Source:http://linkedlifedata.com/resource/pubmed/id/18577698
Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
2008-9-8
|
| pubmed:abstractText |
The influence of sexual category as a modifier of cellular function is underinvestigated. Whether sex differences affect estrogen-mediated mitochondrial cytoprotection was determined using cell cultures of normal human lens epithelia (nHLE) from postmortem male and female donors. Experimental indicators assessed included differences in estrogen receptor-beta (ERbeta) isoform expression, receptor localization in mitochondria, and estrogen-mediated prevention of loss of mitochondrial membrane potential using the potentiometric fluorescent compound JC-1 after nHLE were exposed to peroxide. The impact of wild-type ERbeta (wtERbeta1) was also assessed using wtERbeta1 siRNA to suppress expression. A triple-primer PCR assay was employed to determine the proportional distribution of the receptor isoforms (wtERbeta1, -beta2, and -beta5) from the total ERbeta message pool in male and female cell cultures. Irrespective of sex, nHLE express wtERbeta1 and the ERbeta2 and ERbeta5 splice variants in similar ratios. Confocal microscopy and immunofluorescence revealed localization of the wild-type receptor in peripheral mitochondrial arrays and perinuclear mitochondria as well as nuclear staining in both cell populations. The ERbeta2 and ERbeta5 isoforms were distributed primarily in the nucleus and cytosol, respectively; no association with the mitochondria was detected. Both male and female nHLE treated with E(2) (1 muM) displayed similar levels of protection against peroxide-induced oxidative stress. In conjunction with acute oxidative insult, RNA suppression of wtERbeta1 elicited the collapse of mitochondrial membrane potential and markedly diminished the otherwise protective effects of E(2). Thus, whereas the estrogen-mediated prevention of mitochondrial membrane permeability transition is sex independent, the mechanism of estrogen-induced mitochondrial cytoprotection is wtERbeta1 dependent.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/5,5',6,6'-tetrachloro-1,1',3,3'-tetr...,
http://linkedlifedata.com/resource/pubmed/chemical/Benzimidazoles,
http://linkedlifedata.com/resource/pubmed/chemical/Carbocyanines,
http://linkedlifedata.com/resource/pubmed/chemical/Estrogen Receptor beta,
http://linkedlifedata.com/resource/pubmed/chemical/Fluorescent Dyes,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Small Interfering
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Sep
|
| pubmed:issn |
0193-1849
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
295
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
E637-47
|
| pubmed:meshHeading |
pubmed-meshheading:18577698-Benzimidazoles,
pubmed-meshheading:18577698-Blotting, Western,
pubmed-meshheading:18577698-Carbocyanines,
pubmed-meshheading:18577698-Cells, Cultured,
pubmed-meshheading:18577698-Cytoprotection,
pubmed-meshheading:18577698-Epithelial Cells,
pubmed-meshheading:18577698-Estrogen Receptor beta,
pubmed-meshheading:18577698-Female,
pubmed-meshheading:18577698-Fluorescent Dyes,
pubmed-meshheading:18577698-Humans,
pubmed-meshheading:18577698-Immunohistochemistry,
pubmed-meshheading:18577698-Lens, Crystalline,
pubmed-meshheading:18577698-Male,
pubmed-meshheading:18577698-Microscopy, Confocal,
pubmed-meshheading:18577698-Mitochondria,
pubmed-meshheading:18577698-Mitochondrial Membranes,
pubmed-meshheading:18577698-RNA, Small Interfering,
pubmed-meshheading:18577698-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:18577698-Sex Characteristics
|
| pubmed:year |
2008
|
| pubmed:articleTitle |
Role of wild-type estrogen receptor-beta in mitochondrial cytoprotection of cultured normal male and female human lens epithelial cells.
|
| pubmed:affiliation |
Department of Cell Biology, University of North Texas Health Science Center, Fort Worth, TX, USA.
|
| pubmed:publicationType |
Journal Article
|