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1.
J Biol Chem ; 291(6): 3030-42, 2016 Feb 05.
Artigo em Inglês | MEDLINE | ID: mdl-26601958

RESUMO

UBE2W ubiquitinates N termini of proteins rather than internal lysine residues, showing a preference for substrates with intrinsically disordered N termini. The in vivo functions of this intriguing E2, however, remain unknown. We generated Ube2w germ line KO mice that proved to be susceptible to early postnatal lethality without obvious developmental abnormalities. Although the basis of early death is uncertain, several organ systems manifest changes in Ube2w KO mice. Newborn Ube2w KO mice often show altered epidermal maturation with reduced expression of differentiation markers. Mirroring higher UBE2W expression levels in testis and thymus, Ube2w KO mice showed a disproportionate decrease in weight of these two organs (~50%), suggesting a functional role for UBE2W in the immune and male reproductive systems. Indeed, Ube2w KO mice displayed sustained neutrophilia accompanied by increased G-CSF signaling and testicular vacuolation associated with decreased fertility. Proteomic analysis of a vulnerable organ, presymptomatic testis, showed a preferential accumulation of disordered proteins in the absence of UBE2W, consistent with the view that UBE2W preferentially targets disordered polypeptides. These mice further allowed us to establish that UBE2W is ubiquitously expressed as a single isoform localized to the cytoplasm and that the absence of UBE2W does not alter cell viability in response to various stressors. Our results establish that UBE2W is an important, albeit not essential, protein for early postnatal survival and normal functioning of multiple organ systems.


Assuntos
Epiderme , Anormalidades da Pele , Enzimas de Conjugação de Ubiquitina , Animais , Epiderme/anormalidades , Epiderme/enzimologia , Epiderme/imunologia , Transtornos Leucocíticos/congênito , Transtornos Leucocíticos/enzimologia , Transtornos Leucocíticos/genética , Transtornos Leucocíticos/imunologia , Masculino , Camundongos , Camundongos Knockout , Anormalidades da Pele/enzimologia , Anormalidades da Pele/genética , Anormalidades da Pele/imunologia , Testículo/enzimologia , Testículo/imunologia , Timo/enzimologia , Timo/imunologia , Enzimas de Conjugação de Ubiquitina/deficiência , Enzimas de Conjugação de Ubiquitina/imunologia
2.
Am J Pathol ; 184(1): 200-13, 2014 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-24211111

RESUMO

Excessive neutrophil migration across the pulmonary endothelium into the lung and release of oxidants and proteases are key elements in pathogenesis of acute lung injury. Previously, we identified protein kinase C-delta (PKCδ) as an important regulator of proinflammatory signaling in human neutrophils and demonstrated that intratracheal instillation of a TAT-conjugated PKCδ inhibitory peptide (PKCδ-TAT) is lung protective in a rat model of sepsis-induced indirect pulmonary injury (cecal ligation and puncture). In the present study, intratracheal instillation of this PKCδ inhibitor resulted in peptide distribution throughout the lung parenchyma and pulmonary endothelium and decreased neutrophil influx, with concomitant attenuation of sepsis-induced endothelial ICAM-1 and VCAM-1 expression in this model. To further delineate the role of PKCδ in regulating neutrophil migration, we used an in vitro transmigration model with human pulmonary microvascular endothelial cells (PMVECs). Consistent with in vivo findings, inhibition of PMVEC PKCδ decreased IL-1ß-mediated neutrophil transmigration. PKCδ regulation was stimulus-dependent; PKCδ was required for transmigration mediated by IL-1ß and fMLP (integrin-dependent), but not IL-8 (integrin-independent). PKCδ was essential for IL-1ß-mediated neutrophil adherence and NF-κB-dependent expression of ICAM-1 and VCAM-1. In PMVECs, IL-1ß-mediated production of ROS and activation of redox-sensitive NF-κB were PKCδ dependent, suggesting an upstream signaling role. Thus, PKCδ has an important role in regulating neutrophil-endothelial cell interactions and recruitment to the inflamed lung.


Assuntos
Lesão Pulmonar Aguda/enzimologia , Células Endoteliais/enzimologia , Doenças do Sistema Imunitário/enzimologia , Transtornos Leucocíticos/enzimologia , Proteína Quinase C-delta/metabolismo , Migração Transendotelial e Transepitelial/fisiologia , Lesão Pulmonar Aguda/imunologia , Lesão Pulmonar Aguda/patologia , Animais , Linhagem Celular , Modelos Animais de Doenças , Humanos , Imuno-Histoquímica , Masculino , Pneumonia/enzimologia , Pneumonia/imunologia , Pneumonia/patologia , RNA Interferente Pequeno , Ratos , Ratos Sprague-Dawley
3.
Shock ; 39(4): 389-96, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23481491

RESUMO

A reduction of the neutrophil migration into the site of infection during cecal ligation and puncture-induced sepsis increases host mortality. Inhibition of heme oxygenase (HO) prevents this neutrophil paralysis and improves host survival in the cecal ligation and puncture model. Taking into account that almost 50% of all sepsis cases are a consequence of pneumonia, we designed the present study to determine the role of HO in an experimental model of pneumonia-induced sepsis. The objective of this study was to evaluate whether the inhibition of HO improves the outcome and pathophysiologic changes of sepsis induced by an intratracheal instillation of Klebsiella pneumoniae. The pretreatment of mice subjected to pneumonia-induced sepsis with ZnDPBG (zinc deuteroporphyrin 2,4-bis glycol), a nonspecific HO inhibitor, increased the number of neutrophils in the bronchoalveolar spaces, reduced the bacterial load at the site of infection, and prevented the upregulation of CD11b and the downregulation of CXCR2 on blood neutrophils. Moreover, the pretreatment with ZnDPBG decreased alveolar collapse, attenuating the deleterious changes in pulmonary mechanics and gas exchanges and, as a consequence, improved the survival rate of mice from 0% to ∼20%. These results show that heme oxygenase is involved in the pathophysiology of pneumonia-induced sepsis and suggest that HO inhibitors could be helpful for the management of this disease.


Assuntos
Bacteriemia/enzimologia , Heme Oxigenase (Desciclizante)/antagonistas & inibidores , Doenças do Sistema Imunitário/enzimologia , Infecções por Klebsiella/enzimologia , Transtornos Leucocíticos/enzimologia , Pneumonia Bacteriana/enzimologia , Alvéolos Pulmonares/enzimologia , Lesão Pulmonar Aguda/prevenção & controle , Animais , Bacteriemia/microbiologia , Brônquios/enzimologia , Quimiocinas/metabolismo , Creatina Quinase Forma MB/metabolismo , Citocinas/metabolismo , Deuteroporfirinas/farmacologia , Inibidores Enzimáticos/farmacologia , Infecções por Klebsiella/microbiologia , Klebsiella pneumoniae , Camundongos , Pneumonia Bacteriana/microbiologia , Receptores de Interleucina-8B/metabolismo
4.
Methods Mol Biol ; 412: 525-30, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-18453132

RESUMO

Polymorphonuclear neutrophils (PMN) represent the dominant cell in the acute response to microbial infection. Effective antimicrobial activity reflects the combined action of soluble agents in plasma with PMN-derived reactive oxygen species and granule proteins, including the azurophilic granule protein myeloperoxidase (MPO). The inhibition or absence of the MPO-H2O2-halide system results in marked reduction in PMN killing of a variety of microbes, implicating its relative prominence in the hierarchy of PMN antimicrobial systems. Although the most profound clinical defects are manifested in patients lacking the capacity to generate reactive oxygen species, as seen in chronic granulomatous disease, an inherited deficiency of MPO can also increase the frequency or severity of clinical infections. As a first step in evaluating the MPO-dependent system, determination of peroxidase activity of isolated leukocytes enriched for PMN coupled with histochemical staining of leukocytes allows assessment of functional MPO within PMN. Immunoblotting of the isolated leukocytes for MPO provides additional information, supplying insight into the molecular basis of the observed absence of functional enzyme.


Assuntos
Técnicas e Procedimentos Diagnósticos , Transtornos Leucocíticos/diagnóstico , Peroxidase/deficiência , Western Blotting , Humanos , Transtornos Leucocíticos/enzimologia , Peroxidase/metabolismo , Espectrofotometria/métodos , Coloração e Rotulagem/métodos
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