• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

用于抗原呈递分析的体外骨髓来源树突状细胞(BMDC)生成

In Vitro Bone Marrow-Derived Dendritic Cells (BMDC) Generation for Antigen Presentation Assay.

作者信息

Singh Sudhakar, Tehseen Azeez, Iqbal Mohammed Shaaz, Sehrawat Sharvan

机构信息

Indian Institute of Science Education and Research, Mohali, India.

出版信息

Bio Protoc. 2025 Apr 20;15(8):e5278. doi: 10.21769/BioProtoc.5278.

DOI:10.21769/BioProtoc.5278
PMID:40291430
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12021583/
Abstract

Dendritic cells (DC) are sentinel cells of the immune system that process and present antigens to activate T cells, thus serving to bridge the innate and adaptive immune systems. DCs are particularly efficient at cross-presentation whereby exogenously acquired antigens are processed and presented in context with MHCI molecules to activate CD8 T cells. Assaying antigen presentation by DCs is a critical parameter in assessing immune functionality. However, the low abundance of bona fide DCs within the lymphoid compartments limits the utility of such assays. An alternative approach employing the culturing of bone marrow cells in the presence of factors needed for DC lineage commitment can result in the differentiation of bone marrow dendritic cells (BMDCs). This protocol details the process of in vitro generation of BMDCs and demonstrates their subsequent utility in antigen presentation assays. The protocol described can be adapted to various conditions and antigens. Key features • BMDCs can serve as surrogate antigen-presenting cells (APCs) for assessing in vitro and in vivo antigen presentation. • Co-culture of antigen-stimulated BMDCs with CFSE-labeled T cells can help quantify the responsiveness of both the antigen presenters and responders. • In vivo analysis of antigen presentation by BMDCs can be assessed using an adoptive transfer approach. • CFSE labeling can help track in vivo the fate of adoptively transferred BMDCs as well as T cells.

摘要

树突状细胞(DC)是免疫系统的哨兵细胞,其处理并呈递抗原以激活T细胞,从而在固有免疫系统和适应性免疫系统之间起到桥梁作用。DC在交叉呈递方面特别高效,即外源性获取的抗原被处理并与MHC I类分子一起呈递,以激活CD8 T细胞。检测DC的抗原呈递是评估免疫功能的一个关键参数。然而,淋巴组织中真正DC的低丰度限制了此类检测的实用性。另一种方法是在存在DC谱系定向所需因子的情况下培养骨髓细胞,这可导致骨髓树突状细胞(BMDC)的分化。本方案详细介绍了体外生成BMDC的过程,并展示了它们在抗原呈递检测中的后续用途。所描述的方案可适用于各种条件和抗原。关键特性 • BMDC可作为替代抗原呈递细胞(APC),用于评估体外和体内的抗原呈递。 • 将抗原刺激的BMDC与CFSE标记的T细胞共培养,有助于量化抗原呈递细胞和反应细胞的反应性。 • 可使用过继转移方法评估BMDC在体内的抗原呈递情况• CFSE标记有助于在体内追踪过继转移的BMDC以及T细胞的命运。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29f1/12021583/9a112ea9757c/BioProtoc-15-8-5278-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29f1/12021583/a43414af575b/BioProtoc-15-8-5278-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29f1/12021583/2450e8a74725/BioProtoc-15-8-5278-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29f1/12021583/8b8e405ba8d2/BioProtoc-15-8-5278-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29f1/12021583/bb4e6787bea0/BioProtoc-15-8-5278-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29f1/12021583/caf5473b0e72/BioProtoc-15-8-5278-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29f1/12021583/9a112ea9757c/BioProtoc-15-8-5278-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29f1/12021583/a43414af575b/BioProtoc-15-8-5278-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29f1/12021583/2450e8a74725/BioProtoc-15-8-5278-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29f1/12021583/8b8e405ba8d2/BioProtoc-15-8-5278-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29f1/12021583/bb4e6787bea0/BioProtoc-15-8-5278-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29f1/12021583/caf5473b0e72/BioProtoc-15-8-5278-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29f1/12021583/9a112ea9757c/BioProtoc-15-8-5278-g006.jpg

相似文献

1
In Vitro Bone Marrow-Derived Dendritic Cells (BMDC) Generation for Antigen Presentation Assay.用于抗原呈递分析的体外骨髓来源树突状细胞(BMDC)生成
Bio Protoc. 2025 Apr 20;15(8):e5278. doi: 10.21769/BioProtoc.5278.
2
A Comprehensive Experimental Guide to Studying Cross-Presentation in Dendritic Cells In Vitro.体外研究树突状细胞交叉呈递的综合实验指南
Curr Protoc Immunol. 2020 Dec;131(1):e115. doi: 10.1002/cpim.115.
3
Infection of mouse bone marrow-derived dendritic cells with recombinant adenovirus vectors leads to presentation of encoded antigen by both MHC class I and class II molecules-potential benefits in vaccine design.用重组腺病毒载体感染小鼠骨髓来源的树突状细胞会导致编码抗原通过MHC I类和II类分子呈递,这在疫苗设计中具有潜在益处。
Vaccine. 2002 Dec 13;21(3-4):231-42. doi: 10.1016/s0264-410x(02)00448-6.
4
Outer membrane vesicles engineered to express membrane-bound antigen program dendritic cells for cross-presentation to CD8 T cells.经工程改造表达膜结合抗原的外膜囊泡可对树突状细胞进行交叉呈递,以激活 CD8 T 细胞。
Acta Biomater. 2019 Jun;91:248-257. doi: 10.1016/j.actbio.2019.04.033. Epub 2019 Apr 17.
5
Characterization of regulatory dendritic cells differentiated from the bone marrow of UV-irradiated mice.辐射小鼠骨髓来源的调节性树突状细胞的鉴定。
Immunology. 2013 Dec;140(4):399-412. doi: 10.1111/imm.12145.
6
Prevention of alloimmune rejection using XBP1-deleted bone marrow-derived dendritic cells in heart transplantation.使用 XBP1 缺失的骨髓源性树突状细胞预防心脏移植中的同种免疫排斥。
J Heart Lung Transplant. 2022 Dec;41(12):1660-1671. doi: 10.1016/j.healun.2022.08.010. Epub 2022 Aug 20.
7
The relative efficiency of acquisition of MHC:peptide complexes and cross-presentation depends on dendritic cell type.主要组织相容性复合体(MHC):肽复合物的获取效率和交叉呈递效率取决于树突状细胞的类型。
J Immunol. 2008 Sep 1;181(5):3212-20. doi: 10.4049/jimmunol.181.5.3212.
8
Characterization of murine dendritic cell line JAWS II and primary bone marrow-derived dendritic cells in Chlamydia muridarum antigen presentation and induction of protective immunity.鼠源树突状细胞系JAWS II和原发性骨髓来源树突状细胞在鼠衣原体抗原呈递及诱导保护性免疫中的特性研究
Infect Immun. 2008 Jun;76(6):2392-401. doi: 10.1128/IAI.01584-07. Epub 2008 Mar 24.
9
Dendritic Cell Migration and Antigen Presentation Are Coordinated by the Opposing Functions of the Tetraspanins CD82 and CD37.树突状细胞迁移和抗原呈递由四跨膜蛋白CD82和CD37的相反功能协调。
J Immunol. 2016 Feb 1;196(3):978-87. doi: 10.4049/jimmunol.1500357. Epub 2016 Jan 4.
10
D609 Suppresses Antituberculosis Response by Regulating Dendritic Cells Antigen Presentation.D609通过调节树突状细胞抗原呈递抑制抗结核反应。
Immun Inflamm Dis. 2024 Dec;12(12):e70103. doi: 10.1002/iid3.70103.

本文引用的文献

1
Rab8a restores diverse innate functions in CD11cCD11b dendritic cells from aged mice.Rab8a 恢复了老年小鼠中 CD11cCD11b 树突状细胞的多种固有功能。
Nat Commun. 2024 Nov 27;15(1):10300. doi: 10.1038/s41467-024-54757-2.
2
Myeloid derived suppressor cells potentiate virus-specific memory CD8 T cell response.髓系来源的抑制细胞增强病毒特异性记忆 CD8 T 细胞应答。
Microbes Infect. 2024 Mar-Apr;26(3):105277. doi: 10.1016/j.micinf.2023.105277. Epub 2023 Dec 14.
3
A catalytically inactive mutant of the deubiquitylase YOD-1 enhances antigen cross-presentation.
去泛素化酶 YOD-1 的催化失活突变体增强抗原交叉呈递。
Blood. 2013 Feb 14;121(7):1145-56. doi: 10.1182/blood-2012-08-447409. Epub 2012 Dec 13.
4
Quantitating protein synthesis, degradation, and endogenous antigen processing.定量蛋白质合成、降解及内源性抗原加工。
Immunity. 2003 Mar;18(3):343-54. doi: 10.1016/s1074-7613(03)00051-7.
5
Efficient presentation of soluble antigen by cultured human dendritic cells is maintained by granulocyte/macrophage colony-stimulating factor plus interleukin 4 and downregulated by tumor necrosis factor alpha.培养的人树突状细胞对可溶性抗原的有效呈递可通过粒细胞/巨噬细胞集落刺激因子加白细胞介素4得以维持,而被肿瘤坏死因子α下调。
J Exp Med. 1994 Apr 1;179(4):1109-18. doi: 10.1084/jem.179.4.1109.
6
Dendritic cells are accessory cells for the development of anti-trinitrophenyl cytotoxic T lymphocytes.树突状细胞是抗三硝基苯细胞毒性T淋巴细胞发育的辅助细胞。
J Exp Med. 1980 Oct 1;152(4):1070-84. doi: 10.1084/jem.152.4.1070.
7
Immunization of dissociated spleen cell cultures from normal mice.对来自正常小鼠的脾细胞解离培养物进行免疫接种。
J Exp Med. 1967 Sep 1;126(3):423-42. doi: 10.1084/jem.126.3.423.
8
Identification of a novel cell type in peripheral lymphoid organs of mice. II. Functional properties in vitro.小鼠外周淋巴器官中一种新型细胞类型的鉴定。II. 体外功能特性
J Exp Med. 1974 Feb 1;139(2):380-97. doi: 10.1084/jem.139.2.380.
9
Identification of a novel cell type in peripheral lymphoid organs of mice. I. Morphology, quantitation, tissue distribution.小鼠外周淋巴器官中一种新型细胞类型的鉴定。I. 形态学、定量分析、组织分布
J Exp Med. 1973 May 1;137(5):1142-62. doi: 10.1084/jem.137.5.1142.