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1.
Int J Cardiol ; 168(4): 3909-12, 2013 Oct 09.
Artigo em Inglês | MEDLINE | ID: mdl-23871616

RESUMO

BACKGROUND: Higher levels of C-reactive protein (CRP) predict cardiovascular events and also portend a poorer prognosis in patients with acute coronary syndromes. Much in-vitro and in-vivo data support a role for CRP in atherogenesis. METHODS: Using the one-bead-one-compound (OBOC) combinatorial library method we have successfully identified peptides against human CRP that inhibit its biological effects in-vitro. Hence we tested the effect of the best characterized inhibitor (CRP-i2) on the effects of CRP in an appropriate animal model, Wistar rats. RESULTS: Treatment with CRP resulted in significant increase in superoxide anion, nuclear factor kappaB (NFκb) activity and the release of biomarkers of inflammation from macrophages compared to Wistar rats treated with human albumin (HuSA). Pre-treatment with the inhibitor, CRP-i2, resulted in a significant reduction in CRP induced superoxide anion, NFκb activity and biomarkers of inflammation. Also, there were no observed clinical or laboratory related adverse effects. CONCLUSIONS: We demonstrate that our novel peptide inhibitor attenuates the proinflammatory effects of CRP in-vivo. Future studies will examine the long-term effects of this inhibitor on vascular pathobiology.


Assuntos
Proteína C-Reativa/antagonistas & inibidores , Proteína C-Reativa/metabolismo , Mediadores da Inflamação/antagonistas & inibidores , Mediadores da Inflamação/sangue , Inflamação/sangue , Fragmentos de Peptídeos/farmacologia , Animais , Proteína C-Reativa/toxicidade , Humanos , Inflamação/prevenção & controle , Fragmentos de Peptídeos/uso terapêutico , Ratos , Ratos Wistar
2.
J Immunol ; 167(11): 6210-6, 2001 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-11714782

RESUMO

2B4 (CD244), a member of the CD2 subset of the Ig superfamily receptors, is expressed on all human NK cells, a subpopulation of T cells, basophils and monocytes. 2B4 activates NK cell mediated cytotoxicity, induces secretion of IFN-gamma and matrix metalloproteinases, and NK cell invasiveness. Although there have been several molecules shown to interact with 2B4, the signaling mechanism of 2B4-mediated activation of NK cells is still unknown. In this study, we found cross-linking of 2B4 on YT cells, a human NK cell line, results in the increased DNA binding activity of activator protein-1 (AP-1), an important regulator of nuclear gene expression in leukocytes. We investigated the possible role of various signaling molecules that may be involved in the activation of lytic function of YT cells via 2B4. Treatment of YT cells with various specific inhibitors indicate that 2B4-stimulation of YT cells in spontaneous and Ab-dependent cytotoxicity is Ras/Raf dependent and involves multiple MAPK signaling pathways (ERK1/2 and p38). However, only inhibitors of transcription and p38 inhibited 2B4-mediated IFN-gamma release indicating distinct pathways are involved in cytotoxicity and cytokine release. In this study we also show that 2B4 constitutively associates with the linker for activation of T cells (LAT) and that 2B4 may mediate NK cell activation via a LAT-dependent signaling pathway. These results indicate that 2B4-mediated activation of NK cells involves complex interactions involving LAT, Ras, Raf, ERK and p38 and that cytolytic function and cytokine production may be regulated by distinct pathways.


Assuntos
Proteínas Adaptadoras de Transdução de Sinal , Antígenos CD , Citotoxicidade Imunológica/imunologia , Interferon gama/metabolismo , Células Matadoras Naturais/imunologia , Ativação Linfocitária/imunologia , Glicoproteínas de Membrana/fisiologia , Proteínas de Membrana , Receptores Imunológicos , Transdução de Sinais/imunologia , Animais , Proteínas de Transporte/metabolismo , Humanos , Células K562 , Células Matadoras Naturais/enzimologia , Células Matadoras Naturais/metabolismo , MAP Quinase Quinase 1 , Glicoproteínas de Membrana/metabolismo , Camundongos , Quinases de Proteína Quinase Ativadas por Mitógeno/fisiologia , Proteínas Quinases Ativadas por Mitógeno/fisiologia , Fosfoproteínas/metabolismo , Proteínas Serina-Treonina Quinases/fisiologia , Família de Moléculas de Sinalização da Ativação Linfocitária , Fator de Transcrição AP-1/metabolismo , Transcrição Gênica/imunologia , Células Tumorais Cultivadas , Proteínas Quinases p38 Ativadas por Mitógeno , Proteínas ras/fisiologia
3.
J Immunol ; 166(10): 6188-95, 2001 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-11342640

RESUMO

The cell surface glycoprotein 2B4 (CD244) of the Ig superfamily is involved in the regulation of NK and T lymphocyte functions. We have recently identified CD48 as the high affinity counterreceptor for 2B4 in both mice and humans. The cytoplasmic domain of 2B4 associates with src homology 2 domain-containing protein or signaling lymphocyte activation molecule-associated protein, whose mutation is the underlying genetic defect in the X-linked lymphoproliferative syndrome. In this study, we report the molecular cloning and characterization of the human 2B4 (h2B4) promoter. Through primer extension analysis, we found that the transcription of the h2B4 gene initiates at multiple start sites. We isolated h2B4 genomic clones and PCR amplified the 5' untranslated region containing the promoter elements. We have identified a functional AP-1 site that lies between (-106 to -100) through transient transfection analysis in YT cells, a human NK cell line. EMSAs with Abs specific for various protein factors of the AP-1 family revealed that multiple members of the Jun family are involved in the regulation of the h2B4 gene. Mutation of the AP-1 site not only abolishes protein/DNA interactions but also promoter activity. These results demonstrate a significant role for AP-1 in the transcriptional regulation of the h2B4 gene.


Assuntos
Antígenos CD , Células Matadoras Naturais/metabolismo , Glicoproteínas de Membrana/genética , Glicoproteínas de Membrana/metabolismo , Receptores Imunológicos , Fator de Transcrição AP-1/fisiologia , Transcrição Gênica/imunologia , Regiões 5' não Traduzidas/isolamento & purificação , Sequência de Bases , Sítios de Ligação/genética , Sítios de Ligação/imunologia , Proteínas de Ligação a DNA/genética , Proteínas de Ligação a DNA/metabolismo , Proteínas de Ligação a DNA/fisiologia , Eletroforese em Gel de Poliacrilamida , Regulação da Expressão Gênica/imunologia , Humanos , Células K562 , Células Matadoras Naturais/imunologia , Glicoproteínas de Membrana/biossíntese , Dados de Sequência Molecular , Regiões Promotoras Genéticas/imunologia , RNA Mensageiro/biossíntese , Família de Moléculas de Sinalização da Ativação Linfocitária , Fator de Transcrição AP-1/genética , Fator de Transcrição AP-1/metabolismo , Células Tumorais Cultivadas
6.
Immunogenetics ; 51(4-5): 306-13, 2000 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-10803843

RESUMO

Natural killer (NK)-cell recognition of target cells and cytolytic function are controlled by multiple receptor-ligand interactions. These receptors can transmit either positive or negative signals and belong to the lectin superfamily or immunoglobulin superfamily (IgSF). One member of the IgSF, 2B4, is expressed on the surface of all mouse and human NK cells and the subset of T cells that mediate NK-like killing. In both mouse and human, 2B4 is a transmembrane protein and is the counter-receptor for CD48. Northern blot analysis had indicated the existence of 2B4-related genes. Here we report the cloning of novel cDNAs (r2B4R) closely related to the rat 2B4. Unlike 2B4, rat NK cells express mRNA corresponding to both transmembrane (r2B4R-tm) and soluble (r2B4R-se) forms of r2B4R. r2B4R-tm contains an open reading frame encoding a polypeptide of 311 amino acid residues. The encoded protein has characteristics of type I transmembrane proteins with a 20-amino acid leader sequence, a 203-amino acid extracellular domain, a 23-amino acid transmembrane domain, and a 65-amino acid cytoplasmic domain. r2B4R-se encodes a protein of 205 amino acid residues without a putative transmembrane domain. Northern blot analysis and reverse transcriptase-PCR analysis revealed that both transmembrane and soluble forms of r2B4R are expressed in interleukin-2-activated NK cells.


Assuntos
Antígenos CD , Células Matadoras Naturais/imunologia , Proteínas de Membrana/genética , Receptores Imunológicos , Sequência de Aminoácidos , Animais , Sequência de Bases , DNA Complementar , Glicoproteínas de Membrana/genética , Proteínas de Membrana/metabolismo , Dados de Sequência Molecular , Ratos , Homologia de Sequência de Aminoácidos , Família de Moléculas de Sinalização da Ativação Linfocitária , Solubilidade
7.
Mol Immunol ; 37(12-13): 735-44, 2000.
Artigo em Inglês | MEDLINE | ID: mdl-11275258

RESUMO

2B4 (CD244) is a cell surface glycoprotein of the immunoglobulin superfamily involved in the regulation of natural killer and T lymphocyte function. It is the high affinity counter-receptor for CD48. In mouse and human NK cells, crosslinking of 2B4 with a specific monoclonal antibody or with CD48 can trigger cell-mediated cytotoxicity, IFN-gamma secretion, phosphoinositol turnover and NK cell invasiveness. Recent reports of defective 2B4 signaling and NK cell function in X-linked lymphoproliferative syndrome suggest that this may contribute to the progression of this human disease. Here we describe the molecular characterization of the rat 2B4 gene. The cDNA encodes a protein of 395 amino acid residues that contain two Ig domains in the extracellular region and three unique tyrosine motifs (TxYxxV/I/A) in the cytoplasmic region. The predicted protein has 81 and 68% similarity with mouse 2B4 and human 2B4, respectively. Additionally, it has 94 and 89% similarity at the protein level with the recently reported rat 2B4 related genes, r2B4R-tm and r2B4R-se respectively. Northern blot analysis indicated the presence of multiple transcripts in rat LAK cells and RNK-16 cells. Immunoprecipitation and deglycosylation studies showed that rat 2B4 is glycosylated to similar extent as that of mouse and human 2B4. The cloning of r2B4 in the light of the availability of rat NK cell lines should facilitate in vitro and in vivo experiments to decipher the functional role of 2B4 in NK cell biology.


Assuntos
Antígenos CD , Células Matadoras Naturais/imunologia , Glicoproteínas de Membrana/genética , Receptores Imunológicos/genética , Sequência de Aminoácidos , Animais , Sequência de Bases , Biblioteca Gênica , Glicoproteínas de Membrana/imunologia , Dados de Sequência Molecular , RNA Mensageiro/genética , Ratos , Receptores Imunológicos/imunologia , Análise de Sequência de DNA , Homologia de Sequência de Aminoácidos , Família de Moléculas de Sinalização da Ativação Linfocitária , Especificidade da Espécie
8.
Biochim Biophys Acta ; 1447(2-3): 244-50, 1999 Oct 28.
Artigo em Inglês | MEDLINE | ID: mdl-10542322

RESUMO

Natural killer (NK) cells are bone marrow-derived lymphocytes that have the ability to kill certain tumor cells and virally infected cells. The activation of NK cells is mediated by a balance of negative and positive signals from cell-cell interactions and from responses to cytokines. However, the molecular basis of NK cell activation and recognition of target cells is poorly understood. We have previously identified, cloned and characterized a receptor, 2B4, expressed on murine NK cells. 2B4 is not only expressed on all NK cells, but also on a subset of T-cells which have NK-like killing properties. Structural analysis indicated that 2B4 belongs to the CD2 subset of immunoglobulin superfamily. We have also shown 2B4 to interact with CD48 with nine times more affinity than that of CD2-CD48 interaction. In order to understand the transcriptional regulation as well as the mechanisms controlling the restricted expression of the 2B4 gene, we obtained a genomic 2B4 clone including the sequence of the 5'-flanking region. To define the start site of transcription, we performed primer extension and 5'-RACE assays and found that the 2B4 gene may be initiated at multiple start sites and driven by a TATA-less promoter. Transient transfections of nested 5'-fragments of the 2B4 promoter to drive CAT expression revealed tissue specific expression in CTLL-2 cells, a mouse T-cell line. A promoter fragment of 348 bases upstream from the first base of the mouse 2B4 cDNA clone p2B4.8 produced maximal CAT activity in CTLL-2 cells. The presence of the region -653 to -540 on the other hand, drastically reduced transcription. Sequence analysis of this promoter region has identified potential recognition motifs for a number of lymphocyte-restricted in addition to ubiquitous transcription factors, which may play a role in the transcriptional regulation of the mouse 2B4 gene.


Assuntos
Antígenos CD , Células Matadoras Naturais , Glicoproteínas de Membrana/genética , Regiões Promotoras Genéticas/genética , Receptores Imunológicos/genética , Animais , Sequência de Bases , Clonagem Molecular , Genoma , Camundongos , Dados de Sequência Molecular , Família de Moléculas de Sinalização da Ativação Linfocitária
9.
Immunogenetics ; 50(1-2): 1-7, 1999 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-10541800

RESUMO

Natural killer (NK) cells constitute the third major population of lymphocytes. They possess the inherent capacity to kill various tumor and virally infected cells and mediate the rejection of bone-marrow grafts in lethally irradiated animals. A large family of NK cell receptors belong to the C-type lectin superfamily and are localized to the NK gene complex on Chromosome (Chr) 6 in the mouse and Chr 12 in the human. Genes in the NK gene complex encode type II receptors and examples include the families of NKR-P1, Ly-49, and NKG2 receptors. Examples of other C-type lectin-like NK cell receptors that occur as individual genes are CD94, CD69, and AICL. Here we report the molecular characterization and chromosomal mapping of a human lectin-like transcript (LLT1) expressed on NK, T, and B cells and localized to the NK gene complex within 100 kilobases of CD69. The cDNA encodes a predicted protein of 191 amino acid residues with a transmembrane domain near the N-terminus and an extracellular domain of 132 amino acid residues with similarity to the carbohydrate recognition domain of C-type lectins. The predicted protein of LLT1 shows 59 and 56% similarity to AICL and CD69, respectively. The predicted protein does not contain any intracellular ITIM motifs, suggesting that LLT1 may be involved in mediating activation signals.


Assuntos
Células Matadoras Naturais , Lectinas Tipo C , Lectinas/genética , Linfócitos , Receptores de Superfície Celular/genética , Sequência de Aminoácidos , Sequência de Bases , Mapeamento Cromossômico , Cromossomos Humanos Par 12 , Clonagem Molecular , Humanos , Dados de Sequência Molecular , Homologia de Sequência de Aminoácidos
10.
J Commun Dis ; 23(3): 178-81, 1991 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-1812162

RESUMO

Blood samples from 381 healthy individuals and 236 malaria patients residing in North Madras were studied for glucose-6-phosphate dehydrogenase deficiency. The incidence of this deficiency in this area was found to be 10.05%. Partially deficient healthy females showed a protective trend against malarial infection with the Chi-squared test approaching statistical significance.


Assuntos
Deficiência de Glucosefosfato Desidrogenase/complicações , Malária/complicações , Feminino , Deficiência de Glucosefosfato Desidrogenase/diagnóstico , Humanos , Índia , Malária/imunologia , Masculino
11.
Indian J Malariol ; 28(2): 115-20, 1991 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-1810747

RESUMO

Changes in haematological parameters were studied in 35 Plasmodium vivax infected patients and compared with those in an equal number of normal subjects. Patients showed a high proportion of schizonts of P. vivax (1-2%). Hb, PCV and RBC values were significantly decreased (p less than 0.001) with increasing parasitaemia. Osmotic fragility was slightly increased (15%) when compared to controls and ranged from 0.385-0.405 (50% hypo-osmotic haemolysis given at gm/dl of NaCl) with increasing parasitaemia in the patients. Decreased levels of lymphocyte and increased levels of eosinophils and monocytes were seen in P. vivax infected patients. However, after treatment with chloroquine and primaquine, all the haematological parameters were restored to near normal levels.


Assuntos
Cloroquina/uso terapêutico , Malária Vivax/sangue , Primaquina/uso terapêutico , Contagem de Células Sanguíneas , Hematócrito , Hemoglobinas/análise , Humanos , Índia , Malária Vivax/tratamento farmacológico
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