• 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

蛋白聚糖诱导的小鼠关节炎中淋巴细胞向淋巴组织和滑膜组织的迁移与归巢

Migration and homing of lymphocytes to lymphoid and synovial tissues in proteoglycan-induced murine arthritis.

作者信息

Mikecz K, Glant T T

机构信息

Rush Medical College, Rush-Presbyterian-St. Luke's Medical Center, Chicago, Illinois 60612.

出版信息

Arthritis Rheum. 1994 Sep;37(9):1395-403. doi: 10.1002/art.1780370919.

DOI:10.1002/art.1780370919
PMID:7945505
Abstract

OBJECTIVE

To describe the migration and homing of labeled donor lymphocytes to the lymphoid organs and synovial tissues of host animals, during the development of cartilage proteoglycan (PG)-induced arthritis adoptively transferred to syngeneic BALB/c mice.

METHODS

Lymphocytes from either nonarthritic or arthritic donor animals were labeled with either fluorescent or radioactive cell linkers (PKH-GL) and injected into syngeneic, immunosuppressed mice. The homing patterns of donor lymphocytes following the injection of labeled cells were studied by fluorescence microscopy and by measurement of radioactivity in tissue samples.

RESULTS

Lymphocytes from arthritic donors retained their ability to transfer the disease after labeling. In the lymphoid organs, arthritic and nonarthritic donor lymphocytes exhibited similar homing patterns, although remarkable differences were found in the number of homing cells derived from nonarthritic and arthritic donors. However, labeled cells only from arthritic animals migrated to the synovial tissue of the recipient mice, and their appearance was associated with the onset of arthritis.

CONCLUSION

Lymphocytes from mice with PG-induced arthritis, in contrast to lymphocytes from non-arthritic donors, exhibit preferential homing to the synovial tissue of the host. Adoptive transfer of arthritis is linked to the appearance of these cells in the synovium.

摘要

目的

描述在将软骨蛋白聚糖(PG)诱导的关节炎过继转移至同基因BALB/c小鼠的过程中,标记的供体淋巴细胞向宿主动物的淋巴器官和滑膜组织的迁移与归巢情况。

方法

来自非关节炎或关节炎供体动物的淋巴细胞用荧光或放射性细胞连接剂(PKH-GL)标记,然后注射到同基因、免疫抑制的小鼠体内。通过荧光显微镜和测量组织样本中的放射性来研究注射标记细胞后供体淋巴细胞的归巢模式。

结果

来自关节炎供体的淋巴细胞在标记后仍保留其转移疾病的能力。在淋巴器官中,关节炎和非关节炎供体淋巴细胞表现出相似的归巢模式,尽管在源自非关节炎和关节炎供体的归巢细胞数量上发现了显著差异。然而,只有来自关节炎动物的标记细胞迁移到受体小鼠的滑膜组织,并且它们的出现与关节炎的发作相关。

结论

与来自非关节炎供体的淋巴细胞相比,PG诱导的关节炎小鼠的淋巴细胞表现出优先归巢至宿主的滑膜组织。关节炎的过继转移与这些细胞在滑膜中的出现有关。

相似文献

1
Migration and homing of lymphocytes to lymphoid and synovial tissues in proteoglycan-induced murine arthritis.蛋白聚糖诱导的小鼠关节炎中淋巴细胞向淋巴组织和滑膜组织的迁移与归巢
Arthritis Rheum. 1994 Sep;37(9):1395-403. doi: 10.1002/art.1780370919.
2
Proteoglycan-induced polyarthritis and spondylitis adoptively transferred to naive (nonimmunized) BALB/c mice.蛋白聚糖诱导的多关节炎和脊柱炎过继转移至未经免疫的幼稚BALB/c小鼠。
Arthritis Rheum. 1990 Jun;33(6):866-76. doi: 10.1002/art.1780330614.
3
Development of proteoglycan-induced arthritis depends on T cell-supported autoantibody production, but does not involve significant influx of T cells into the joints.蛋白聚糖诱导性关节炎的发展依赖于 T 细胞支持的自身抗体产生,但不涉及 T 细胞大量涌入关节。
Arthritis Res Ther. 2010;12(2):R44. doi: 10.1186/ar2954. Epub 2010 Mar 18.
4
Recruitment of lymphoblasts derived from peripheral and intestinal lymph to synovium and other tissues in normal rats and rats with adjuvant arthritis.正常大鼠和佐剂性关节炎大鼠外周和肠道淋巴来源的淋巴母细胞向滑膜及其他组织的募集
J Immunol. 1996 Dec 1;157(11):5198-207.
5
Temporal changes in the distribution of thoracic duct lymphoblasts to synovium and other tissues of rats with adjuvant-induced arthritis.
Immunol Cell Biol. 2002 Apr;80(2):148-55. doi: 10.1046/j.1440-1711.2002.01054.x.
6
Expression of CD44 and L-selectin in the innate immune system is required for severe joint inflammation in the proteoglycan-induced murine model of rheumatoid arthritis.在蛋白聚糖诱导的类风湿性关节炎小鼠模型中,严重的关节炎症需要先天性免疫系统中CD44和L-选择素的表达。
J Immunol. 2006 Aug 1;177(3):1932-40. doi: 10.4049/jimmunol.177.3.1932.
7
Role of gamma delta T cells in murine collagen-induced arthritis.γδ T细胞在小鼠胶原诱导性关节炎中的作用。
J Immunol. 1993 Dec 1;151(11):6546-58.
8
T and B cell recovery in arthritis adoptively transferred to SCID mice: antigen-specific activation is required for restoration of autopathogenic CD4+ Th1 cells in a syngeneic system.过继转移至重症联合免疫缺陷(SCID)小鼠的关节炎模型中的T和B细胞恢复:在同基因系统中,自身致病性CD4 + Th1细胞的恢复需要抗原特异性激活。
J Immunol. 2002 Jun 15;168(12):6013-21. doi: 10.4049/jimmunol.168.12.6013.
9
In vivo migration of radiolabelled lymphocytes in rheumatoid synovial tissue engrafted in SCID mice: implication of beta 2 and beta 7-integrin.放射性标记淋巴细胞在移植于SCID小鼠体内的类风湿性滑膜组织中的体内迁移:β2和β7整合素的作用
J Rheumatol. 1996 Jan;23(1):32-5.
10
Lymphocyte-independent connective tissue mast cells populate murine synovium.不依赖淋巴细胞的结缔组织肥大细胞存在于小鼠滑膜中。
Arthritis Rheum. 2006 Sep;54(9):2863-71. doi: 10.1002/art.22058.

引用本文的文献

1
Preclinical models of arthritis for studying immunotherapy and immune tolerance.关节炎的临床前模型用于研究免疫疗法和免疫耐受。
Ann Rheum Dis. 2021 Oct;80(10):1268-1277. doi: 10.1136/annrheumdis-2021-220043. Epub 2021 Aug 11.
2
Humanized Mouse Models of Rheumatoid Arthritis for Studies on Immunopathogenesis and Preclinical Testing of Cell-Based Therapies.类风湿关节炎的人源化小鼠模型用于免疫发病机制研究和基于细胞的疗法的临床前测试。
Front Immunol. 2019 Feb 19;10:203. doi: 10.3389/fimmu.2019.00203. eCollection 2019.
3
Proteoglycan aggrecan conducting T cell activation and apoptosis in a murine model of rheumatoid arthritis.
蛋白聚糖聚集蛋白在类风湿关节炎小鼠模型中诱导 T 细胞激活和凋亡。
Biomed Res Int. 2014;2014:942148. doi: 10.1155/2014/942148. Epub 2014 Jan 29.
4
Interferon-γ regulates discordant mechanisms of uveitis versus joint and axial disease in a murine model resembling spondylarthritis.在一个类似脊柱关节炎的小鼠模型中,γ干扰素调节葡萄膜炎与关节及轴性疾病的不同机制。
Arthritis Rheum. 2012 Mar;64(3):762-71. doi: 10.1002/art.33404.
5
Gene expression profiling in murine autoimmune arthritis during the initiation and progression of joint inflammation.小鼠自身免疫性关节炎关节炎症起始和进展过程中的基因表达谱分析。
Arthritis Res Ther. 2005;7(2):R196-207. doi: 10.1186/ar1472. Epub 2004 Dec 14.
6
CD4+CD25+ immunoregulatory T cells may not be involved in controlling autoimmune arthritis.CD4+CD25+免疫调节性T细胞可能不参与控制自身免疫性关节炎。
Arthritis Res Ther. 2003;5(2):R106-13. doi: 10.1186/ar624. Epub 2003 Jan 20.
7
Continuous nasal administration of antigen is critical to maintain tolerance in adoptively transferred autoimmune arthritis in SCID mice.持续经鼻给予抗原对于维持SCID小鼠过继转移的自身免疫性关节炎中的免疫耐受至关重要。
Clin Exp Immunol. 2002 Aug;129(2):224-31. doi: 10.1046/j.1365-2249.2002.01903.x.
8
Aggrecan: A Target Molecule of Autoimmune Reactions.聚集蛋白聚糖:自身免疫反应的靶分子。
Pathol Oncol Res. 1996;2(4):219-228. doi: 10.1007/BF02904814.
9
Antigen-specific B cells present cartilage proteoglycan (aggrecan) to an autoreactive T cell hybridoma derived from a mouse with proteoglycan-induced arthritis.抗原特异性B细胞将软骨蛋白聚糖(聚集蛋白聚糖)呈递给源自患有蛋白聚糖诱导性关节炎小鼠的自身反应性T细胞杂交瘤。
Clin Exp Immunol. 1995 Sep;101(3):414-21. doi: 10.1111/j.1365-2249.1995.tb03128.x.