Expression patterns of neuronal cell surface proteins plexin in developing mouse

1994 ◽  
Vol 19 ◽  
pp. S126
Author(s):  
Yasunori Murakami ◽  
Toshiki Kameyama ◽  
Atsushi Kawakami ◽  
Takashi Kitsukawa ◽  
Hajime Fujisawa
1999 ◽  
Vol 216 (1) ◽  
pp. 195-209 ◽  
Author(s):  
Beatrix P. Rubin ◽  
Richard P. Tucker ◽  
Doris Martin ◽  
Ruth Chiquet-Ehrismann

Neurology ◽  
2011 ◽  
Vol 77 (2) ◽  
pp. 179-189 ◽  
Author(s):  
E. Lancaster ◽  
E. Martinez-Hernandez ◽  
J. Dalmau

1994 ◽  
Vol 269 (16) ◽  
pp. 11987-11992 ◽  
Author(s):  
Y.A. Ushkaryov ◽  
Y. Hata ◽  
K. Ichtchenko ◽  
C. Moomaw ◽  
S. Afendis ◽  
...  

2019 ◽  
Author(s):  
Kaushiki P. Menon ◽  
Vivek Kulkarni ◽  
Shin-ya Takemura ◽  
Michael Anaya ◽  
Kai Zinn

ABSTRACTDrosophila R7 UV photoreceptors (PRs) are divided into yellow (y) and pale (p) subtypes with different wavelength sensitivities. yR7 PRs express the Dpr11 cell surface protein and are presynaptic to Dm8 amacrine neurons (yDm8) that express Dpr11’s binding partner DIP-γ, while pR7 PRs synapse onto DIP-γ-negative pDm8 neurons. Dpr11 and DIP-γ expression patterns define yellow and pale medulla color vision circuits that project to higher-order areas. DIP- γ and dpr11 mutations affect the morphology of yDm8 arbors in the yellow circuit. yDm8 neurons are generated in excess during development and compete for presynaptic yR7 partners. Transsynaptic interactions between Dpr11 and DIP-γ are required for generation of neurotrophic signals that allow yDm8 neurons to survive. yDm8 and pDm8 neurons do not normally compete for neurotrophic support, but can be forced to do so by manipulating R7 subtype fates. DIP-γ-Dpr11 interactions allow yDm8 neurons to select yR7 PRs as their home column partners.


Author(s):  
Watt W. Webb

Plasma membrane heterogeneity is implicit in the existence of specialized cell surface organelles which are necessary for cellular function; coated pits, post and pre-synaptic terminals, microvillae, caveolae, tight junctions, focal contacts and endothelial polarization are examples. The persistence of these discrete molecular aggregates depends on localized restraint of the constituent molecules within specific domaines in the cell surface by strong intermolecular bonds and/or anchorage to extended cytoskeleton. The observed plasticity of many of organelles and the dynamical modulation of domaines induced by cellular signaling evidence evanescent intermolecular interactions even in conspicuous aggregates. There is also strong evidence that universal restraints on the mobility of cell surface proteins persist virtually everywhere in cell surfaces, not only in the discrete organelles. Diffusion of cell surface proteins is slowed by several orders of magnitude relative to corresponding protein diffusion coefficients in isolated lipid membranes as has been determined by various ensemble average methods of measurement such as fluorescence photobleaching recovery(FPR).


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