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1.
Mediators Inflamm ; 2017: 6752756, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28626344

RESUMO

Many neuroinflammatory diseases are characterized by massive immune cell infiltration into the central nervous system. Identifying the underlying mechanisms could aid in the development of therapeutic strategies specifically interfering with inflammatory cell trafficking. To achieve this, we implemented and validated a blood-brain barrier (BBB) model to study chemokine secretion, chemokine transport, and leukocyte trafficking in vitro. In a coculture model consisting of a human cerebral microvascular endothelial cell line and human astrocytes, proinflammatory stimulation downregulated the expression of tight junction proteins, while the expression of adhesion molecules and chemokines was upregulated. Moreover, chemokine transport across BBB cocultures was upregulated, as evidenced by a significantly increased concentration of the inflammatory chemokine CCL3 at the luminal side following proinflammatory stimulation. CCL3 transport occurred independently of the chemokine receptors CCR1 and CCR5, albeit that migrated cells displayed increased expression of CCR1 and CCR5. However, overall leukocyte transmigration was reduced in inflammatory conditions, although higher numbers of leukocytes adhered to activated endothelial cells. Altogether, our findings demonstrate that prominent barrier activation following proinflammatory stimulation is insufficient to drive immune cell recruitment, suggesting that additional traffic cues are crucial to mediate the increased immune cell infiltration seen in vivo during neuroinflammation.


Assuntos
Barreira Hematoencefálica/metabolismo , Movimento Celular/fisiologia , Quimiocina CCL3/metabolismo , Inflamação/metabolismo , Astrócitos/citologia , Astrócitos/metabolismo , Transporte Biológico , Moléculas de Adesão Celular/metabolismo , Linhagem Celular , Impedância Elétrica , Células Endoteliais/citologia , Células Endoteliais/metabolismo , Humanos , Inflamação/genética , Molécula 1 de Adesão Intercelular/metabolismo , Leucócitos/citologia , Leucócitos/metabolismo , Leucócitos Mononucleares/citologia , Leucócitos Mononucleares/metabolismo , Receptores CCR1/genética , Receptores CCR1/metabolismo , Receptores CCR5/genética , Receptores CCR5/metabolismo , Molécula 1 de Adesão de Célula Vascular/metabolismo
2.
Vector Borne Zoonotic Dis ; 15(8): 515-7, 2015 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-26273814

RESUMO

Borrelia miyamotoi, a relapsing fever spirochete, has been found recently in Ixodes ricinus ticks; however, little is known about its spatial distribution and potential local impact on human health. A total of 640 ticks (447 nymphs and 193 adults) collected throughout Portugal were analyzed using two nested PCR protocols, one targeting the flagellin gene and the other the internal transcribed space region between the 5S and the 23S rRNA. As a result, B. miyamotoi was detected, for the first time, in one guesting I. ricinus nymph collected in the Lisboa district. In addition, a prevalence of 11% (71/640) for B. burgdorferi sensu lato was obtained. Even though no human relapsing fever cases due to infection by B. miyamotoi have been reported yet in Portugal, surveillance must be improved to provide better insight into the prevalence and distribution of this spirochete in ticks.


Assuntos
Vetores Aracnídeos/microbiologia , Borrelia/isolamento & purificação , Ixodes/microbiologia , Febre Recorrente/microbiologia , Animais , Sequência de Bases , Borrelia/genética , DNA Bacteriano/química , DNA Bacteriano/genética , Flagelina/genética , Humanos , Dados de Sequência Molecular , Ninfa , Filogenia , Reação em Cadeia da Polimerase , Portugal/epidemiologia , Febre Recorrente/epidemiologia , Análise de Sequência de DNA
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