Radioactive 33-P probes in hybridization to glass cDNA microarrays using neural tissues

2001 ◽  
Vol 106 (1) ◽  
pp. 9-13 ◽  
Author(s):  
Laurie Ward Whitney ◽  
Kevin G. Becker
Author(s):  
Juan Mora-Galindo ◽  
Jorge Arauz-Contreras

The zinc iodide-osmium tetroxide (ZIO) technique is presently employed to study both, neural and non neural tissues. Precipitates depends on cell types and possibly cell metabol ism as well.Guinea pig cecal mucosa, already known to be composed of epithelium with cells at different maturation stages and lamina propria which i s formed by morphologically and functionally heterogeneous cell population, was studied to determine the pat tern of ZIO impregnation. For this, adult Guinea pg cecal mucosa was fixed with buffered 1.2 5% g 1 utara 1 dehyde before incubation with ZIO for 16 hours, a t 4°C in the dark. Further steps involved a quick sample dehydration in graded ethanols, embedding in Epon 812 and sectioning to observe the unstained material under a phase contrast light microscope (LM) and a transmission electron microscope (TEM).


Author(s):  
Karolina Punovuori ◽  
Mattias Malaguti ◽  
Sally Lowell

AbstractDuring early neural development, changes in signalling inform the expression of transcription factors that in turn instruct changes in cell identity. At the same time, switches in adhesion molecule expression result in cellular rearrangements that define the morphology of the emerging neural tube. It is becoming increasingly clear that these two processes influence each other; adhesion molecules do not simply operate downstream of or in parallel with changes in cell identity but rather actively feed into cell fate decisions. Why are differentiation and adhesion so tightly linked? It is now over 60 years since Conrad Waddington noted the remarkable "Constancy of the Wild Type” (Waddington in Nature 183: 1654–1655, 1959) yet we still do not fully understand the mechanisms that make development so reproducible. Conversely, we do not understand why directed differentiation of cells in a dish is sometimes unpredictable and difficult to control. It has long been suggested that cells make decisions as 'local cooperatives' rather than as individuals (Gurdon in Nature 336: 772–774, 1988; Lander in Cell 144: 955–969, 2011). Given that the cadherin family of adhesion molecules can simultaneously influence morphogenesis and signalling, it is tempting to speculate that they may help coordinate cell fate decisions between neighbouring cells in the embryo to ensure fidelity of patterning, and that the uncoupling of these processes in a culture dish might underlie some of the problems with controlling cell fate decisions ex-vivo. Here we review the expression and function of cadherins during early neural development and discuss how and why they might modulate signalling and differentiation as neural tissues are formed.


2000 ◽  
Vol 21 ◽  
pp. 162
Author(s):  
Makoto Masumura ◽  
Ryuji Hata ◽  
Hiroyasu Akatsu ◽  
Takayuki Yamamoto ◽  
Hidechika Okada ◽  
...  

1999 ◽  
Vol 45 (4, Part 2 of 2) ◽  
pp. 157A-157A
Author(s):  
J Black ◽  
C Xiang ◽  
Y Chen ◽  
L Gillim ◽  
G Gooden ◽  
...  

2004 ◽  
Vol 32 (5) ◽  
pp. 476-482 ◽  
Author(s):  
Petra Håkansson ◽  
David Segal ◽  
Carin Lassen ◽  
Urban Gullberg ◽  
Herbert C Morse ◽  
...  
Keyword(s):  

Plant Science ◽  
2004 ◽  
Vol 167 (3) ◽  
pp. 457-469 ◽  
Author(s):  
Sandra Fonseca ◽  
László Hackler ◽  
Ágnes Zvara ◽  
Sı́lvia Ferreira ◽  
Aladje Baldé ◽  
...  

1962 ◽  
Vol 12 (2) ◽  
pp. 385-410 ◽  
Author(s):  
Sanford L. Palay ◽  
S. M. McGee-Russell ◽  
Spencer Gordon ◽  
Mary A. Grillo

This paper describes in detail a method for obtaining nearly uniform fixation of the nervous system by vascular perfusion with solutions of osmium tetroxide. Criteria are given for evaluating the degree of success achieved in the preservation of all the cellular components of the nervous system. The method permits analysis of the structural relations between cells at the electron microscopic level to an extent that has not been possible heretofore.


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