Document Detail


Effect of thyroid hormone responsive protein (THRP) expression on PC12 cell survival.
MedLine Citation:
PMID:  12698219     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The thyroid hormone responsive protein (THRP) is a novel gene product that remains responsive to thyroid hormone in the cerebral cortex of adult rats. The biological effects of THRP are currently unknown. Since thyroid hormones (TH) are known to cause cell death in primary neuronal cultures, the effect of exogenous THRP expression on PC12 cell viability was investigated. Co-transfection of the THRP expression plasmid with the selectable marker pSV2neo resulted in a lower number of surviving PC12 cells compared to transfection with pSV2neo and the empty vector, pSVL. Similar results were observed when PC12 cells were transfected with the plasmid pCMV. SPORT beta-gal with and without pSVL-THRP. However, expression of exogenous THRP in the colonic epithelial cell line Caco-2 and the glial cell line U251 had no effect on cell viability. Coexpression of THRP with either the wild-type (WT)-c-Abl or a kinase-defective mutant c-Abl (K290R) did not alter the cell viability changes induced by THRP alone. Under these experimental conditions the predominant form of cell death was necrosis as evidenced by in situ analyses, such as terminal deoxynucleotidyl transferase (TdT)-mediated dUTP-biotin nick end labeling (TUNEL) and staining with membrane permeating and non-permeating nuclear dyes, Hoechst 33342 and propidium iodide respectively. In addition cell cycle arrest induced by THRP was demonstrated by reduced (3)H-thymidine incorporation into cellular DNA. The number of PC12 cells treated with 10(-7) M of l-3, 5, 3'-triiodothyronine (T(3)) was significantly reduced after the fourth day of culture. Treatment of the cells with T(3 )resulted in a dose dependent induction of THRP mRNA. It is concluded that: (1). THRP expression induces PC12 cell death; (2). under these experimental conditions the form of cell death is predominantly necrosis although cell cycle arrest may also occur; (3). the effect of THRP on cell viability is not modulated by c-Abl tyrosine kinase; and (4). the effect of T(3 )treatment on PC12 cell survival may be mediated by THRP.
Authors:
Michael J Haas; Shant A Parseghian; Raj M Sajid; Arshag D Mooradian
Related Documents :
12079679 - Pharmacological properties of rat alpha 7 nicotinic receptors expressed in native and r...
12056559 - Regulation of nociceptive neurons by nerve growth factor and glial cell line derived ne...
1646299 - Phospholipid-mediated delivery of anti-gap-43 antibodies into neuroblastoma cells preve...
8245509 - Agarose gel keratinocyte outgrowth system as a model of skin re-epithelization: require...
21984579 - Beta-cell uncoupling protein 2 regulates reactive oxygen species production, which infl...
17213629 - Real-time detection of dopamine released from a nerve model cell by an enzyme-catalyzed...
6050949 - Studies on the maintenance of oral development in tetrahymena pyriformis gl-c. ii. the ...
24794409 - Non-enzymatic oxygenated metabolites of α-linolenic acid b1- and l1-phytoprostanes prot...
10828539 - Anterograde axonal transport of glial cell line-derived neurotrophic factor and its rec...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2003-03-26
Journal Detail:
Title:  Experimental brain research     Volume:  150     ISSN:  0014-4819     ISO Abbreviation:  Exp Brain Res     Publication Date:  2003 May 
Date Detail:
Created Date:  2003-04-16     Completed Date:  2003-07-16     Revised Date:  2013-12-13    
Medline Journal Info:
Nlm Unique ID:  0043312     Medline TA:  Exp Brain Res     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  75-84     Citation Subset:  IM    
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Apoptosis / drug effects,  genetics
Cell Cycle / genetics
Cell Death / drug effects,  genetics*
Cell Survival / drug effects,  genetics*
DNA / biosynthesis
Genetic Vectors / diagnostic use
Homeodomain Proteins / genetics,  metabolism*
Necrosis
Neurons / drug effects,  metabolism*
PC12 Cells
Poly(ADP-ribose) Polymerases
Proteins / metabolism
Proto-Oncogene Proteins c-abl / deficiency,  genetics
RNA, Messenger / drug effects,  metabolism
Rats
Thyroxine / metabolism*
Transfection
Triiodothyronine / pharmacology
Chemical
Reg. No./Substance:
0/Abi2 protein, rat; 0/Homeodomain Proteins; 0/Proteins; 0/RNA, Messenger; 06LU7C9H1V/Triiodothyronine; 9007-49-2/DNA; EC 2.4.2.30/Adprt protein, rat; EC 2.4.2.30/Poly(ADP-ribose) Polymerases; EC 2.7.10.2/Proto-Oncogene Proteins c-abl; Q51BO43MG4/Thyroxine

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


Previous Document:  Effects of ethanol on anti-saccade task performance.
Next Document:  Kinaesthetic neurons in thalamus of humans with and without tremor.