2009
DOI: 10.1194/jlr.m800660-jlr200
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Depletion of phosphatidylcholine affects endoplasmic reticulum morphology and protein traffic at the Golgi complex

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Cited by 55 publications
(42 citation statements)
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“…Alternatively, we regulated DAG by knocking down CTP:phosphocholine cytidylyltransferase, the regulatory enzyme for PC synthesis, for a short time. Interestingly, a temperature shift to 40°C in CHO-MT58 for longer times than those used here leads to a PC mass reduction or TAG increase (40,44). In the first case, the authors observed a decrease in secretion and suggested that PC was needed for protein transport at the Golgi.…”
Section: Discussionmentioning
confidence: 73%
“…Alternatively, we regulated DAG by knocking down CTP:phosphocholine cytidylyltransferase, the regulatory enzyme for PC synthesis, for a short time. Interestingly, a temperature shift to 40°C in CHO-MT58 for longer times than those used here leads to a PC mass reduction or TAG increase (40,44). In the first case, the authors observed a decrease in secretion and suggested that PC was needed for protein transport at the Golgi.…”
Section: Discussionmentioning
confidence: 73%
“…Manipulation of the CDP-choline pathway with specific enzyme inhibitors, metabolites, or temperature-induced destabilization of CCTa in CHO MT-58 cells was used to vary cellular DAG content. The latter was positively correlated with modulation of vesicular transport of select proteins from Golgi to the surface membrane, but did not affect ER to Golgi or lysosome to PM traffic [9,115]. Based on the yeast secretion model systems, it was suggested that high levels of PC, induced by a PC turnover defect, trigger secretory impairment [116].…”
Section: The Role Of Cct In Vesicular Transportmentioning
confidence: 97%
“…Denuded oocytes were then washed again in PBS and fixed in 4% (v/v) paraformaldehyde (PF; Electron Microscopy Sciences, Hatfield, PA) at 378C for 1 h and stored in 1% (v/v) PF at 48C for a maximum of 1 wk. Oocytes were washed twice in PBS with 0.3% (w/v) polyvinylpyrrolidone (PVP), permeabilized for 30 min in PBS with 0.1% (w/v) saponin (PBS-S; Riedel-de Haën, Seelze, Germany) and 0.1 M glycin (Merck) and washed in PBS-S. To determine the maturational stage, oocytes were stained with 10 lg/ml TO-PRO-3 (Molecular Probes, Eugene, OR) for 20 min and subsequently three times washed in PBS-S. After this, neutral lipids in lipid droplets were stained according to a modified protocol of Chinese hamster ovary cells [30]. Lipid droplets were stained with the specific neutral lipid stain BODIPY 493/503 (Molecular Probes) in PBS (20 lg/ml, 1 h), and oocytes were washed three times in PBS with 3 mg/ml PVP.…”
Section: Lipid Droplet Staining Of Oocytesmentioning
confidence: 99%