The erythrocyte plasma membrane in murine muscular dystrophy: a scanning electron microscopic and freeze fracture study

1979 ◽  
Vol 57 (5) ◽  
pp. 983-986 ◽  
Author(s):  
Burr G. Atkinson ◽  
Richard R. Shivers ◽  
Bruce Nixon ◽  
Kristine H. Atkinson
Keyword(s):  
Plasma Membrane ◽  
Muscular Dystrophy ◽  
Red Blood Cells ◽  
Blood Cells ◽  
Plasma Membranes ◽  
Genetic Disorder ◽  
Freeze Fracture ◽  
Congenital Muscular Dystrophy ◽  
Molecular Architecture ◽  
Intramembrane Particles

The plasma membrane of red blood cells from mice afflicated with congenital muscular dystrophy exhibits a dramatic depletion of intramembrane particles. Examination of protein particles on fracture faces of erythrocyte plasma membranes from dystrophic mice revealed a 33% decrease in the number of intramembrane particles when compared with similarly prepared erythrocytes from nondystrophic animals. This alteration in the internal molecular architecture of these plasma membranes is correlated with the morphological distortion manifested by most red blood cells from mice inflicted with this genetic disorder.

Topology of morphologically detectable protein and cholesterol in membranes of polypeptide-secreting cells

1981 ◽  
Vol 296 (1080) ◽  
pp. 47-54 ◽  
Keyword(s):  
Plasma Membrane ◽  
Secretory Granule ◽  
Plasma Membranes ◽  
Secretory Pathway ◽  
Freeze Fracture ◽  
Fracture Morphology ◽  
Cholesterol Content ◽  
Intramembrane Particles ◽  
Exocrine Cells ◽  
Luminal Membrane

The freeze-fracture morphology of intracellular and plasma membranes in endocrine and exocrine polypeptide-secreting cells has been studied to detect changes while these membranes interact during secretion. A qualitative and quantitative evaluation of intramembrane particles and filipin binding as indicators of protein and cholesterol content of the membranes, respectively, reveals the following changes. From the forming of the maturing pole of the Golgi complex, membranes lose morphologically detectable protein and gain morphologically detectable cholesterol. The protein-poor, cholesterol-rich secretory granule membrane then interacts with a richly particulate plasma membrane in endocrine cells and with a moderately particulate luminal membrane in exocrine cells. The site of interaction between secretory granule and plasma membrane is characterized by a local clearing of intramembrane particles; by contrast, filipin-binding sites revealing cholesterol are present in this area. In exocrine cells, the fused secretory granule, which is initially rich in filipin-cholesterol complexes and poor in particles, appears to lose progressively its filipin labelling to resemble the poorly labelled luminal membrane. These findings, although they cannot be interpreted definitely at present, clearly show impressive changes of membrane structure along the secretory pathway and suggest that a corresponding degree of functional specialization is needed for proper interaction to occur.

Volatile Anesthetics Selectively Inhibit the Calcium sup 2+ -transporting ATPase in Neuronal and Erythrocyte Plasma Membranes

1996 ◽  
Vol 84 (5) ◽  
pp. 1189-1195 ◽  
Author(s):  
Ioulia Fomitcheva ◽  
Danuta Kosk-Kosicka
Keyword(s):  
Plasma Membrane ◽  
Red Blood Cells ◽  
Blood Cells ◽  
Plasma Membranes ◽  
Minimum Alveolar Concentration ◽  
Volatile Anesthetics ◽  
Sodium Pentobarbital ◽  
Synaptosomal Membranes ◽  
General Anesthetics ◽  
Neuronal Membranes

Background The activity of the plasma membrane Ca(2+)-transporting adenosine triphosphatase (PMCA) is inhibited by volatile anesthetics at clinical concentrations. The goal of the current study was to determine whether the inhibition is selective as compared to other adenosine triphosphatases (ATPases) and another group of general anesthetics, barbiturates. In addition, the authors determined whether the response to anesthetics of the enzymes in neuronal membranes is similar to that in erythrocyte membranes. Methods The effects of halothane, isoflurane, and sodium pentobarbital on four different ATPase activities were studied at 37 degrees C in two distinct plasma membrane preparations, human red blood cells and synaptosomal membranes from rat cerebellum. Results Inhibition patterns of the PMCA by halothane and isoflurane at anesthetic concentrations were vary similar in red blood cells and synaptosomal membranes. The half-maximal inhibition (I50) occurred at 0.25-0.30 mM halothane and 0.30-0.32 mM isoflurane. The PMCA in both membranes was significantly more sensitive to the inhibitory action of volatile anesthetics (I50 = 0.75-1.15 minimum alveolar concentration) than were other ATPases, such as the Na+,K+-ATPase (I50 approximately 3 minimum alveolar concentration) or Mg(2+)-ATPase (I50 > or = 5 minimum alveolar concentration). In contrast, sodium pentobarbital inhibited the PMCA in both membranes only at approximately 100-200-fold above its anesthetic concentrations. The other ATPases were inhibited at similar pentobarbital concentrations (I50 = 11-22 mM). Conclusions The findings demonstrate analogous response of the PMCA of neuronal and erythrocyte cells to two groups of general anesthetics. The PMCA activity is selectively inhibited by volatile anesthetics at their clinical concentrations. The enzyme in vivo may then be a pharmacologic target for volatile anesthetics but not for barbiturates.

Heterogeneity of Size and Distribution of Intramembrane Particles in the Plasma Membrane of Yeast

1977 ◽  
Vol 35 ◽  
pp. 596-597
Author(s):  
E. Keyhani
Keyword(s):  
Plasma Membrane ◽  
Candida Utilis ◽  
Synthetic Medium ◽  
Freeze Fracture ◽  
Translational Diffusion ◽  
Yeast Cells ◽  
Distilled Water ◽  
Intramembrane Particles ◽  
The Matrix ◽  
Water Cell

The matrix of biological membranes consists of a lipid bilayer into which proteins or protein aggregates are intercalated. Freeze-fracture techni- ques permit these proteins, perhaps in association with lipids, to be visualized in the hydrophobic regions of the membrane. Thus, numerous intramembrane particles (IMP) have been found on the fracture faces of membranes from a wide variety of cells (1-3). A recognized property of IMP is their tendency to form aggregates in response to changes in experi- mental conditions (4,5), perhaps as a result of translational diffusion through the viscous plane of the membrane. The purpose of this communica- tion is to describe the distribution and size of IMP in the plasma membrane of yeast (Candida utilis).Yeast cells (ATCC 8205) were grown in synthetic medium (6), and then harvested after 16 hours of culture, and washed twice in distilled water. Cell pellets were suspended in growth medium supplemented with 30% glycerol and incubated for 30 minutes at 0°C, centrifuged, and prepared for freeze-fracture, as described earlier (2,3).

scholarly journals The plasma membrane Ca2+-ATPase protein from red blood cells is not modified in preeclampsia

2006 ◽  
Vol 1762 (3) ◽  
pp. 381-385 ◽  
Author(s):  
Néstor J. Oviedo ◽  
Gustavo Benaim ◽  
Vincenza Cervino ◽  
Teresa Proverbio ◽  
Fulgencio Proverbio ◽  
...  
Keyword(s):  
Plasma Membrane ◽  
Red Blood Cells ◽  
Blood Cells

scholarly journals Isolation and properties of glycophorin from plasma membrane of hen red blood cells

1996 ◽  
Vol 12 (4) ◽  
pp. 94-99 ◽  
Author(s):  
T. V. Stasyk ◽  
M. D. Lutsik-Kordovsky
Keyword(s):  
Plasma Membrane ◽  
Red Blood Cells ◽  
Blood Cells

Freeze–fracture analysis of muscle plasma membrane in Becker's muscular dystrophy

1994 ◽  
Vol 20 (5) ◽  
pp. 487-494 ◽  
Author(s):  
S. Shibuya ◽  
Y. Wakayama ◽  
T. Jimi ◽  
H. Oniki ◽  
T. Kobayashi ◽  
...  
Keyword(s):  
Plasma Membrane ◽  
Muscular Dystrophy ◽  
Freeze Fracture ◽  
Fracture Analysis ◽  
Muscle Plasma Membrane

scholarly journals Surface membrane vesicles from mononuclear cells stimulate erythroid stem cells to proliferate in culture

Blood ◽  
1982 ◽  
Vol 60 (3) ◽  
pp. 583-594 ◽  
Author(s):  
N Dainiak ◽  
CM Cohen
Keyword(s):  
Plasma Membrane ◽  
Plasma Membranes ◽  
Mononuclear Cells ◽  
Surface Membrane ◽  
Freeze Fracture ◽  
Membrane Vesicles ◽  
Cell Types ◽  
Target Cells ◽  
Freeze Fracture Electron Microscopy

Abstract In order to examine the contribution of cell surface materials to erythroid burst-promoting activity (BPA), we separated media conditioned by a variety of human cell types into pellets and supernatants by centrifugation. When added to serum-restricted cultures of nonadherent human marrow cells, pellets contained about half of the total stimulatory activity. Freeze-fracture electron microscopy of the pellets revealed the presence of unilamellar membrane vesicles ranging from 0.10 to 0.40 microM in diameter. The amount of BPA in culture increased with added vesicle concentration in a saturable fashion. Preparation of leukocyte conditioned medium (LCM) from 125I-wheat germ agglutinin labeled cells and studies comparing the glycoprotein composition of vesicles with that of leukocyte plasma membranes suggest that LCM-derived vesicles are of plasma membrane origin. Moreover, partially purified leukocyte plasma membrane preparations also contained BPA. While disruption of vesicles by freezing/thawing and hypotonic lysis did not alter BPA, heat, trypsin, or pronase treatment removed greater than 65% of BPA, implying that vesicle surface rather than intravesicular molecules express BPA. Results of BPA assays performed in two-layer clots indicated that proximity to target cells is required for vesicle BPA expression. We conclude that membrane vesicles spontaneously shed from cell surfaces may be important regulators of erythroid burst proliferation in vitro.

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