The Formation of Siliceous Scales by Raphidiophrys Ambigua (Protista, Centroheliozoa)

1988 ◽  
Vol 91 (1) ◽  
pp. 33-39
Author(s):  
DAVID J. PATTERSON ◽  
MONIKA DÜRRSCHMIDT

Ultrastructural aspects of the formation of siliceous scales by the protozoon Raphidiophrys ambigua are described. Cells in culture become scale-free in silicon-impoverished medium. Scales may be seen adhering to the cell surface within four to six hours of the addition of silicon to the medium. Silica scale formation occurs within deposition vesicles (SDVs) near the periphery of the cell. Many scales are formed at the same time; each may be in a different phase of scale formation. The source of the SDV membrane is not known. Silicification proceeds centrifugally from two pattern centres. The first parts of the forming scale are two opposed sterna, which establish the longitudinal axis of the scale. One sternum develops from each pattern centre. The scale develops outwards by formation of fairly evenly spaced lateral ribs from each central sternum. Distally, the ribs branch to form a reticulate pattern. A thin continuous sheet of silicon is added to the periphery of the scale, curving inwards to form a rim. The development of this pattern may be described in terms of a small number of morphogenetic processes.

1982 ◽  
Vol 92 (1) ◽  
pp. 231-236 ◽  
Author(s):  
J Prives ◽  
A B Fulton ◽  
S Penman ◽  
M P Daniels ◽  
C N Christian

To monitor the interaction of cell surface acetylcholine (AcCho) receptors with the cytoskeleton, cultured muscle cells were labeled with radioactive or fluorescent alpha-bungarotoxin and extracted with Triton X-100, using conditions that preserve internal structure. A significant population of the AcCho receptors is retained on the skeletal framework remaining after detergent extraction. The skeleton organization responsible for restricting AcCho receptors to a patched region may also result in their retention after detergent extraction.


1971 ◽  
Vol 78 (2) ◽  
pp. 171-176 ◽  
Author(s):  
G. Ågren ◽  
J. Pontén ◽  
G. Ronquist ◽  
B. Westermark

2016 ◽  
Vol 2 (1) ◽  
pp. 174-185 ◽  
Author(s):  
L. Lunevich ◽  
P. Sanciolo ◽  
A. Smallridge ◽  
S. R. Gray

Silica scale formation on reverse osmosis (RO) membrane surface is a significant problem for operation of high recovery RO desalination plant.


1981 ◽  
Vol 34 (1) ◽  
pp. 90-94 ◽  
Author(s):  
RUTH KOREN ◽  
HEDVA BERCOVITZ ◽  
HAMAO UMEZAWA ◽  
WERNER E. G. MÜLLER

1984 ◽  
Vol 217 (2) ◽  
pp. 377-381 ◽  
Author(s):  
N C Inestrosa

The present paper examines where the extracellular-matrix (ECM) 16S acetylcholinesterase (AChE, EC 3.1.1.7) is assembled in muscle cells in culture. The existence of an internal pool of 16S AChE was detected by using AChE inhibitors of differing membrane permeability. After irreversible inhibition of all cellular esterase, the newly synthesized 16S form appears in an intracellular compartment and is only later detected on the cell surface. Results show that the ECM 16S AChE is assembled within muscle cells.


1980 ◽  
Vol 44 (1) ◽  
pp. 187-200
Author(s):  
C.A. Erickson

Several aspects of the behaviour of polyoma virus-transformed BHK cells in culture have suggested that they are more deformable than BHK cells. This possibility was tested by applying negative pressure at the cell surface by means of a micropipette. It was found that PyBHK cells in early mitosis are twice as deformable as BHK cells in the same stage. In addition, the taut, non-ruffling margins of both cell types when fully spread are much less deformable than the extending, ruffling leading lamella. The degree of deformability of these cells is correlated with the distribution and organization of microfilaments and consistent with this, deformability increases greatly in the presence of cytochalasin B. The significance of deformability studies such as these is discussed.


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