Adult insect mushroom body neurons in primary culture: cell morphology and characterization of potassium channels

1998 ◽  
Vol 291 (3) ◽  
pp. 537-547 ◽  
Author(s):  
M. Cayre ◽  
S. D. Buckingham ◽  
A. Strambi ◽  
C. Strambi ◽  
D. B. Sattelle
2008 ◽  
Vol 44 (8-9) ◽  
pp. 309-320 ◽  
Author(s):  
Heribelt Tovar ◽  
Felipe Navarrete ◽  
Lleretny Rodríguez ◽  
Oscar Skewes ◽  
Fidel Ovidio Castro

1996 ◽  
Vol 17 (2) ◽  
pp. 165-169 ◽  
Author(s):  
HIROAKI YOSHIKAWA ◽  
YOSHIHIRO YASUKAWA ◽  
SOICHI OKINO ◽  
MASAHARU TAKAMORI ◽  
KATSUHIRA IIDA

Author(s):  
Jane K. Rosenthal ◽  
Dianne L. Atkins ◽  
William J. Marvin ◽  
Penny A. Krumm

To comprehend structural changes in cardiac myocytes accompanying adrenergic innervation, it is essential that a three dimensional analysis be performed. To date, biological studies which utilize stereological methods have been limited to cells in tissue and in organs. Our laboratory has utilized current stereological techniques for measuring absolute volumes of individual myocytes in primary culture. Cell volumes are calculated for two distinct groups of cells at 96 hours in culture: isolated myocytes and myocytes innervated with adrenergic neurons (Figure 1).Cardiac myocytes are cultured from the ventricular apices of newborn rats. Cells are plated directly onto tissue culture dishes with or without preplated explants from the paravertebral thoracolumbar sympathetic chain. On day four cultures are photographed and marked for one-to-one cell location. Following conventional fixation and embeddment in eponate-12, the cells are relocated and mounted for microtomy. The cells are completely sectioned at 120nm in their parallel orientation to the surface of the dish (Figure 2). Serial sections are collected on formvar coated slotted grids and are recorded in sequence.


1982 ◽  
Vol 47 (02) ◽  
pp. 128-131 ◽  
Author(s):  
F Esnard ◽  
E Dupuy ◽  
A M Dosne ◽  
E Bodevin

SummaryA preliminary characterization of a fibrinolytic inhibitor released by human umbilical vein endothelial cells in primary culture is reported. This molecule of Mr comprised between 2 × 105 and 106 and of μ2 mobility precipitates at 43% ammonium sulphate saturation and is totally adsorbed on Concanavalin A Sepharose 4 B. A possible relationship with a macroglobulins is discussed.


FEBS Letters ◽  
1990 ◽  
Vol 266 (1-2) ◽  
pp. 105-108 ◽  
Author(s):  
Manuel Kukuljan ◽  
Min Yi Li ◽  
Illani Atwater

2014 ◽  
Vol 4 ◽  
pp. 1-7 ◽  
Author(s):  
Hiroshi Kitani ◽  
Miyako Yoshioka ◽  
Takato Takenouchi ◽  
Mitsuru Sato ◽  
Noriko Yamanaka

2011 ◽  
Vol 43 (2) ◽  
pp. 83-90 ◽  
Author(s):  
G.F. Martins ◽  
B.A.M. Guedes ◽  
L.M. Silva ◽  
J.E. Serrão ◽  
C.L. Fortes-Dias ◽  
...  

1990 ◽  
Vol 11 ◽  
pp. S136
Author(s):  
Makoto Hamanoue ◽  
Kazuyuki Nakajima ◽  
Nobuyuki Takei ◽  
Shinichi Kohsaka
Keyword(s):  

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