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Cyclosporine A, in Contrast to Rapamycin, Affects the Ability of Dendritic Cells to Induce Immune Tolerance Mechanisms.环孢素 A 与雷帕霉素相反,影响树突状细胞诱导免疫耐受机制的能力。
Arch Immunol Ther Exp (Warsz). 2021 Oct 10;69(1):27. doi: 10.1007/s00005-021-00632-7.
2
Insights Into Dendritic Cells in Cancer Immunotherapy: From Bench to Clinical Applications.癌症免疫治疗中树突状细胞的见解:从实验台到临床应用
Front Cell Dev Biol. 2021 Jun 28;9:686544. doi: 10.3389/fcell.2021.686544. eCollection 2021.
3
Opisthorchis viverrini antigens up-regulates the expression of CD80 and MHC class II in JAWSII mouse dendritic cells and promotes IL-10 and TGF-β secretions.华支睾吸虫抗原上调 JAWSII 小鼠树突状细胞中 CD80 和 MHC Ⅱ类分子的表达,并促进 IL-10 和 TGF-β的分泌。
Parasitol Int. 2021 Oct;84:102401. doi: 10.1016/j.parint.2021.102401. Epub 2021 May 31.
4
Dendritic cell biocompatibility of ether-based urethane films.基于醚的聚氨酯薄膜的树突状细胞生物相容性。
J Appl Toxicol. 2021 Sep;41(9):1456-1466. doi: 10.1002/jat.4136. Epub 2021 Jan 8.
5
Solar inactivated Vibrio cholerae induces maturation of JAWS II dendritic cell line in vitro.经阳光灭活的霍乱弧菌可诱导 JAWS II 树突状细胞系体外成熟。
J Water Health. 2020 Aug;18(4):494-504. doi: 10.2166/wh.2020.040.
6
Efficient Doxorubicin Loading to Isolated Dexosomes of Immature JAWSII Cells: Formulated and Characterized as the Bionanomaterial.阿霉素高效负载至未成熟JAWSII细胞的分离外泌体:制备并表征为生物纳米材料
Materials (Basel). 2020 Jul 27;13(15):3344. doi: 10.3390/ma13153344.
7
Dendritic Cells in Anticancer Vaccination: Rationale for Ex Vivo Loading or In Vivo Targeting.抗癌疫苗接种中的树突状细胞:体外负载或体内靶向的原理
Cancers (Basel). 2020 Mar 5;12(3):590. doi: 10.3390/cancers12030590.
8
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9
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PI3K activity in dendritic cells exerts paradoxical effects during autoimmune inflammation.树突状细胞中的 PI3K 活性在自身免疫性炎症中发挥矛盾的作用。
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贴壁和非贴壁JAWS II树突状细胞的异质性。

Heterogeneity of adherent and non‑adherent JAWS II dendritic cells.

作者信息

Maruszewska-Cheruiyot Marta, Machcińska Maja, Kierasińska Magdalena, Donskow-Lysoniewska Katarzyna

机构信息

Department of Experimental Immunotherapy, Faculty of Medicine, Lazarski University, 02-662 Warsaw, Poland.

Laboratory of Parasitology, General Karol Kaczkowski Military Institute of Hygiene and Epidemiology, 01-163 Warsaw, Poland.

出版信息

Oncol Lett. 2023 Jan 25;25(3):93. doi: 10.3892/ol.2023.13680. eCollection 2023 Mar.

DOI:10.3892/ol.2023.13680
PMID:36817038
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9932576/
Abstract

Dendritic cells (DCs) are crucial in the development of immune responses. DC JAWS II is a murine cell line frequently used in DC studies. These cells are grown in two cell fractions: Adherent and non-adherent. The present study aimed to compare these two fractions in both immature and lipopolysaccharide (LPS)-activated JAWS II cells. The present study analysed the condition, phenotype, antigen uptake capability, signalling properties and the influence on the activity of T cells using flow cytometry, mixed cell reaction and ELISA methods. Adherent immature JAWS II cells exhibited increased endocytosis and decreased activation of the Pi3K signalling pathway. After LPS activation, adherent JAWS II cells exhibited increased expression levels of CD80 and CD86 costimulatory molecules, increased endocytosis and an elevated ability to induce T cell proliferation, compared with non-adherent cells. These results demonstrated that the two fractions of JAWS II adherent and non-adherent cells exhibited different properties and this should be taken into account in the planning of research.

摘要

树突状细胞(DCs)在免疫反应的发展中至关重要。DC JAWS II是一种常用于DC研究的小鼠细胞系。这些细胞以两种细胞组分生长:贴壁细胞和非贴壁细胞。本研究旨在比较未成熟和脂多糖(LPS)激活的JAWS II细胞中的这两种组分。本研究使用流式细胞术、混合细胞反应和ELISA方法分析了细胞状态、表型、抗原摄取能力、信号特性以及对T细胞活性的影响。贴壁未成熟JAWS II细胞表现出内吞作用增加以及Pi3K信号通路激活减少。LPS激活后,与非贴壁细胞相比,贴壁JAWS II细胞表现出共刺激分子CD80和CD86表达水平增加、内吞作用增加以及诱导T细胞增殖的能力增强。这些结果表明,JAWS II贴壁细胞和非贴壁细胞的两种组分表现出不同的特性,在研究规划中应考虑到这一点。