FP6Реинтеграция2005–2007

DC-SIGN LOCALIZATION · The identification of the cellular localization of DC-SIGN following interaction with HIV and other ligands

6РП — Действия „Мария Кюри“

Период
2005-09-01 → 2007-08-31
Финансиране от ЕС
0 €
Участници
1
Схема
IRG

Линиите свързват координатора с партньорите. За проекти отпреди 2014 г. CORDIS не винаги дава точни координати. Тези точки са на ниво град или държава.

Накратко на български

Протеинът DC-SIGN на повърхността на определени имунни клетки улавя HIV и го пренася към други клетки. Разбирането на този механизъм може да помогне при разработването на стратегии за превенция на HIV/AIDS.

Този кратък обзор е генериран от изкуствен интелект

Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.

Цел на проекта

Dendritic cell specific intercellular adhesion molecule 3 grabbing non-integrin (DC-SIGN, CD209), a C-type lectin on the surface of immature monocyte derived dendritic cells, plays a key role in the transmission of human immunodeficiency virus (HIV) from d endritic cells to T cells. DC-SIGN captures HIV in vitro and transmits it very efficiently to target cells. This can be mimicked in a cell culture model using B-cell lines ectopically expressing DC-SIGN; we have found that only a very limited number of cell types are able to transmit virus. The mechanism of capture/transmission is largely unknown. We are especially interested in the role that internalization of the DC-SIGN/virus complex plays for transmission. This is very difficult to assess in dendritic c ells due to their complex nature. Our cell culture model provides the tools to answer this question. Comparison of cell types that are or are not capable to transmit DC-SIGN associated virus will provide insight into the role internalization plays. Using biochemical and microscopical means we want to identify subcellular localization of DC-SIGN in the different cell systems in response to challenge with virus and/or biological binding partners, such as intercellular adhesion molecules, or mannan. Knowledge about this mechanism would be needed if this early interaction of HIV with dendritic cells in the mucosal tissue should be tackled for an antiretroviral intervention strategy. Interruption of this interaction would provide a possibility for preventive measures against HIV/AIDS.

Оригинален текст от CORDIS (на английски).

Участници

  • FRAUNHOFER-GESELLSCHAFT - FRAUNHOFER INSTITUT FUER ZELLTHERAPIE UND IMMUNOLOGIE · MÜNCHENКоординаторНиво градГермания

Връзки

Данни: CORDIS, © Европейски съюз