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1.
Proc Natl Acad Sci U S A ; 102(5): 1478-83, 2005 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-15659549

RESUMO

HIV type 1 (HIV-1) was shown to assemble either at the plasma membrane or in the membrane of late endosomes. Now, we report an essential role for human ubiquitin ligase POSH (Plenty of SH3s; hPOSH), a trans-Golgi network-associated protein, in the targeting of HIV-1 to the plasma membrane. Small inhibitory RNA-mediated silencing of hPOSH ablates virus secretion and Gag plasma membrane localization. Reintroduction of native, but not a RING finger mutant, hPOSH restores virus release and Gag plasma membrane localization in hPOSH-depleted cells. Furthermore, expression of the RING finger mutant hPOSH inhibits virus release and induces accumulation of intracellular Gag in normal cells. Together, our results identify a previously undescribed step in HIV biogenesis and suggest a direct function for hPOSH-mediated ubiquitination in protein sorting at the trans-Golgi network. Consequently, hPOSH may be a useful host target for therapeutic intervention.


Assuntos
HIV-1/fisiologia , Ubiquitina-Proteína Ligases/metabolismo , Replicação Viral/fisiologia , Rede trans-Golgi/enzimologia , Membrana Celular/enzimologia , Membrana Celular/virologia , Clonagem Molecular , Produtos do Gene gag/metabolismo , Inativação Gênica , Células HeLa , Humanos , Transporte Proteico , Proteínas Recombinantes/metabolismo , Ubiquitina-Proteína Ligases/genética
2.
Stem Cells Dev ; 13(1): 93-9, 2004 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-15068697

RESUMO

The invasive procedures amniocentesis and chorionic villus sampling (CVS) are routinely applied in pregnancies at risk for fetal abnormalities and the results obtained are the gold standard for prenatal diagnosis. Because these methods of fetal cell procurement involve a 0.5-2% risk for fetal loss, they are recommended mainly in cases at high risk for fetal genetic or cytogenetic abnormalities. The development of a reproducible, reliable, noninvasive method based on retrieval of rare fetal cells from the maternal circulation will render testing feasible for the general population. Despite intensive investigation, a satisfactory, clinically acceptable method has not yet emerged. Several cell types have been targeted to this end, mostly nucleated red blood cells (NRBC), CD34+ hematopoietic progenitors, and trophoblasts. Although these cell types have been unequivocally proven to be present in the maternal circulation, each bears a significant disadvantage, rendering their application in clinical testing currently impossible: NRBC cannot be expanded in culture, thereby ruling out metaphase chromosome analysis, an essential component of prenatal diagnosis. CD34+ cells do posses the potential for in vitro proliferation, however, they have been found to persist in the maternal circulation after delivery, thereby complicating diagnosis in consecutive pregnancies. Trophoblasts are not consistently detected in the maternal circulation. Moreover, due to the lack of a definitive fetal cell marker and a reliable sorting method, foolproof fetal cell identification of any of these cell types is not possible. This report outlines the obstacles that impede development of a method for noninvasive fetal cell sampling for prenatal genetic diagnosis, along with a description of our efforts to analyze simultaneously two fetal blood cell types, NRBC and CD34+ cells in maternal blood during pregnancy, and the problems encountered. This work and that of others lead us to suggest potential future directions to help develop this important technique.


Assuntos
Sangue Fetal/citologia , Troca Materno-Fetal , Diagnóstico Pré-Natal/métodos , Aneuploidia , Antígenos CD34/biossíntese , Divisão Celular , Núcleo Celular/metabolismo , Células Cultivadas , Eritroblastos/metabolismo , Eritrócitos/metabolismo , Feminino , Humanos , Hibridização in Situ Fluorescente , Hibridização de Ácido Nucleico , Gravidez
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