Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/197421
Type: Artigo de periódico
Title: Inhibition Of Caspase-dependent Spontaneous Apoptosis Via A Camp-protein Kinase A Dependent Pathway In Neutrophils From Sickle Cell Disease Patients.
Author: Conran, Nicola
Almeida, Camila B
Lanaro, Carolina
Ferreira, Renata Proença
Traina, Fabiola
Saad, Sara T O
Costa, Fernando F
Abstract: Sickle cell disease (SCD) is a chronic inflammatory condition characterized by high leucocyte counts, altered cytokine levels and endothelial cell injury. As the removal of inflammatory cells by apoptosis is fundamental for the resolution of inflammation, we aimed to determine whether the leucocyte apoptotic process is altered in SCD. Neutrophils from SCD individuals showed an inhibition of spontaneous apoptosis when cultured in vitro, in the presence of autologous serum for 20 h. Intracellular cyclic adenosine monophosphate (cAMP) levels were approximately twofold increased in SCD neutrophils; possible cAMP-upregulating factors present in SCD serum include interleukin-8, granulocyte-macrophage colony-stimulating factor and prostaglandin. Accordingly, co-incubation of SCD neutrophils with KT5720, a cAMP-dependent protein kinase (PKA) inhibitor, abrogated increased SCD neutrophil survival. Caspase-3 activity was also significantly diminished in SCD neutrophils cultured for 16 h and this activity was restored when cells were co-incubated with KT5720. BIRC2 (encoding cellular inhibitor of apoptosis protein 1, cIAP(1)), MCL1 and BAX expression were unaltered in SCD neutrophils; however, BIRC3 (encoding the caspase inhibitor, cIAP(2)), was expressed at significantly higher levels. Thus, we report an inhibition of spontaneous SCD neutrophil apoptosis that appears to be mediated by upregulated cAMP-PKA signalling and decreased caspase activity. Increased neutrophil survival may have significant consequences in SCD; contributing to leucocytosis, tissue damage and exacerbation of the chronic inflammatory state.
Subject: Adult
Anemia, Sickle Cell
Annexin A5
Antisickling Agents
Apoptosis
Biological Markers
Carbazoles
Case-control Studies
Caspase 3
Cells, Cultured
Cyclic Amp
Cyclic Amp-dependent Protein Kinases
Female
Flow Cytometry
Gene Expression
Humans
Hydroxyurea
Indoles
Male
Neutrophils
Prostaglandins E
Pyrroles
Reverse Transcriptase Polymerase Chain Reaction
Up-regulation
Rights: fechado
Identifier DOI: 10.1111/j.1365-2141.2007.06748.x
Address: http://www.ncbi.nlm.nih.gov/pubmed/17711515
Date Issue: 2007
Appears in Collections:Unicamp - Artigos e Outros Documentos

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