Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2008-12-29
pubmed:abstractText
Corticotropin releasing factor receptor type 1 (CRF1), a coordinator of the body responses to stress, is also expressed in human skin, where it undergoes alternative splicing. Since the epidermis is continuously exposed to the environmental stress, human keratinocytes were chosen to study the biological role of CRF1 alternative splicing. The expression pattern of CRF1 isoforms depended on cell density, presence or absence of serum, and exposure to ultraviolet irradiation (UVR). Only two isoforms alpha and c were predominantly localized to the cell membrane, with only CRF1alpha being efficient in stimulating cAMP responding element (CRE). CRF1d, f and g had intracellular localization, showing no or very low (g) activation of CRE. The co-expression of CRF1alpha with d, f or g resulted in intracellular retention of both isoforms suggesting dimerization confirmed by detection of high molecular weight complexes. The soluble isoforms e and h were diffusely distributed in the cytoplasm or localized to the ER, respectively, and additionally found in culture medium. These findings suggest that alternatively spliced CRF1 isoforms can interact and modify CRF1alpha subcellular localization, thus affecting its activity. We suggest that alternative splicing of CRF1 may play an important role in the regulation of skin cell phenotype with potential implications in pathology.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-10598591, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-11606483, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-12196108, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-14605004, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-14684825, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-15206947, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-15701705, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-15749158, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-15944267, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-16245303, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-16393915, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-16484629, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-16720310, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-16888152, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-16956982, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-17175121, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-17318384, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-17330132, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-17400813, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-17536010, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-17620610, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-17878512, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-17913459, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-17959885, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-18199492, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-18362331, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-6267699, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-6273874, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-7589495, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-9506767, http://linkedlifedata.com/resource/pubmed/commentcorrection/19006179-9543169
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1097-4652
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
218
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
593-602
pubmed:dateRevised
2011-9-26
pubmed:meshHeading
pubmed-meshheading:19006179-Alternative Splicing, pubmed-meshheading:19006179-Cell Membrane, pubmed-meshheading:19006179-Cells, Cultured, pubmed-meshheading:19006179-Environment, pubmed-meshheading:19006179-Epidermis, pubmed-meshheading:19006179-Glycosylation, pubmed-meshheading:19006179-Humans, pubmed-meshheading:19006179-Keratinocytes, pubmed-meshheading:19006179-Luminescent Proteins, pubmed-meshheading:19006179-Models, Biological, pubmed-meshheading:19006179-Protein Binding, pubmed-meshheading:19006179-Protein Isoforms, pubmed-meshheading:19006179-Protein Transport, pubmed-meshheading:19006179-Receptors, Corticotropin-Releasing Hormone, pubmed-meshheading:19006179-Recombinant Fusion Proteins, pubmed-meshheading:19006179-Response Elements, pubmed-meshheading:19006179-Signal Transduction, pubmed-meshheading:19006179-Solubility, pubmed-meshheading:19006179-Subcellular Fractions, pubmed-meshheading:19006179-Ultraviolet Rays
pubmed:year
2009
pubmed:articleTitle
CRF1 receptor splicing in epidermal keratinocytes: potential biological role and environmental regulations.
pubmed:affiliation
Department of Pathology and Laboratory Medicine, Center for Cancer Research, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural