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Hebbar S Lee E Manna M Steinert S Kumar GS Wenk M Wohland T Kraut R 《Journal of lipid research》2008,49(5):1077-1089
We have designed a tagged probe [sphingolipid binding domain (SBD)] to facilitate the tracking of intracellular movements of sphingolipids in living neuronal cells. SBD is a small peptide consisting of the SBD of the amyloid precursor protein. It can be conjugated to a fluorophore of choice and exogenously applied to cells, thus allowing for in vivo imaging. Here, we present evidence to describe the characteristics of the SBD association with the plasma membrane. Our experiments demonstrate that SBD binds to isolated raft fractions from human neuroblastomas and insect neuronal cells. In protein-lipid overlay experiments, SBD interacts with a subset of glycosphingolipids and sphingomyelin, consistent with its raft association in neurons. We also provide evidence that SBD is taken up by neuronal cells in a cholesterol- and sphingolipid-dependent manner via detergent-resistant microdomains. Furthermore, using fluorescence correlation spectroscopy to assay the mobility of SBD in live cells, we show that SBD's behavior at the plasma membrane is similar to that of the previously described raft marker cholera toxin B, displaying both a fast and a slow component. Our data suggest that fluorescently tagged SBD can be used to investigate the dynamic nature of glycosphingolipid-rich detergent-resistant microdomains that are cholesterol-dependent. 相似文献
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Lis1 and Ndel1 influence the timing of nuclear envelope breakdown in neural stem cells 总被引:3,自引:0,他引:3
Hebbar S Mesngon MT Guillotte AM Desai B Ayala R Smith DS 《The Journal of cell biology》2008,182(6):1063-1071
Lis1 and Ndel1 are essential for animal development. They interact directly with one another and with cytoplasmic dynein. The developing brain is especially sensitive to reduced Lis1 or Ndel1 levels, as both proteins influence spindle orientation, neural cell fate decisions, and neuronal migration. We report here that Lis1 and Ndel1 reduction in a mitotic cell line impairs prophase nuclear envelope (NE) invagination (PNEI). This dynein-dependent process facilitates NE breakdown (NEBD) and occurs before the establishment of the bipolar spindle. Ndel1 phosphorylation is important for this function, regulating binding to both Lis1 and dynein. Prophase cells in the ventricular zone (VZ) of embryonic day 13.5 Lis1+/− mouse brains show reduced PNEI, and the ratio of prophase to prometaphase cells is increased, suggesting an NEBD delay. Moreover, prophase cells in the VZ contain elevated levels of Ndel1 phosphorylated at a key cdk5 site. Our data suggest that a delay in NEBD in the VZ could contribute to developmental defects associated with Lis1–Ndel1 disruption. 相似文献
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K. P. Hebbar R. D. Lumsden S. M. Poch J. A. Lewis 《Applied microbiology and biotechnology》1997,48(6):714-719
Conditions for optimizing spore production, especially chlamydospores, by host-specific mycoherbicidal strains of Fusarium oxysporum causing vascular wilts in coca (Erythroxylum coca) and poppy (Papaver somniferum) were studied in 2.5-1 fermentors. The fermentor dissolved oxygen and pH had significant effects on the growth characteristics
of F. oxysporum strains. The effect of the fungal strain, however was not significant for most of the variables studied except for chlamydospore
formation. After 14 days of fermentation, the spore types produced were microconidia and chlamydospores, with very little
production of macroconidia. While the total viable counts were significantly higher under high than under low dissolved O2, the chlamydospore counts were significantly higher under low than under high dissolved O2. The percentage of chlamydospores obtained, as a proportion of total viable was significantly higher when the fermentor pH
was increased, than when it was not. Scaling-up the liquid fermentation to 20 l, yielded log10
c = 6.8 (where c = chlamydospores ml−1) after 14 days' fermentation, with biomass viable counts of log10
v∼8.0 (where v = viable counts g−1 air-dried biomass). A single-step liquid fermentation reported in this study increased chlamydospore yields and reduced the
time required for their production with techniques currently available from 5 weeks to less than 2 weeks.
Received: 24 April 1997 / Received revision: 6 August 1997 / Accepted: 29 August 1997 相似文献