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严重组织损伤诱导 T 细胞死亡的巨噬细胞-T 细胞共培养模型。

A macrophage-T cell coculture model for severe tissue injury-induced T cell death.

机构信息

Institute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, Munich, Germany.

Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.

出版信息

STAR Protoc. 2021 Dec 1;2(4):100983. doi: 10.1016/j.xpro.2021.100983. eCollection 2021 Dec 17.

DOI:10.1016/j.xpro.2021.100983
PMID:34927092
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8646263/
Abstract

A key observation of tissue injury, such as stroke and burn, is a state of systemic immunosuppression characterized by loss of T cells and rise of infections. Here, we present an model for cell-cell interactions between innate (macrophages) and adaptive (T cells) immune cells. This protocol facilitates bone marrow-derived macrophages (BMDMs) and splenic T cells in a coculture model. The procedure mimics injury-induced T cell death, which is driven by inflammasome activation in macrophages. For complete details on the use and execution of this protocol, please refer to Roth et al. (2021).

摘要

组织损伤(如中风和烧伤)的一个关键观察结果是全身免疫抑制状态,其特征是 T 细胞减少和感染增加。在这里,我们提出了一种固有(巨噬细胞)和适应性(T 细胞)免疫细胞之间细胞-细胞相互作用的模型。该方案促进了骨髓来源的巨噬细胞(BMDM)和脾 T 细胞在共培养模型中的共培养。该程序模拟了由巨噬细胞中炎症小体激活驱动的损伤诱导的 T 细胞死亡。有关此方案使用和执行的完整详细信息,请参阅 Roth 等人。(2021 年)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b989/8646263/bf1f16479dcb/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b989/8646263/2778673c0bca/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b989/8646263/24efd36b8ed3/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b989/8646263/27efee5d1fd9/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b989/8646263/49ee3911cdaf/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b989/8646263/454909ae1e8d/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b989/8646263/bf1f16479dcb/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b989/8646263/2778673c0bca/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b989/8646263/24efd36b8ed3/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b989/8646263/27efee5d1fd9/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b989/8646263/49ee3911cdaf/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b989/8646263/454909ae1e8d/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b989/8646263/bf1f16479dcb/gr5.jpg

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4
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iScience. 2023 Apr 27;26(5):106758. doi: 10.1016/j.isci.2023.106758. eCollection 2023 May 19.
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4
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5
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Cancer Discov. 2020 Dec;10(12):1842-1853. doi: 10.1158/2159-8290.CD-20-0047. Epub 2020 Aug 14.
6
Influence of the culture medium on the production of nitric oxide and expression of inducible nitric oxide synthase by activated macrophages .培养基对活化巨噬细胞产生一氧化氮及诱导型一氧化氮合酶表达的影响
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7
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8
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J Immunol. 2006 Jun 1;176(11):6523-31. doi: 10.4049/jimmunol.176.11.6523.