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1.
Nature ; 560(7716): 55-60, 2018 08.
Artigo em Inglês | MEDLINE | ID: mdl-30022166

RESUMO

Acute lymphoblastic leukaemia (ALL) has a marked propensity to metastasize to the central nervous system (CNS). In contrast to brain metastases from solid tumours, metastases of ALL seldom involve the parenchyma but are isolated to the leptomeninges, which is an infrequent site for carcinomatous invasion. Although metastasis to the CNS occurs across all subtypes of ALL, a unifying mechanism for invasion has not yet been determined. Here we show that ALL cells in the circulation are unable to breach the blood-brain barrier in mice; instead, they migrate into the CNS along vessels that pass directly between vertebral or calvarial bone marrow and the subarachnoid space. The basement membrane of these bridging vessels is enriched in laminin, which is known to coordinate pathfinding of neuronal progenitor cells in the CNS. The laminin receptor α6 integrin is expressed in most cases of ALL. We found that α6 integrin-laminin interactions mediated the migration of ALL cells towards the cerebrospinal fluid in vitro. Mice with ALL xenografts were treated with either a PI3Kδ inhibitor, which decreased α6 integrin expression on ALL cells, or specific α6 integrin-neutralizing antibodies and showed significant reductions in ALL transit along bridging vessels, blast counts in the cerebrospinal fluid and CNS disease symptoms despite minimally decreased bone marrow disease burden. Our data suggest that α6 integrin expression, which is common in ALL, allows cells to use neural migratory pathways to invade the CNS.


Assuntos
Sistema Nervoso Central/patologia , Leucemia-Linfoma Linfoblástico de Células Precursoras/patologia , Animais , Anticorpos Neutralizantes/imunologia , Membrana Basal/metabolismo , Barreira Hematoencefálica/metabolismo , Medula Óssea , Movimento Celular , Sistema Nervoso Central/irrigação sanguínea , Sistema Nervoso Central/metabolismo , Líquido Cefalorraquidiano/metabolismo , Circulação Cerebrovascular , Classe I de Fosfatidilinositol 3-Quinases/antagonistas & inibidores , Progressão da Doença , Feminino , Xenoenxertos/imunologia , Xenoenxertos/patologia , Integrina alfa6/imunologia , Integrina alfa6/metabolismo , Laminina/metabolismo , Masculino , Camundongos , Camundongos SCID , Transplante de Neoplasias , Leucemia-Linfoma Linfoblástico de Células Precursoras/enzimologia , Leucemia-Linfoma Linfoblástico de Células Precursoras/metabolismo , Receptores de Laminina/antagonistas & inibidores , Receptores de Laminina/imunologia , Receptores de Laminina/metabolismo , Crânio , Espaço Subaracnóideo
2.
World J Gastroenterol ; 23(42): 7551-7562, 2017 Nov 14.
Artigo em Inglês | MEDLINE | ID: mdl-29204055

RESUMO

AIM: To investigate the therapeutic effect of combined integrin α6ß4-targeted radioimmunotherapy (RIT) and PI3K/mTOR inhibitor BEZ235 in a pancreatic cancer model. METHODS: Phosphorylation of Akt, mTOR, the downstream effectors eukaryotic initiation factor 4E binding protein 1 (4EBP1) and S6 ribosomal protein (S6) were evaluated in BxPC-3 human pancreatic cancer cells treated with Yttrium-90 (90Y) labeled anti-integrin α6ß4 antibody (ITGA6B4) and BEZ235 by western blotting. The cytotoxic effect of BEZ235 was investigated using a colony formation assay. Therapeutic efficacy enhancement by oral BEZ235 administration was assessed using mice bearing BxPC-3 xenograft tumors. Tumor volume measurements and immunohistochemical analyses (cell proliferation marker Ki-67, DNA damage marker p-H2AX and p-4EBP1 staining) of tumors were performed for evaluation of combined treatment with 90Y-ITGA6B4 plus BEZ235, or each arm alone. RESULTS: We found that phosphorylation of Akt (p-Akt), 4EBP1 (p-4EBP1) and S6 (p-S6) was inhibited by BEZ235. Colony formation in BxPC-3 cells was additively suppressed by the combination of 90Y-ITGA6B4 and BEZ235. Pretreatment with BEZ235 before 90Y-ITGA6B4 exposure resulted in significant reduction of cells plating efficiency (PE) (0.54 ± 0.11 vs 2.81 ± 0.14 with 185 kBq/mL 90Y-ITGA6B4 exposure, P < 0.01; 0.39 ± 0.08 vs 1.88 ± 0.09 with 370 kBq/mL 90Y-ITGA6B4 exposure, P < 0.01) when 5 × 103 cells per dish were plated. In vivo, the combined treatment with 90Y-ITGA6B4 plus BEZ235 enhanced the inhibition of tumor growth and statistically significant differences of relative tumor volume were observed for 27 d after the treatment start date when compared with the 90Y-ITGA6B4 single injection treatment (1.03 ± 0.38 vs 1.5 ± 0.15 at Day 27, P < 0.05), and for 41 d when compared with the BEZ235 treatment alone (1.8 ± 0.7 vs 3.14 ± 1.19 at Day 41, P < 0.05). Tumors from treatment groups showed reduction in volumes, decreased Ki-67-positive cells, increased p-H2AX-positive cells and decreased p-4EBP1 expression. CONCLUSION: The therapeutic efficacy of 90Y-ITGA6B4-RIT can be improved by combining with dual PI3K and mTOR inhibitor, BEZ235, in a pancreatic cancer model suggesting potential clinical application.


Assuntos
Anticorpos Monoclonais/uso terapêutico , Antineoplásicos/uso terapêutico , Imidazóis/uso terapêutico , Neoplasias Pancreáticas/radioterapia , Quinolinas/uso terapêutico , Radioisótopos de Ítrio/uso terapêutico , Animais , Antineoplásicos/farmacologia , Linhagem Celular Tumoral , Feminino , Humanos , Imidazóis/farmacologia , Integrina alfa6/imunologia , Integrina beta4/imunologia , Camundongos Nus , Fosfatidilinositol 3-Quinases/metabolismo , Proteínas Proto-Oncogênicas c-akt/metabolismo , Quinolinas/farmacologia , Radioimunoterapia , Transdução de Sinais/efeitos dos fármacos , Ensaios Antitumorais Modelo de Xenoenxerto
3.
Biochem Biophys Res Commun ; 491(3): 629-635, 2017 09 23.
Artigo em Inglês | MEDLINE | ID: mdl-28760342

RESUMO

Acupuncture therapy is performed by applying the needle insertion at discrete cutaneous locations and used for the treatments of diverse symptoms and disorders. In order to elucidate mechanistic basis on how acupuncture stimulation (AS) produces therapeutic effects, it is primarily important to understand tissue responses locally at the acupuncture site (acupoint). Here, we investigated integrin protein as molecular target responding to and integrating AS. Signals of α6 and ß1 integrins were clearly induced at zusanli acupoint 24 h after AS in areas of nuclear clusters around the needle track. Induction levels of integrin were largely reduced by needle insertion at non-acupuncture point or without needle rotation. Phospho-Erk1/2 was initially decreased below the basal level after AS but increased 24 h later. Induction pattern of phospho-Erk1/2 was as similar as that of α6 integrin in its selectivity to needling procedure and tissue distribution. We further found that mRNA expression of P2X3 purinergic receptor was upregulated in the dorsal root ganglion (DRG) after AS, but decreased by the inhibition of Erk1/2 activity at the acupuncture area. Moreover, AS-mediated integrin activation was required for Erk1/2 activation at the acupuncture site and regulation of pain sensitivity in the hind paw. The present results provide a new evidence on acupuncture-specific tissue response in terms of integrin induction, and further suggest that integrin activation may be involved in transmitting mechanosensory signals from the acupoint to afferent nerve fiber.


Assuntos
Terapia por Acupuntura/métodos , Integrina alfa6/imunologia , Integrina beta1/imunologia , Sistema de Sinalização das MAP Quinases/imunologia , Neuralgia/imunologia , Neuralgia/terapia , Pontos de Acupuntura , Animais , Masculino , Mecanotransdução Celular/imunologia , Neuralgia/diagnóstico , Estimulação Física/métodos , Ratos , Ratos Sprague-Dawley , Resultado do Tratamento
4.
J Dermatol ; 44(4): 370-374, 2017 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-27790752

RESUMO

In psoriatic skin, laminin integrity is altered, which could lead to insufficient laminin integrin interactions, leaving the α6-integrin exposed and possibly accessible for autoantibody production. Therefore we investigated the presence of anti-α6-integrin autoantibodies in the serum of patients with psoriasis vulgaris (Ps), psoriatic arthritis (PsA) and rheumatoid arthritis (RA) in comparison with healthy donors. The level of circulating anti-α6-integrin antibodies was determined by enzyme-linked immunoassay using α6-integrin fragments. Antibodies against at least one recombinant fragment were found in approximately 30% of Ps and PsA patients. In contrast, in RA patients, the frequency of antibodies was similar to healthy controls. Our study shows the presence of anti-α6-integrin antibodies in Ps and PsA but not in RA, which could indicate ongoing abnormal processes in the skin. Anti-α6-integrin autoantibodies may contribute to the formation of micro-wounds in the skin and to the characteristic wound-healing phenotype in psoriasis.


Assuntos
Artrite Psoriásica/imunologia , Artrite Reumatoide/imunologia , Autoanticorpos/imunologia , Integrina alfa6/imunologia , Psoríase/imunologia , Adulto , Artrite Psoriásica/sangue , Artrite Reumatoide/sangue , Autoanticorpos/sangue , Ensaio de Imunoadsorção Enzimática , Feminino , Humanos , Integrina alfa6/metabolismo , Laminina/metabolismo , Masculino , Pessoa de Meia-Idade , Psoríase/sangue , Pele/imunologia , Cicatrização/imunologia
6.
Int J Dermatol ; 54(10): e416-23, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26220012

RESUMO

BACKGROUND: Immunofluorescence antigen mapping (IFM), is a newly introduced technique for diagnosis and classification of epidermolysis bullosa (EB) disease. The precise level of skin cleavage can be determined using monoclonal antibodies to EB-specific basement membrane zone protein. OBJECTIVE: To apply IFM technique in diagnosis and classification of EB and to identify utility and limitation of this method in our clinical setting. METHODS: IFM was done according to a described protocol by Pohla-Gubo et al. Monoclonal antibodies used for antigen mapping were against cytokeratin 5, cytokeratin 14, α6 integrin, ß4 integrin, laminin 332, Collagen IV, and Collagen VII. RESULTS: IFM was done for 95 referred patients, compromising 49 females and 46 males, aged 5 days to 45 years (mean = 9.5 years). Ninety cases were diagnosed with EB and classified as follows: EB simplex: (n = 13), junctional EB (n = 14), dystrophic EB (n = 62), and Kindler syndrome (n = 1). Diagnosis was not made in five cases as their specimens contained no blister. Confirmatory genetic analysis was done for five junctional cases from two families with clinical features of laryngo-onycho-cutaneous syndrome. Genetic molecular studies showed nonsense mutations in the last codon of exon 39 of the laminin α3a (LAMA3) gene (p.Gln57X) and a donor splice site mutation in LAMA3 (IVS57+5G>A) in the first and second family, respectively. CONCLUSION: IFM technique is relatively simple to perform, and interpretation of the results is not sophisticated. The proportion of inconclusive results will be decreased if the specimens contain freshly induced blister.


Assuntos
Epidermólise Bolhosa/classificação , Epidermólise Bolhosa/diagnóstico , Imunofluorescência/métodos , Adolescente , Adulto , Anticorpos Monoclonais , Vesícula/diagnóstico , Criança , Pré-Escolar , Códon sem Sentido , Colágeno Tipo IV/imunologia , Colágeno Tipo VII/imunologia , Epidermólise Bolhosa Distrófica/diagnóstico , Epidermólise Bolhosa Simples/diagnóstico , Epidermólise Bolhosa Juncional/diagnóstico , Epidermólise Bolhosa Juncional/genética , Feminino , Humanos , Lactente , Recém-Nascido , Integrina alfa6/imunologia , Integrina beta4/imunologia , Irã (Geográfico) , Queratina-14/imunologia , Queratina-5/imunologia , Laminina/genética , Laminina/imunologia , Masculino , Pessoa de Meia-Idade , Doenças Periodontais/diagnóstico , Transtornos de Fotossensibilidade/diagnóstico , Adulto Jovem
7.
Biomed Res Int ; 2013: 729281, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24455718

RESUMO

Human embryonic stem cells (hESCs) have great potential for clinical therapeutic use. However, relatively little is known of the mechanisms which dictate their specificity of adhesion to substrates through adhesion proteins including integrins. Previous observations demonstrated enhanced clonogenicity in reduced oxygen culture systems. Here, we demonstrated via antibody blocking experiments that αV ß5 and α 6 significantly promoted hESC attachment in 2% O2 only, whereas blockage of CD44 inhibited cell attachment in 21% O2 alone. Immunofluorescence confirmed expression of αV ß5 and CD44 in both 2% O2 and 21% O2 cultured hESCs while flow cytometry revealed significantly higher αV ß5 expression in 2% O2 versus 21% O2 cultured hESCs and higher CD44 expression in 21% O2 versus 2% O2 cultured hESCs. Adhered hESCs following blockage of αV ß5 in 2% O2 displayed a reduction in nuclear colocalisation of Oct-4 and Nanog with little effect observed in 21% O2. Blockage of CD44 had the converse effect with dramatic reductions in nuclear colocalisation of Oct-4 and Nanog in 21% O2 cultured hESC which retained adherence, but not in 2% O2 cultured cells. Identification of oxygen-dependent substrate attachment mechanisms in hESCs has the potential to play a role in the development of novel substrates to improve hESC attachment and culture.


Assuntos
Células-Tronco Embrionárias/metabolismo , Receptores de Hialuronatos/metabolismo , Integrina alfa6/metabolismo , Receptores de Vitronectina/metabolismo , Anticorpos/imunologia , Adesão Celular , Células-Tronco Embrionárias/citologia , Proteínas de Homeodomínio/metabolismo , Humanos , Integrina alfa6/imunologia , Proteína Homeobox Nanog , Fator 3 de Transcrição de Octâmero/metabolismo , Oxigênio/metabolismo , Receptores de Vitronectina/imunologia
8.
Mol Cell Proteomics ; 11(9): 586-95, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22580589

RESUMO

Heterogeneity, shortage of material, and lack of progenitor-specific cell surface markers are major obstacles to elucidating the mechanisms underlying developmental processes. Here we report a proteomics platform that alleviates these difficulties and demonstrate its effectiveness in fractionating heterogeneous cultures of early endoderm derived from human embryonic stem cells. The approach, designated differential cell-capture antibody array, is based on highly parallel, comparative screening of live cell populations using hundreds of antibodies directed against cell-surface antigens. We used this platform to fractionate the hitherto unresolved early endoderm compartment of CXCR4+ cells and identify several endoderm (CD61+ and CD63+) and non-endoderm (CD271+, CD49F+, CD44+ and B2M+) sub-populations. We provide evidence that one of these sub-populations, CD61+, is directly derived from CXCR4+ cells, displays characteristic kinetics of emergence, and exhibits a distinct gene expression profile. The results demonstrate the potential of the cell-capture antibody array as a powerful proteomics tool for detailed dissection of heterogeneous cellular systems.


Assuntos
Antígenos de Superfície/imunologia , Células-Tronco Embrionárias/química , Células-Tronco Embrionárias/citologia , Endoderma/química , Endoderma/citologia , Proteômica , Receptores CXCR4/análise , Anticorpos/imunologia , Biomarcadores/análise , Diferenciação Celular , Linhagem Celular , Linhagem da Célula , Separação Celular , Citometria de Fluxo , Humanos , Receptores de Hialuronatos/análise , Receptores de Hialuronatos/imunologia , Integrina alfa6/análise , Integrina alfa6/imunologia , Integrina beta3/análise , Integrina beta3/imunologia , Proteínas do Tecido Nervoso/análise , Proteínas do Tecido Nervoso/imunologia , Análise de Sequência com Séries de Oligonucleotídeos , Receptores CXCR4/imunologia , Receptores de Fator de Crescimento Neural/análise , Receptores de Fator de Crescimento Neural/imunologia , Tetraspanina 30/análise
9.
PLoS One ; 7(1): e30706, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22295105

RESUMO

Ecotropic viral integration site-1 (EVI1) is one of the candidate oncogenes for human acute myeloid leukemia (AML) with chromosomal alterations at 3q26. High EVI1 expression (EVI1(high)) is a risk factor for AML with poor outcome. Using DNA microarray analysis, we previously identified that integrin α6 (ITGA6) was upregulated over 10-fold in EVI1(high) leukemia cells. In this study, we determined whether the increased expression of ITGA6 is associated with drug-resistance and increased cell adhesion, resulting in poor prognosis. To this end, we first confirmed the expression pattern of a series of integrin genes using semi-quantitative PCR and fluorescence-activated cell sorter (FACS) analysis and determined the cell adhesion ability in EVI1(high) leukemia cells. We found that the adhesion ability of EVI1(high) leukemia cells to laminin increased with the increased expression of ITGA6 and integrin ß4 (ITGB4). The introduction of small-hairpin RNA against EVI1 (shEVI1) into EVI1(high) leukemia cells reduced the cell adhesion ability and downregulated the expression of ITGA6 and ITGB4. In addition, the overexpression of EVI1 in EVI1(low) leukemia cells enhanced their cell adhesion ability and increased the expression of ITGA6 and ITGB4. In a subsequent experiment, the introduction of shRNA against ITGA6 or ITGB4 into EVI1(high) AML cells downregulated their cell adhesion ability; however, the EVI1(high) AML cells transfected with shRNA against ITGA6 could not be maintained in culture. Moreover, treating EVI1(high) leukemia cells with neutralizing antibodies against ITGA6 or ITGB4 resulted in an enhanced responsiveness to anti-cancer drugs and a reduction of their cell adhesion ability. The expression of ITGA6 is significantly elevated in cells from relapsed and EVI1(high) AML cases; therefore, ITGA6 might represent an important therapeutic target for both refractory and EVI1(high) AML.


Assuntos
Proteínas de Ligação a DNA/metabolismo , Resistencia a Medicamentos Antineoplásicos , Regulação Neoplásica da Expressão Gênica , Integrina alfa6/genética , Integrina alfa6/metabolismo , Leucemia Mieloide Aguda/patologia , Fatores de Transcrição/metabolismo , Células 3T3 , Animais , Anticorpos Neutralizantes/imunologia , Bovinos , Adesão Celular , Moléculas de Adesão Celular/metabolismo , Ciclo Celular , Linhagem Celular Tumoral , Colágeno/metabolismo , Regulação para Baixo , Combinação de Medicamentos , Inativação Gênica , Humanos , Integrina alfa6/imunologia , Integrina beta4/genética , Integrina beta4/imunologia , Integrina beta4/metabolismo , Laminina/metabolismo , Leucemia Mieloide Aguda/genética , Proteína do Locus do Complexo MDS1 e EVI1 , Camundongos , Osteoblastos/citologia , Osteoblastos/metabolismo , Proteoglicanas/metabolismo , Proto-Oncogenes , RNA Interferente Pequeno/genética , Recidiva , Calinina
10.
Clin Exp Immunol ; 162(2): 224-36, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-21069937

RESUMO

In this report,we present 15 patients with histological and immunopathologically proven pemphigus vulgaris (PV). After a mean of 80 months since the onset of disease, when evaluated serologically, they had antibodies typical of PV and pemphigoid (Pg). Similarly, 18 patients with bullous pemphigoid (BP) and mucous membrane pemphigoid (MMP) were diagnosed on the basis of histology and immunopathology.After a mean of 60 months since the onset of disease, when their sera were evaluated they were found to have Pg and PV autoantibodies. In both groups of patients the diseases were characterized by a chronic course, which included several relapses and recurrences and were non-responsive to conventional therapy. The major histocompatibility complex class II (MHC II) genes were studied in both groups of patients and phenotypes associated typically with them were observed. Hence, in 33 patients, two different pathogenic autoantibodies were detected simultaneously. The authors provide a computer model to show that each MHC II gene has relevant epitopes that recognize the antigens associated with both diseases. Using the databases in these computer models, the authors present the hypothesis that these two autoantibodies are produced simultaneously due to the phenomena of epitope spreading.


Assuntos
Formação de Anticorpos/imunologia , Autoanticorpos/imunologia , Autoantígenos/imunologia , Genes MHC da Classe II/imunologia , Penfigoide Mucomembranoso Benigno/imunologia , Penfigoide Bolhoso/imunologia , Pênfigo/imunologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Sequência de Aminoácidos , Formação de Anticorpos/genética , Antígenos de Superfície/imunologia , Autoanticorpos/sangue , Autoantígenos/genética , Proteínas de Transporte/genética , Proteínas de Transporte/imunologia , Proteínas do Citoesqueleto/genética , Proteínas do Citoesqueleto/imunologia , Desmogleína 1/imunologia , Desmogleína 3/genética , Desmogleína 3/imunologia , Distonina , Epitopos de Linfócito T/genética , Epitopos de Linfócito T/imunologia , Feminino , Genes MHC da Classe II/genética , Antígenos HLA-DQ/genética , Antígenos HLA-DQ/imunologia , Cadeias beta de HLA-DQ , Antígenos HLA-DR/genética , Antígenos HLA-DR/imunologia , Cadeias HLA-DRB1 , Humanos , Integrina alfa6/genética , Integrina alfa6/imunologia , Integrina beta4/genética , Integrina beta4/imunologia , Queratinócitos/imunologia , Masculino , Pessoa de Meia-Idade , Dados de Sequência Molecular , Proteínas do Tecido Nervoso/genética , Proteínas do Tecido Nervoso/imunologia , Colágenos não Fibrilares/genética , Colágenos não Fibrilares/imunologia , Penfigoide Mucomembranoso Benigno/genética , Penfigoide Bolhoso/genética , Pênfigo/genética , Software , Adulto Jovem , Colágeno Tipo XVII
11.
Blood ; 110(7): 2399-407, 2007 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-17586725

RESUMO

Homing of hematopoietic stem cells (HSCs) into the bone marrow (BM) is a prerequisite for establishment of hematopoiesis during development and following transplantation. However, the molecular interactions that control homing of HSCs, in particular, of fetal HSCs, are not well understood. Herein, we studied the role of the alpha6 and alpha4 integrin receptors for homing and engraftment of fetal liver (FL) HSCs and hematopoietic progenitor cells (HPCs) to adult BM by using integrin alpha6 gene-deleted mice and function-blocking antibodies. Both integrins were ubiquitously expressed in FL Lin(-)Sca-1(+)Kit(+) (LSK) cells. Deletion of integrin alpha6 receptor or inhibition by a function-blocking antibody inhibited FL LSK cell adhesion to its extracellular ligands, laminins-411 and -511 in vitro, and significantly reduced homing of HPCs to BM. In contrast, the anti-integrin alpha6 antibody did not inhibit BM homing of HSCs. In agreement with this, integrin alpha6 gene-deleted FL HSCs did not display any homing or engraftment defect compared with wild-type littermates. In contrast, inhibition of integrin alpha4 receptor by a function-blocking antibody virtually abrogated homing of both FL HSCs and HPCs to BM, indicating distinct functions for integrin alpha6 and alpha4 receptors during homing of fetal HSCs and HPCs.


Assuntos
Células-Tronco Fetais/citologia , Células-Tronco Fetais/metabolismo , Células-Tronco Hematopoéticas/citologia , Células-Tronco Hematopoéticas/metabolismo , Integrina alfa4/metabolismo , Integrina alfa6/metabolismo , Fígado/metabolismo , Envelhecimento/fisiologia , Processamento Alternativo/genética , Animais , Anticorpos/imunologia , Medula Óssea/metabolismo , Adesão Celular , Movimento Celular , Células Cultivadas , Regulação da Expressão Gênica , Fator Estimulador de Colônias de Granulócitos/farmacologia , Células-Tronco Hematopoéticas/efeitos dos fármacos , Integrina alfa6/genética , Integrina alfa6/imunologia , Fígado/citologia , Camundongos , Camundongos Knockout , RNA Mensageiro/genética
12.
Cloning Stem Cells ; 9(2): 191-205, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17579552

RESUMO

Progenitors that can transdifferentiate into cells with hepatic or pancreatic phenotypes can be isolated from experimentally injured salivary glands of rodents. In this study, we isolated progenitors from "uninjured" adult human salivary glands by fluorescence-activated cell sorting using anti-CD49f and anti-Thy-1 antibodies. The sorted cells that were contained in the CD49f+/Thy-1+ fraction showed good proliferation on type I collagen. Single purified progenitor cells in plate culture expressed intracellular laminin, CD49f, Thy-1, and NGF receptor p75 (p75(NGFR)). Immunohistological analysis revealed the expression of Thy-1 and p75(NGFR) in stromal cells in the periductal area of the salivary gland. Under overconfluent conditions in plate culture, cell clusters containing insulin and glucagon-positive cells were occasionally formed. In order to produce differentiated cell clusters with uniform quality, we used a spherical culture system. Autonomous differentiation of cells in clusters into insulin-positive cells was induced in the spherical culture system. We measured C-peptide to estimate the endogenously produced insulin content. The C-peptide content of the spheroid bodies was low (3.5 ng/mg of protein), and they simultaneously expressed the early islet differentiation factor Nkx6.1, proendocrine gene neurogenin3, and ductal cell marker cytokeratin19. The progenitors existing in the interstitium of the salivary gland were able to transdifferentiate into cells with a pancreatic endocrine phenotype.


Assuntos
Diferenciação Celular/fisiologia , Colágeno Tipo I/metabolismo , Regeneração/fisiologia , Glândulas Salivares/citologia , Células-Tronco/citologia , Anticorpos/imunologia , Antígenos de Diferenciação/metabolismo , Peptídeo C/biossíntese , Separação Celular , Células Cultivadas , Glucose/biossíntese , Humanos , Insulina/biossíntese , Integrina alfa6/imunologia , Receptor de Fator de Crescimento Neural/metabolismo , Regeneração/efeitos dos fármacos , Glândulas Salivares/fisiologia , Esferoides Celulares/citologia , Células-Tronco/imunologia , Células-Tronco/fisiologia , Antígenos Thy-1/imunologia
13.
J Invest Dermatol ; 126(12): 2631-6, 2006 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16810295

RESUMO

Mucous membrane pemphigoid (MMP) has several subsets based on target antigens recognized by their sera. MMP and ocular cicatricial pemphigoid (OCP) sera recognize beta4 integrin subunit, oral pemphigoid sera recognize alpha6 integrin subunit, and anti-epiligrin cicatricial pemphigoid sera recognize laminin 5. Our aim is to determine if autoantibodies in the sera of patients with MMP, OCP, and oral pemphigoid (OP) recognize only their target antigens, and to see if this specificity is maintained throughout the clinical course. An immunoblot assay using bovine gingival lysate was used as substrate. Fifteen MMP patients, eight with OCP, and 15 OP patients were studied before therapy and at multiple intervals during the clinical course. Absorption and blocking studies were performed to determine binding specificity. Sera of patients with MMP and OCP recognize only beta4 integrin subunit, and sera of OP patients recognize alpha6 integrin throughout the clinical course. The sera of patients in the subsets of MMP described in this report show adherence and selectivity to target antigen during the entire clinical course, without crossover, interaction, or change. Hence, these subsets of MMP provide an excellent model to study clinical correlation with antigen and antibody specificity, in autoimmunity.


Assuntos
Autoanticorpos/sangue , Oftalmopatias/imunologia , Integrina alfa6/imunologia , Integrina beta4/imunologia , Doenças da Boca/imunologia , Penfigoide Mucomembranoso Benigno/imunologia , Penfigoide Bolhoso/imunologia , Especificidade de Anticorpos , Epitopos , Técnica Indireta de Fluorescência para Anticorpo , Humanos , Immunoblotting , Estudos Longitudinais , Mucosa
14.
Clin Exp Immunol ; 145(1): 28-35, 2006 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-16792670

RESUMO

Mucous membrane pemphigoid (MMP) (also known as cicatricial pemphigoid) is a rare autoimmune mucocutaneous blistering disease that affects mucous membranes derived from stratified squamous epithelium and the skin. A subset of MMP affects only the oral cavity and is referred to as the oral pemphigoid (OP). MMP and OP are characterized by subepithelial vesicles on histology and in vivo deposition of immunoglobulins and complement at the basement membrane zone (BMZ) on immunopathology. Previous studies have shown that sera of patients with MMP bind to human integrin beta4, while sera of patients with oral pemphigoid bind to the integrin alpha6 component of the heterodimer. The prognosis in MMP is grave but excellent in OP. In this study we compare the binding of sera from patients with OP from Boston, MA, USA to Naples, Italy, and attempt to identify an epitope to which the anti-integrin alpha6 human autoantibody binds. Our results indicate that the sera from Boston and Naples are identical in their reactivity. They recognize a fragment I (AA 23-462) and its subfragment IB (AA 217-462) only, in the human integrin alpha6 molecule. Blocking studies, immunoprecipitation and immunoabsorbtion studies confirm the presence of this single 245 AA region. Antibodies to subfragment IB cause BMZ separation in organ culture using normal human oral mucosa as substrate. This preliminary study indicates that patients on both continents may have similar reactivity and suggests that an intercontinental study group could be established to advance our understanding of the pathogenesis of OP and the biology of anti-alpha6 integrin autoantibodies.


Assuntos
Autoanticorpos/imunologia , Autoantígenos/sangue , Doenças da Boca/imunologia , Mucosa Bucal/imunologia , Penfigoide Bolhoso/imunologia , Animais , Western Blotting/métodos , Estudos de Casos e Controles , Epitopos/análise , Humanos , Fragmentos de Imunoglobulinas/análise , Fragmentos de Imunoglobulinas/imunologia , Integrina alfa6/imunologia , Itália , Técnicas de Cultura de Órgãos , Coelhos , Estados Unidos
15.
Exp Eye Res ; 83(3): 543-53, 2006 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-16631165

RESUMO

The extracellular microenvironment regulates lacrimal gland acinar cell secretion. Culturing isolated rabbit lacrimal gland acinar cells on different extracellular matrix proteins revealed that laminin enhances carbachol-stimulated secretion to a greater extent than other extracellular matrix proteins investigated. Furthermore, immunofluorescence indicated that integrin subunits, potentially functioning as laminin receptors are present in acinar cells. Among these, the integrin alpha6 and beta1 subunit mRNA expression was also confirmed by RT-PCR and sequence analysis. Secretion assays, which measured beta-hexosaminidase activity released in the culture media, demonstrated that function-blocking integrin alpha6 and beta1 monoclonal antibodies (mAbs) induce a rapid, transient and dose-dependent secretory response in cultured cells. To determine the intracellular pathways by which integrin alpha6 and beta1 mAbs could induce secretion, selected second messenger molecules were inhibited. Although inhibitors of protein kinase C and IP(3)-induced Ca(2+) mobilization attenuated carbachol-stimulated secretion, no effect on integrin mAb-induced release was observed. In addition, protein tyrosine kinases do not appear to have a role in transducing signals arising from mAb interactions. Our data clearly demonstrate, though, that cell adhesion through integrins regulates secretion from lacrimal gland acinar cells. The fact that the integrin mAbs affect the cholinergic response differently and that the integrin beta1 mAb secretion, but not the alpha6, was attenuated by the phosphatase inhibitor, sodium orthovanadate, suggests that each subunit utilizes separate intracellular signaling pathways to induce exocytosis. The results also indicate that the secretory response triggered by the beta1 integrin mAb is generated through dephosphorylation events.


Assuntos
Matriz Extracelular/metabolismo , Integrinas/metabolismo , Aparelho Lacrimal/metabolismo , Laminina/metabolismo , Animais , Anticorpos Monoclonais/farmacologia , Cálcio/metabolismo , Carbacol/farmacologia , Adesão Celular , Células Cultivadas , Agonistas Colinérgicos/farmacologia , Integrina alfa6/genética , Integrina alfa6/imunologia , Integrina alfa6/metabolismo , Integrina beta1/genética , Integrina beta1/imunologia , Integrina beta1/metabolismo , Integrinas/genética , Integrinas/imunologia , Aparelho Lacrimal/citologia , Laminina/farmacologia , Monoéster Fosfórico Hidrolases/antagonistas & inibidores , Monoéster Fosfórico Hidrolases/metabolismo , Proteína Quinase C/antagonistas & inibidores , Proteína Quinase C/metabolismo , Proteínas Quinases/metabolismo , RNA Mensageiro/análise , Coelhos , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Vanadatos/farmacologia
16.
Int Arch Allergy Immunol ; 140(2): 113-20, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16569934

RESUMO

BACKGROUND: Albumin is known to induce chemokinesis and facilitate chemotaxis of human granulocytes in the Boyden chamber assay, but its mechanisms of action remain obscure. We have previously found that IL-2 inhibits albumin-stimulated eosinophil migration. The aim of this study was to identify the mechanisms behind the effects of albumin and IL-2 on the migration of human eosinophils. METHODS: Purified eosinophils were preincubated with inhibitors of signal transduction molecules before incubation with or without albumin and IL-2. The migration assay was performed in a 48-well microchemotaxis chamber. The effect of albumin and IL-2 on cell size and on the surface expression of adhesion molecules was studied with flow cytometry. RESULTS: Albumin-stimulated migration was inhibited by the PI3-kinase inhibitors wortmannin and LY-294002, but not by the PKC inhibitor RO-31-8220. IL-2 had no effect after preincubation with wortmannin or LY-294002. In contrast, the inhibitory effect of IL-2 remained after preincubation with RO-31-8220. Albumin increased the cell size as measured by forward scatter, and the expression of CD49d and CD49f decreased after incubation with albumin. IL-2 affected neither the expression of adhesion molecules nor the forward scatter. CONCLUSIONS: The stimulation of eosinophil migration by albumin is mediated by PI3-kinase, and the increase in cell size caused by albumin indicates activation of the cells. Decreased expression of CD49d and CD49f by albumin may diminish the adhesiveness of the cells, which in turn may facilitate migration. These are novel findings that indicate an active role for albumin in eosinophil migration.


Assuntos
Quimiotaxia de Leucócito/imunologia , Eosinófilos/imunologia , Integrina alfa4/biossíntese , Integrina alfa6/biossíntese , Fosfatidilinositol 3-Quinases/metabolismo , Albumina Sérica/farmacologia , Adulto , Androstadienos/farmacologia , Adesão Celular/efeitos dos fármacos , Adesão Celular/imunologia , Tamanho Celular/efeitos dos fármacos , Quimiotaxia de Leucócito/efeitos dos fármacos , Cromonas/farmacologia , Relação Dose-Resposta Imunológica , Eosinófilos/citologia , Citometria de Fluxo , Humanos , Indóis/farmacologia , Integrina alfa4/imunologia , Integrina alfa6/imunologia , Interleucina-2/antagonistas & inibidores , Interleucina-2/imunologia , Interleucina-2/farmacologia , Pessoa de Meia-Idade , Morfolinas/farmacologia , Inibidores de Fosfoinositídeo-3 Quinase , Inibidores de Proteínas Quinases/farmacologia , Albumina Sérica/antagonistas & inibidores , Albumina Sérica/imunologia , Transdução de Sinais/efeitos dos fármacos , Wortmanina
17.
J Immunol ; 176(3): 1968-77, 2006 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-16424229

RESUMO

Oral pemphigoid (OP) is a rare chronic autoimmune disease characterized by blisters and erosive lesions in the oral mucosa. We identified an epitope for the binding of OP autoantibodies within the integrin alpha6 subunit, by cloning four overlapping fragments (A, B, C, and D). Immunoperoxidase studies demonstrated that all of the fragments were present in the oral mucosa. Sera of 20 patients with active OP were studied. All sera bound to integrin alpha6 in DU145 cell lysate by immunoprecipitation and immunoblot assay. The same sera bound only to fragment A and its subfragment A2 on an immunoblot assay. The specificity of the binding was further characterized by blocking and cross-absorption studies. A 14-aa synthetic peptide A2.1, within fragment A2, bound to all the test sera. The sera in this study bound to only one epitope. Controls were sera samples from 10 healthy volunteers and 40 patients with other variants of mucous membrane pemphigoid and mAb GoH3 and BQ16 to integrin alpha6. Control sera did not bind to the full-length integrin alpha6 subunit nor any of the cloned fragments. The OP patient sera and immunoaffinity-purified OP sera, rabbit antisera against fragments A and A2, and mAb GoH3 produced basement membrane separation of oral mucosa in organ culture. This study identifies a peptide within the extracellular domain of integrin alpha6 molecule, to which Abs in the sera from patients with OP bind, and which may play an important role in the pathogenesis of OP.


Assuntos
Autoanticorpos/metabolismo , Membrana Basal/imunologia , Sítios de Ligação de Anticorpos , Epitopos/metabolismo , Integrina alfa6/imunologia , Doenças da Boca/imunologia , Penfigoide Bolhoso/imunologia , Subunidades Proteicas/imunologia , Autoanticorpos/fisiologia , Membrana Basal/patologia , Epitopos/imunologia , Espaço Extracelular/imunologia , Espaço Extracelular/metabolismo , Humanos , Técnicas Imunoenzimáticas , Fragmentos de Imunoglobulinas/imunologia , Integrina alfa6/metabolismo , Microscopia Confocal , Doenças da Boca/patologia , Mucosa Bucal/imunologia , Mucosa Bucal/patologia , Técnicas de Cultura de Órgãos , Penfigoide Bolhoso/metabolismo , Penfigoide Bolhoso/patologia , Subunidades Proteicas/metabolismo
18.
Ann N Y Acad Sci ; 1051: 104-10, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-16126949

RESUMO

Bullous pemphigoid (BP) is characterized immunologically by tissue-bound and circulating autoantibodies targeting the hemidesmosomal proteins BP230 and BP180. Recent evidence suggests a pathophysiological role for autoantibodies against alpha6 integrin in the subepidermal blister formation of oral pemphigoid. The objective of our study was to investigate the presence of anti-alpha6 integrin antibodies in patients with classical BP. The autoantibody profiles of 30 patients with BP, 10 patients with pemphigus vulgaris, and 20 healthy persons were identified. With the use of PeptideStructure and PlotStructure software, four different antigenic epitopes for alpha6 integrin were predicted, and their fusion recombinant constructs were prepared in an E. coli expression system. Sera were tested for alpha6 integrin autoantibodies by an ELISA technique. Altogether, 52% of the patients with BP displayed circulating antibodies against at least one recombinant protein. Our findings provide the first evidence for the presence of anti-alpha6 integrin antibodies in patients with classical BP.


Assuntos
Autoanticorpos/sangue , Integrina alfa6/imunologia , Penfigoide Bolhoso/imunologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade
19.
Methods Mol Biol ; 289: 87-96, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-15502173

RESUMO

Recent work from our laboratory has led to the development and validation of fluorescence-activated cell sorting (FACS)-based techniques to prospectively isolate viable keratinocyte stem cells from both human and murine skin. Here we describe a step-by-step method to apply our technique to isolate epidermal keratinocytes from skin tissue, process them for immunofluorescent staining for cell surface markers, and subject them to fluorescence-activated cell sorting to obtain the stem, transient amplifying, and early differentiating keratinocyte fractions. These viable cells can then be placed into culture for further analysis or directly into keratinocyte assays, such as organotypic cultures or in vivo transplantation. This method will be useful for the complete biological characterization of keratinocyte progenitors with respect to wound healing, carcinogenesis, and therapeutic manipulation.


Assuntos
Antígenos CD/imunologia , Antígenos de Diferenciação de Linfócitos B/imunologia , Citometria de Fluxo/métodos , Integrina alfa6/imunologia , Queratinócitos/citologia , Células-Tronco/citologia , Animais , Células Cultivadas , Humanos , Queratinócitos/imunologia , Camundongos , Receptores da Transferrina , Células-Tronco/imunologia
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