Effects of bile salts on human erythrocytes. Plasma membrane vesiculation, phospholipid solubilization and their possible relationships to bile secretion
Biochimica et Biophysica Acta (BBA) - Biomembranes, ISSN: 0005-2736, Vol: 509, Issue: 1, Page: 33-47
1978
- 80Citations
- 4Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations80
- Citation Indexes80
- 80
- CrossRef66
- Captures4
- Readers4
Article Description
Glycocholate removed approximately 25% of the membrane acetylcholinesterase and 10% of the membrane phospholipid from intact human erythrocytes prior to the onset of cell lysis. At low concentrations (up to 6 mM), glycocholate caused human erythrocytes to become echinocytic and to pinch off microvesicles, whereas at higher concentrations glycocholate also specifically released components from the outer leaflet of the plasma membrane in a ‘soluble’ form (as defined by their presence in a 150 000 × g /60 min supernatant) and caused the cells to become stomatocytic. Whilst the phospholipid profile of the ‘soluble’ material differed from that of the whole membrane, the profile of the microvesicle fraction was similar. The microvesicles were depleted in several membrane proteins with respect to phospholipids. These observations are discussed in relation to the possible role of bile salts in the origins of biliary phospholipid and protein.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/0005273678900056; http://dx.doi.org/10.1016/0005-2736(78)90005-6; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0018097703&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/647007; https://linkinghub.elsevier.com/retrieve/pii/0005273678900056; http://dx.doi.org/10.1016/0005-2736%2878%2990005-6; https://dx.doi.org/10.1016/0005-2736%2878%2990005-6
Elsevier BV
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