cells/ml), were activated with LPS (10 μg/ml) and simultaneo...
<p>(<b>A</b>) Astrocytes were treated with 0.05% DMSO for 8 h (<b>Cont</b>), with 5 µM MG132 for 4, ...
<p><b>A.</b> Quantitative analysis of ATP production in MB treated astrocytes at 60 min after reoxyg...
<p><b>A.</b> Degradation of ΔPrPs by lysosomal and proteasomal systems. (Left) N2a cells transiently...
Astrocytic glycogen degradation is an important factor in metabolic support of brain function, parti...
<p>(A) Nuclear and cytoplasmic protein fractions of astrocytes were analyzed by Western blot. The in...
<p>30 µl of lysates (A) or 50 µl of supernatants (B) from LPS-activated astrocytes were incubated fo...
<p>Primary astrocytes (1×10<sup>5</sup> cells/ml), incubated in serum-free DMEM, were treated with I...
<p>A. Primary astrocyte cultures. Over 99% cells were labeled with GFAP. B. Stat3 distribution in as...
<p>(<b>A</b>) PKA activity in cerebellar astrocytes treated with different concentrations of H89 for...
<p>(<b>A</b>) Astrocytes were treated with 2 µg/ml of LPS for 0, 6, 8, 10, 12, 14, or 18 h, then who...
<p>(<b>A</b>) Astrocytes were pretreated with 2 µg/ml LPS (<b>LPS</b>) for 8 h followed by treatment...
<p>(A) MBP surface binding on neurons after 30-min pre-incubation in ECS at pH 7.4 or pH 10.8 (equal...
<p>Primary astrocytes (1×10<sup>5</sup> cells/ml), incubated in serum-free DMEM, were treated with M...
<p><i>A,</i> Astrocytes were transiently transfected with pEGFP or pEGFP-UBB+1. After 72 hrs, cells ...
<p>Primary astrocytes (1×10<sup>5</sup> cells/ml), were activated with LPS (10 μg/ml) and simultaneo...
<p>(<b>A</b>) Astrocytes were treated with 0.05% DMSO for 8 h (<b>Cont</b>), with 5 µM MG132 for 4, ...
<p><b>A.</b> Quantitative analysis of ATP production in MB treated astrocytes at 60 min after reoxyg...
<p><b>A.</b> Degradation of ΔPrPs by lysosomal and proteasomal systems. (Left) N2a cells transiently...
Astrocytic glycogen degradation is an important factor in metabolic support of brain function, parti...
<p>(A) Nuclear and cytoplasmic protein fractions of astrocytes were analyzed by Western blot. The in...