Salicylate induced changes in outer hair cell lateral wall stiffness

1999 ◽  
Vol 135 (1-2) ◽  
pp. 163-168 ◽  
Author(s):  
Allen Jung-Chen Lue ◽  
William E Brownell
1998 ◽  
Vol 119 (1) ◽  
pp. 14-20 ◽  
Author(s):  
Thanh-Van N. Nguyen ◽  
William E. Brownell

The outer hair cell can be divided into three domains: the apex, the base, and the lateral wall. With the use of filipin, a polyene fluorescent antibiotic that binds to cholesterol, we found under fluorescence microscopy that the lateral wall membranes were less intensely stained than the apical and basal membranes. This difference in filipin fluorescence between the lateral walls and the ends diminished when cells were incubated in water-soluble cholesterol before staining, suggesting that exogenous cholesterol enters the lateral wall. Under confocal microscopy, we studied the incorporation pattern of a fluorescent cholesterol analogue, NBD-cholesterol. NBD-cholesterol did not stain the apical membranes whereas it intensely labeled the lateral wall. The micropipette aspiration technique was used to assess the effect of cholesterol on lateral wall stiffness. The lateral wall stiffness parameter of cells treated with water-soluble cholesterol ( n= 23) was significantly higher than that of controls ( n = 27): 0.76 ± 0.24 (mean ± SD) versus 0.46 ± 0.10 (Student's t test, p>0.001). In conclusion, cholesterol has different distributions among outer hair cell membranes, and when water-soluble cholesterol is incorporated into the cells, the outer hair cell lateral wall stiffness parameter increases. (Otolaryngol Head Neck Surg 1998;119:14–20.)


2008 ◽  
Vol 130 (3) ◽  
Author(s):  
Kristopher R. Schumacher ◽  
Aleksander S. Popel ◽  
Bahman Anvari ◽  
William E. Brownell ◽  
Alexander A. Spector

Cell membrane tethers are formed naturally (e.g., in leukocyte rolling) and experimentally to probe membrane properties. In cochlear outer hair cells, the plasma membrane is part of the trilayer lateral wall, where the membrane is attached to the cytoskeleton by a system of radial pillars. The mechanics of these cells is important to the sound amplification and frequency selectivity of the ear. We present a modeling study to simulate the membrane deflection, bending, and interaction with the cytoskeleton in the outer hair cell tether pulling experiment. In our analysis, three regions of the membrane are considered: the body of a cylindrical tether, the area where the membrane is attached and interacts with the cytoskeleton, and the transition region between the two. By using a computational method, we found the shape of the membrane in all three regions over a range of tether lengths and forces observed in experiments. We also analyze the effects of biophysical properties of the membrane, including the bending modulus and the forces of the membrane adhesion to the cytoskeleton. The model’s results provide a better understanding of the mechanics of tethers pulled from cell membranes.


1998 ◽  
Vol 18 (1) ◽  
pp. 48-58 ◽  
Author(s):  
John S. Oghalai ◽  
Alpen A. Patel ◽  
Takashi Nakagawa ◽  
William E. Brownell

2005 ◽  
Vol 33 (8) ◽  
pp. 991-1002 ◽  
Author(s):  
Alexander A. Spector ◽  
Aleksander S. Popel ◽  
Ruth Anne Eatock ◽  
William E. Brownell

2001 ◽  
Vol VI.01.1 (0) ◽  
pp. 181-182
Author(s):  
Hiroto USUKURA ◽  
Michiko SUGAWARA ◽  
Hiroshi WADA

1997 ◽  
Vol 117 (2) ◽  
pp. P91-P91
Author(s):  
J OGHALAI ◽  
T NAKAGAWA ◽  
A PATEL ◽  
W BROWNELL

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