Beta-Interferon-Induced Time-Dependent Changes in the Plasma Membrane Lipid Bilayer of Cultured Cells

1981 ◽  
Vol 1 (4) ◽  
pp. 613-620 ◽  
Author(s):  
LAWRENCE M. PFEFFER ◽  
FRANK R. LANDSBERGER ◽  
IGOR TAMM
Keyword(s):  
Plasma Membrane ◽  
Lipid Bilayer ◽  
Cultured Cells ◽  
Membrane Lipid ◽  
Time Dependent ◽  
Beta Interferon ◽  
Plasma Membrane Lipid ◽  
Membrane Lipid Bilayer

scholarly journals Transport of (Glyco)Sphingolipids in and Between Cellular Membranes; Multidrug Transporters and Lateral Domains

1999 ◽  
Vol 19 (4) ◽  
pp. 327-333 ◽  
Author(s):  
Gerrit van Meer ◽  
Dan Sillence ◽  
Hein Sprong ◽  
Nanette Kälin ◽  
René Raggers
Keyword(s):  
Plasma Membrane ◽  
Cancer Cells ◽  
Lipid Bilayer ◽  
Membrane Lipid ◽  
Golgi Membrane ◽  
Cellular Membranes ◽  
Multidrug Transporters ◽  
Outer Leaflet ◽  
Plasma Membrane Lipid ◽  
Membrane Lipid Bilayer

Sphingolipids are highly enriched in the outer leaflet of the plasma membrane lipid bilayer. However, the first glycolipid, glucosylceramide, is synthesized in the opposite, cytosolic leaflet of the Golgi membrane. This has led us to experiments which suggest that the level of glucosylceramide in the cytosolic surface is carefully regulated both by the balance between synthesis and hydrolysis and by transport away from this surface through translocators, multidrug transporters, the same molecules that make cancer cells resistant to chemotherapy. Our data suggest a role for newly synthesized glucosylceramide not only in the formation of domains in the luminal leaflet of the Golgi but also on the cytosolic surface of this organelle.

Time-Course of Changes in the Plasma–Membrane Lipid Bilayer and Cellular Ultrastructure Induced by Tumour Necrosis Factor-α in K 562 and Daudi Cells

1995 ◽  
Vol 23 (4) ◽  
pp. 254-263 ◽  
Author(s):  
M Marutaka ◽  
H Iwagaki ◽  
K Mizukawa ◽  
N Tanaka ◽  
K Orita
Keyword(s):  
Plasma Membrane ◽  
Cell Membrane ◽  
Membrane Fluidity ◽  
Time Course ◽  
Membrane Lipid ◽  
Plasma Membrane Lipid ◽  
Membrane Lipid Bilayer ◽  
Cell Membrane Fluidity ◽  
K 562 Cells ◽  
Factor Α

The time-course of changes in the plasma-membrane lipid bilayer induced by tumour necrosis factor-α (TNF) were investigated in cultured cells using spin-label electron-spin-resonance techniques. Treatment of K 562 cells, a human chronic myelocytic leukaemia cell line, in suspension culture with TNF for up to 6 h caused an initial increase in cell-membrane fluidity, which returned to the control level after 12 h of treatment. After 24 h of treatment, the cell-membrane fluidity had decreased and this decrease was maintained after 48 h of treatment. In Daudi cells, a human malignant lymphoma cell line, TNF, did not induce any changes in cell-membrane fluidity, indicating that the effect of TNF on membrane structure is cell-specific. The early and transient change in membrane fluidity in K 562 cells is probably related to signal generation, while the later, persistent change may reflect the phenotype of TNF-treated cells, in particular, changes in the plasma membrane-cytoplasmic complex. Histochemical electron microscopic studies indicated that the membrane fluidity changes induced by TNF have an ultrastructural correlate.

scholarly journals Kinetic Study of 17α-Estradiol Activity in Comparison with 17β-Estradiol and 17α-Ethynylestradiol

Catalysts ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 634
Author(s):  
Tereza Bosakova ◽  
Antonin Tockstein ◽  
Zuzana Bosakova ◽  
Katerina Komrskova
Keyword(s):  
Experimental Data ◽  
Plasma Membrane ◽  
Kinetic Model ◽  
Critical Level ◽  
Membrane Lipid ◽  
Molar Ratio ◽  
Plasma Membrane Lipid ◽  
Membrane Lipid Bilayer ◽  
17Β Estradiol ◽  
New Interactions

17α-estradiol (αE2), an endogenous stereoisomer of the hormone 17β-estradiol (E2), is capable of binding to estrogen receptors (ER). We aimed to mathematically describe, using experimental data, the possible interactions between αE2 and sperm ER during the process of sperm capacitation and to develop a kinetic model. The goal was to compare the suggested kinetic model with previously published results of ER interactions with E2 and 17α-ethynylestradiol (EE2). The HPLC-MS/MS method was developed to monitor the changes of αE2 concentration during capacitation. The calculated relative concentrations Bt were used for kinetic analysis. Rate constants k and molar ratio n were optimized and used for the construction of theoretical B(t) curves. Modifications in αE2–ER interactions were discovered during comparison with models for E2 and EE2. These new interactions displayed autocatalytic formation of an unstable adduct between the hormone and the cytoplasmic receptors. αE2 accumulates between the plasma membrane lipid bilayer with increasing potential, and when the critical level is reached, αE2 penetrates through the inner layer of the plasma membrane into the cytoplasm. It then rapidly reacts with the ER and creates an unstable adduct. The revealed dynamics of αE2–ER action may contribute to understanding tissue rejuvenation and the cancer-related physiology of αE2 signaling.

Dietary fat ratios and liver plasma membrane lipid composition

Lipids ◽  
1988 ◽  
Vol 23 (9) ◽  
pp. 829-833 ◽  
Author(s):  
Michael W. Hamm ◽  
Anna Sekowski ◽  
Roni Ephrat
Keyword(s):  
Plasma Membrane ◽  
Lipid Composition ◽  
Dietary Fat ◽  
Membrane Lipid ◽  
Membrane Lipid Composition ◽  
Liver Plasma Membrane ◽  
Plasma Membrane Lipid

scholarly journals PHLIP ARG-Mutant Interactions with the Membrane Lipid Bilayer

2021 ◽  
Vol 120 (3) ◽  
pp. 232a
Author(s):  
Hannah M. Visca ◽  
Oleg A. Andreev ◽  
Yana K. Reshetnyak
Keyword(s):  
Lipid Bilayer ◽  
Membrane Lipid ◽  
Membrane Lipid Bilayer

Plasma membrane lipid packing and leukocyte function-associated antigen-1-dependent aggregation of lymphocytes

1993 ◽  
Vol 156 (1) ◽  
pp. 182-188 ◽  
Author(s):  
Douglas M. Smith ◽  
Patrick L. Williamson ◽  
Robert A. Schlegel
Keyword(s):  
Plasma Membrane ◽  
Membrane Lipid ◽  
Lipid Packing ◽  
Plasma Membrane Lipid ◽  
Leukocyte Function

Alterations in plasma membrane lipid organization during lymphocyte differentiation

1986 ◽  
Vol 126 (3) ◽  
pp. 379-388 ◽  
Author(s):  
Brian J. Del Buono ◽  
Patrick L. Williamson ◽  
Robert A. Schlegel
Keyword(s):  
Plasma Membrane ◽  
Membrane Lipid ◽  
Lymphocyte Differentiation ◽  
Plasma Membrane Lipid ◽  
Lipid Organization
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