Cloning of the glucocorticoid receptor (GR) in gilthead seabream (Sparus aurata). Differential expression of GR and immune genes in gilthead seabream after an immune challenge. | - CCMAR -

Journal Article

TítuloCloning of the glucocorticoid receptor (GR) in gilthead seabream (Sparus aurata). Differential expression of GR and immune genes in gilthead seabream after an immune challenge.
Publication TypeJournal Article
AuthorsAcerete, L, Balasch, JC, Castellana, B, Redruello, B, Roher, N, Canario, AVM, Planas, JV, MacKenzie, S, Tort, L
Year of Publication2007
JournalComp Biochem Physiol B Biochem Mol Biol
Volume148
Questão1
Date Published2007 Sep
Pagination32-43
ISSN1096-4959
Palavras-chaveAmino Acid Sequence, Animals, Base Sequence, Cloning, Molecular, Gene Expression, Gene Expression Profiling, Hydrocortisone, Inflammation Mediators, Lipopolysaccharides, Molecular Sequence Data, Phylogeny, Receptors, Glucocorticoid, Reverse Transcriptase Polymerase Chain Reaction, Sea Bream
Abstract

In order to determine the cortisol response after an immune challenge in the gilthead seabream (Sparus aurata), a cortisol receptor (GR) was cloned, sequenced and its expression determined after lipopolysaccharide (LPS) treatment. To clone the gilthead seabream GR (sbGR), consecutive PCR amplifications and screening of a pituitary cDNA library were performed. We obtained a clone of 4586 bp encoding a 784aa protein. Northern blot analysis from head kidney, heart and intestine revealed that the full length sbGR mRNA was approximately 6.5 Kb. A LPS treatment, used as an acute stress model, was employed to characterise the expression of sbGR and some selected genes involved in the immune response (IL-1beta, TNF-alpha, Mx protein, cathepsin D and PPAR-gamma). All genes were expressed in all tissues examined and responses were tissue and time dependent revealing differential gene expression profiles after LPS administration. Furthermore, analysis of plasma cortisol levels after LPS injection, showed an acute response to inflammatory stress with a significant increase two and six h after injection, recovering to basal levels 12 h post-stress in all LPS concentrations tested.

DOI10.1016/j.cbpb.2007.04.015
Sapientia

http://www.ncbi.nlm.nih.gov/pubmed/17544309?dopt=Abstract

Alternate JournalComp. Biochem. Physiol. B, Biochem. Mol. Biol.
PubMed ID17544309
CCMAR Authors