| Literature DB >> 33654719 |
Stephanie M Dillon1, Kejun Guo1, Moriah J Castleman1, Mario L Santiago1, Cara C Wilson1.
Abstract
Gut CD4 T cells are major targets of HIV-1 and are massively depleted early during infection. To better understand the mechanisms governing HIV-1-mediated CD4 T cell death, we developed the physiologically-relevant Lamina Propria Aggregate Culture (LPAC) model. The LPAC model is ideal for studying CD4 T cell death induced by clinically-relevant Transmitted/Founder (TF) HIV-1 strains and is also suitable for studying how enteric microbes and soluble factors (e.g., Type I Interferons) impact LP CD4 T cell death and function. Here, we detail the protocol to establish LP CD4 T cell infection using a process of spinoculation, the subsequent evaluation of infection levels using multicolor flow cytometry and the determination of overall LP CD4 T cell death using absolute LP CD4 T cell counts. We also describe the preparation of virus stocks of Transmitted/Founder (TF) HIV-1 infectious molecular clones that were successfully used in the LPAC model.Entities:
Keywords: Death; Gut; HIV-1; Infection; Lamina Propria Aggregate Culture; Lamina Propria Mononuclear cells; T cells
Year: 2020 PMID: 33654719 PMCID: PMC7842360 DOI: 10.21769/BioProtoc.3486
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325