Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2010-1-4
pubmed:abstractText
Cerebral ischemia-induced accumulation of unfolded proteins in vulnerable neurons triggers endoplasmic reticulum (ER) stress. Arginine-rich, mutated in early stage tumors (ARMET) is an ER stress-inducible protein and upregulated in the early stage of cerebral ischemia. The purposes of this study were to investigate the characteristics and implications of ARMET expression induced by focal cerebral ischemia. Focal cerebral ischemia in rats was induced by right middle cerebral artery occlusion with a suture; ischemic lesions were assessed by magnetic resonance imaging and histology; neuronal apoptosis was determined by TUNEL staining; the expressions of proteins were measured by immunohistochemistry, immunofluorescent labeling, and Western blotting. ARMET was found to be extensively upregulated in ischemic regions in a time-dependent manner. The expression of ARMET was neuronal in all examined structures in response to the ischemic insult. We also found that ARMET expression is earlier and more sensitive to ischemic stimulation than C/EBP homologous protein (CHOP). ER stress agent tunicamycin induced ARMET and CHOP expressions in the primary cultured neurons. Treatment with recombinant human ARMET promoted neuron proliferation and prevented from neuron apoptosis induced by tunicamycin. These results suggest that cerebral ischemia-induced ARMET expression may be protective to the neurons.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-10838596, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-11272179, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-11389192, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-11439185, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-11551913, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-11943137, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-12050113, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-12453408, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-12679722, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-12794311, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-14559994, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-1483388, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-15123740, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-15342372, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-15379881, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-1547942, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-15775988, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-16397584, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-16432136, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-17137721, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-17507765, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-17590517, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-17611540, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-18049481, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-18082969, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-18255062, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-18395193, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-18561914, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-18718866, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-18927462, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-19258449, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-19399876, http://linkedlifedata.com/resource/pubmed/commentcorrection/19773801-9531536
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1559-7016
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
30
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
79-91
pubmed:dateRevised
2011-7-20
pubmed:meshHeading
pubmed-meshheading:19773801-Animals, pubmed-meshheading:19773801-Blotting, Western, pubmed-meshheading:19773801-Brain Ischemia, pubmed-meshheading:19773801-Cells, Cultured, pubmed-meshheading:19773801-Coloring Agents, pubmed-meshheading:19773801-Endoplasmic Reticulum, pubmed-meshheading:19773801-Female, pubmed-meshheading:19773801-Fluorescent Antibody Technique, pubmed-meshheading:19773801-Immunohistochemistry, pubmed-meshheading:19773801-In Situ Nick-End Labeling, pubmed-meshheading:19773801-Infarction, Middle Cerebral Artery, pubmed-meshheading:19773801-Magnetic Resonance Imaging, pubmed-meshheading:19773801-Male, pubmed-meshheading:19773801-Nerve Growth Factors, pubmed-meshheading:19773801-Neurons, pubmed-meshheading:19773801-Pregnancy, pubmed-meshheading:19773801-Proteins, pubmed-meshheading:19773801-Rats, pubmed-meshheading:19773801-Rats, Sprague-Dawley, pubmed-meshheading:19773801-Tetrazolium Salts
pubmed:year
2010
pubmed:articleTitle
Induction profile of MANF/ARMET by cerebral ischemia and its implication for neuron protection.
pubmed:affiliation
Department of Radiology of the First Affiliated Hospital, Anhui Medical University, Hefei, China.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't