发布: 2016年11月20日第6卷第22期 DOI: 10.21769/BioProtoc.2004 浏览次数: 10296
评审: Kristopher MarjonVaibhav B ShahValeria Lulla
相关实验方案
基于Flow-FISH的流式细胞术检测终止型与延伸型HIV-1转录本阳性细胞的定量分析
Shirley Man [...] Neeltje A. Kootstra
2025年07月20日 1094 阅读
Abstract
The aim of this protocol is to describe how to measure and quantify the amount of HIV-1 particles and dextran molecules internalized in human monocyte derived dendritic cells (MDDCs), using three different techniques: flow cytometry, quantitative PCR and confocal microscopy.
Background
This protocol was developed in order to assess the changes of HIV-1 internalization upon disruption of actin nucleation in human monocyte derived dendritic cells. Following a shRNA screen to identify genes important for HIV-1 transfer from dendritic cells to T cells, we observed that a disruption of actin nucleation leads to a switch from actin rich dendrites to blebs, due to an excess of actomyosin contraction. As a consequence, a decrease of HIV-1 transfer and an increase of HIV-1 internalization due to bleb retraction-driven macropinocytosis were observed. We concluded that effectors of actin nucleation and stabilization were key to maintain HIV-1 on actin-rich dendrites and to limit its endocytosis, for efficient transfer to T lymphocytes (Menager and Littman, 2016).
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文章信息
版权信息
© 2016 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Ménager, M. M. and Littman, D. R. (2016). Quantitative Measurements of HIV-1 and Dextran Capture by Human Monocyte-derived Dendritic Cells (MDDCs). Bio-protocol 6(22): e2004. DOI: 10.21769/BioProtoc.2004.
分类
细胞生物学 > 细胞成像 > 荧光
免疫学 > 宿主防御 > 人
细胞生物学 > 基于细胞的分析方法 > 流式细胞术
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