Document Detail


Immunohistochemical expression and colocalization of somatostatin, carboxypeptidase-E and prohormone convertases 1 and 2 in rat brain.
MedLine Citation:
PMID:  17543468     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The processing of many peptides for their maturation in target tissue depends upon the presence of sorting receptor. Several previous studies have predicted that carboxypeptidase-E (CPE), prohormone convertase 1 (PC1) and prohormone convertase 2 (PC2) may function as sorting elements for somatostatin (SST) for its maturation and processing to appropriate targets. However, nothing is currently known about whether brain, neuronal culture or even endocrine cells express SST, CPE, PC1 and PC2 and exhibit colocalization. Accordingly, in the present study using peroxidase immunohistochemistry, double-labeled indirect immunofluorescence immunohistochemistry and Western blot analysis, we mapped the distributional pattern of SST, CPE, PC1 and PC2 in different rat brain regions. Additionally, we also determined the colocalization of SST with CPE, PC1 and PC2 as well as colocalization of CPE with PC1 and PC2. The localization of SST, CPE, PC1 and PC2 reveals a distinct and region specific distribution pattern in the rat brain. Using an indirect double-label immunofluorescence method we observed selective neuron specific colocalization in a region specific manner in cortex, striatum and hippocampus. These studies provide the first evidence for colocalization between SST, CPE, PC1 and PC2 as well as CPE with PC1 and PC2. SST in cerebral cortex colocalized in pyramidal and non-pyramidal neurons with CPE, PC1 and PC2. Most importantly, in striatum and hippocampus colocalization was mostly observed selectively and preferentially in interneurons. CPE is also colocalized with PC1 and PC2 in a region specific manner. The data presented here provide a new insight into the distribution and colocalization of SST, CPE, PC1 and PC2 in rat brain. Taken together, our data anticipate the possibility that CPE, PC1 and PC2 might be potential target for the maturation of SST.
Authors:
S Billova; A S Galanopoulou; N G Seidah; X Qiu; U Kumar
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2007-06-01
Journal Detail:
Title:  Neuroscience     Volume:  147     ISSN:  0306-4522     ISO Abbreviation:  Neuroscience     Publication Date:  2007 Jun 
Date Detail:
Created Date:  2007-06-19     Completed Date:  2007-09-18     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7605074     Medline TA:  Neuroscience     Country:  United States    
Other Details:
Languages:  eng     Pagination:  403-18     Citation Subset:  IM    
Affiliation:
Faculty of Pharmaceutical Sciences, Department of Pharmacology and Toxicology, University of British Columbia, Vancouver, BC, Canada V6T 124.
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MeSH Terms
Descriptor/Qualifier:
Actins / metabolism
Animals
Blotting, Western
Brain / anatomy & histology
Brain Chemistry / physiology*
Carboxypeptidase H / metabolism*
Cerebral Cortex / enzymology,  metabolism
Fluorescent Antibody Technique, Indirect
Hippocampus / enzymology,  metabolism
Immunohistochemistry
Male
Neostriatum / enzymology,  metabolism
Proprotein Convertase 1 / metabolism*
Proprotein Convertase 2 / metabolism*
Rats
Rats, Sprague-Dawley
Somatostatin / metabolism*
Chemical
Reg. No./Substance:
0/Actins; 51110-01-1/Somatostatin; EC 3.4.17.10/Carboxypeptidase H; EC 3.4.21.93/Proprotein Convertase 1; EC 3.4.21.94/Proprotein Convertase 2

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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