• 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

在新西兰黑鼠(NZB)及其(NZB/NZW)F1杂交鼠发育过程中自身免疫性溶血性贫血时红细胞变形性的变化。

Erythrocyte deformability changes in autoimmune hemolytic anemia during development of NZB mice and their (NZB/NZW)F1 hybrid.

作者信息

Ballas S K, Tabbara K F, Murphy D L, Mohandas N, Clark M R, Shohet S B

出版信息

J Clin Lab Immunol. 1985 Apr;16(4):217-22.

PMID:4020852
Abstract

NZB and B/W hybrid mice develop compensated hemolytic anemia during the first year of their life. By the age of 3-5 months, their erythrocytes show evidence of spherocytosis, increased osmotic fragility and decreased whole cell deformability, as measured by ektacytometry, a laser diffraction technique. The presence of spherocytes with decreased surface area/volume ratio was confirmed by scanning electron microscopy and osmotic gradient ektacytometry. Whereas these abnormalities persisted and worsened in the NZB mice with further growth, they gradually improved and reverted to normal by the age of 12 months in B/W mice. This spontaneous improvement seems to be due to the accumulation of red cell membrane lipids reflecting the lipemia of immune complex nephritis in B/W mice. The implications of these findings in the modulation of autoimmune hemolytic anemia are discussed.

摘要

NZB和B/W杂交小鼠在出生后的第一年发生代偿性溶血性贫血。到3 - 5月龄时,通过激光衍射技术——激光衍射血细胞分析法测量,它们的红细胞呈现出球形红细胞增多、渗透脆性增加和全细胞变形性降低的迹象。通过扫描电子显微镜和渗透梯度激光衍射血细胞分析法证实了表面积/体积比降低的球形红细胞的存在。在NZB小鼠中,随着进一步生长,这些异常持续存在且恶化,而在B/W小鼠中,到12月龄时这些异常逐渐改善并恢复正常。这种自发改善似乎是由于反映B/W小鼠免疫复合物性肾炎脂血症的红细胞膜脂质积累所致。本文讨论了这些发现对自身免疫性溶血性贫血调节的意义。

相似文献

1
Erythrocyte deformability changes in autoimmune hemolytic anemia during development of NZB mice and their (NZB/NZW)F1 hybrid.在新西兰黑鼠(NZB)及其(NZB/NZW)F1杂交鼠发育过程中自身免疫性溶血性贫血时红细胞变形性的变化。
J Clin Lab Immunol. 1985 Apr;16(4):217-22.
2
An animal model to study erythrocyte senescence with a narrow time window of erythrocyte production: alterations in osmotic fragility and deformability of erythrocytes during their life span.一种用于研究红细胞衰老的动物模型,其红细胞生成时间窗狭窄:红细胞寿命期间渗透脆性和变形性的变化。
Clin Hemorheol Microcirc. 1998 Dec;19(4):299-306.
3
Genetic regulation of hypergammaglobulinaemia and the correlation to autoimmune traits in (NZB X NZW) F1 hybrid.(新西兰黑鼠×新西兰白鼠)F1 杂交种中高球蛋白血症的遗传调控及其与自身免疫性状的相关性。
Clin Exp Immunol. 1984 Dec;58(3):694-702.
4
Resting B cells from New Zealand Black mice demonstrate a defect in apoptosis induction following surface IgM ligation.来自新西兰黑鼠的静息B细胞在表面IgM连接后表现出凋亡诱导缺陷。
J Immunol. 1996 Jun 1;156(11):4498-503.
5
Genetic studies of autoimmunity in New Zealand mice. IV. Contribution of NZB and NZW genes to the spontaneous occurrence of retroviral gp70 immune complexes in (NZB X NZW)F1 hybrid and the correlation to renal disease.新西兰小鼠自身免疫的遗传学研究。IV. NZB和NZW基因对(NZB×NZW)F1杂种中逆转录病毒gp70免疫复合物自发出现的贡献及其与肾脏疾病的相关性。
J Immunol. 1983 Feb;130(2):740-6.
6
Male New Zealand Black/KN mice: a novel model for autoimmune-induced permanent alopecia?雄性新西兰黑/ KN小鼠:一种自身免疫性诱导永久性脱发的新模型?
Br J Dermatol. 2006 Aug;155(2):437-45. doi: 10.1111/j.1365-2133.2006.07204.x.
7
Interleukin-6 exacerbates glomerulonephritis in (NZB x NZW)F1 mice.白细胞介素-6会加剧(新西兰黑鼠×新西兰白鼠)F1代小鼠的肾小球肾炎。
Am J Pathol. 1994 May;144(5):927-37.
8
Genes determining autoimmune disease in New Zealand mice.决定新西兰小鼠自身免疫性疾病的基因。
J Clin Lab Immunol. 1981 May;5(3):165-70.
9
[Suppressive action of bone marrow and spleen cells on antibody genesis and lymphoid cell proliferation in an in vitro culture of autoimmune mice (NZB.NZW)F1].[骨髓和脾细胞对自身免疫小鼠(NZB.NZW)F1体外培养中抗体产生和淋巴细胞增殖的抑制作用]
Tsitologiia. 1981 Jul;23(7):834-8.
10
Altered response to and production of TGF-beta by B cells from autoimmune NZB mice.来自自身免疫性新西兰黑鼠(NZB)的B细胞对转化生长因子-β(TGF-β)的反应及产生情况发生改变。
Cell Immunol. 1997 Aug 1;179(2):126-37. doi: 10.1006/cimm.1997.1149.

引用本文的文献

1
Zetomipzomib (KZR-616) attenuates lupus in mice via modulation of innate and adaptive immune responses.泽托米泊佐米(KZR-616)通过调节先天和适应性免疫应答来减轻狼疮小鼠的病情。
Front Immunol. 2023 Mar 10;14:1043680. doi: 10.3389/fimmu.2023.1043680. eCollection 2023.