Neural cell adhesion molecules influence second messenger systems
U. Schuch, M. Lohse, and M. Schachner. Neuron, 3 (1):
13-20(July 1989)Schuch, U Lohse, M J Schachner, M Research Support, Non-U.S. Gov't
United states Neuron Neuron. 1989 Jul;3(1):13-20..
Abstract
We have investigated the influence of the neural cell adhesion molecules
L1 and N-CAM on second messenger systems using a PC12 rat pheochromocytoma
cell line as a model and triggering cell surface receptors by specific
antibody binding. Antibodies directed against L1 and N-CAM, but not
against other cell surface components, reduce intracellular levels
of the inositol phosphates IP2 and IP3, while intracellular levels
of cAMP are unaffected. Antibodies against L1 and N-CAM also reduce
intracellular pH and increase intracellular Ca2+ by opening Ca2+
channels in a pertussis toxin-inhibitable manner, suggesting the
involvement of a G protein in the signal transduction process. Cross-linking
of the adhesion molecules on the surface membrane is not required
for the effects to occur. Furthermore, adhesion of single PC12 cells
to each other elicits effects on intracellular pH and Ca2+ similar
to those seen after application, underscoring the physiological significance
of the observed changes.
%0 Journal Article
%1 Schuch1989
%A Schuch, U.
%A Lohse, M. J.
%A Schachner, M.
%D 1989
%J Neuron
%K AMP/*metabolism Adhesion Animals Antibodies Bordetella/pharmacology Calcium Calcium/*metabolism Cell Channels/metabolism Concentration Cultured Cyclic Fab Factors, Fragments Hydrogen-Ion Immunoglobulin Inositol Messenger Molecules, Neuronal/immunology/*physiology Pertussis Phosphates/*metabolism Rats Second Signal Systems/*physiology Toxin Transduction Tumor Virulence
%N 1
%P 13-20
%T Neural cell adhesion molecules influence second messenger systems
%U http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=2559759
%V 3
%X We have investigated the influence of the neural cell adhesion molecules
L1 and N-CAM on second messenger systems using a PC12 rat pheochromocytoma
cell line as a model and triggering cell surface receptors by specific
antibody binding. Antibodies directed against L1 and N-CAM, but not
against other cell surface components, reduce intracellular levels
of the inositol phosphates IP2 and IP3, while intracellular levels
of cAMP are unaffected. Antibodies against L1 and N-CAM also reduce
intracellular pH and increase intracellular Ca2+ by opening Ca2+
channels in a pertussis toxin-inhibitable manner, suggesting the
involvement of a G protein in the signal transduction process. Cross-linking
of the adhesion molecules on the surface membrane is not required
for the effects to occur. Furthermore, adhesion of single PC12 cells
to each other elicits effects on intracellular pH and Ca2+ similar
to those seen after application, underscoring the physiological significance
of the observed changes.
@article{Schuch1989,
abstract = {We have investigated the influence of the neural cell adhesion molecules
L1 and N-CAM on second messenger systems using a PC12 rat pheochromocytoma
cell line as a model and triggering cell surface receptors by specific
antibody binding. Antibodies directed against L1 and N-CAM, but not
against other cell surface components, reduce intracellular levels
of the inositol phosphates IP2 and IP3, while intracellular levels
of cAMP are unaffected. Antibodies against L1 and N-CAM also reduce
intracellular pH and increase intracellular Ca2+ by opening Ca2+
channels in a pertussis toxin-inhibitable manner, suggesting the
involvement of a G protein in the signal transduction process. Cross-linking
of the adhesion molecules on the surface membrane is not required
for the effects to occur. Furthermore, adhesion of single PC12 cells
to each other elicits effects on intracellular pH and Ca2+ similar
to those seen after application, underscoring the physiological significance
of the observed changes.},
added-at = {2010-12-14T18:12:02.000+0100},
author = {Schuch, U. and Lohse, M. J. and Schachner, M.},
biburl = {https://www.bibsonomy.org/bibtex/2cb68d3b8bd545d2151b1b34b4eaf8b8d/pharmawuerz},
endnotereftype = {Journal Article},
interhash = {25d85a819584c50333db544c53d234e3},
intrahash = {cb68d3b8bd545d2151b1b34b4eaf8b8d},
issn = {0896-6273 (Print) 0896-6273 (Linking)},
journal = {Neuron},
keywords = {AMP/*metabolism Adhesion Animals Antibodies Bordetella/pharmacology Calcium Calcium/*metabolism Cell Channels/metabolism Concentration Cultured Cyclic Fab Factors, Fragments Hydrogen-Ion Immunoglobulin Inositol Messenger Molecules, Neuronal/immunology/*physiology Pertussis Phosphates/*metabolism Rats Second Signal Systems/*physiology Toxin Transduction Tumor Virulence},
month = Jul,
note = {Schuch, U Lohse, M J Schachner, M Research Support, Non-U.S. Gov't
United states Neuron Neuron. 1989 Jul;3(1):13-20.},
number = 1,
pages = {13-20},
shorttitle = {Neural cell adhesion molecules influence second messenger systems},
timestamp = {2010-12-14T18:20:50.000+0100},
title = {Neural cell adhesion molecules influence second messenger systems},
url = {http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=2559759},
volume = 3,
year = 1989
}