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炎症性贫血的动物模型

Animal models of anemia of inflammation.

作者信息

Rivera Seth, Ganz Tomas

机构信息

Department of Medicine, David Geffen School of Medicine at the University of California, Los Angeles, CA.

出版信息

Semin Hematol. 2009 Oct;46(4):351-7. doi: 10.1053/j.seminhematol.2009.06.003.

DOI:10.1053/j.seminhematol.2009.06.003
PMID:19786203
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2755601/
Abstract

Anemia of inflammation (AI) is a complex multi-organ response to inflammatory disorders. Because AI can result from many infectious and non-infectious inflammatory diseases, multiple mechanisms may contribute to its pathogenesis, including iron restriction, direct erythropoietic suppression, shortened red blood cell survival, and frank hemolysis. Animal models have been helpful in the study of the mechanisms of AI and its potential treatments, but each model reflects distinct aspects of this heterogeneous syndrome. It is therefore important to study a variety of models of AI. This review focuses on the use of infectious and noninfectious mouse models of inflammation that have been shown to manifest anemia. We review many of the models reported in the literature or developed in our laboratory, and discuss their respective merits and drawbacks.

摘要

炎症性贫血(AI)是对炎症性疾病的一种复杂的多器官反应。由于AI可由多种感染性和非感染性炎症性疾病引起,其发病机制可能涉及多种机制,包括铁限制、直接的红细胞生成抑制、红细胞存活时间缩短以及明显的溶血。动物模型有助于研究AI的发病机制及其潜在治疗方法,但每种模型都反映了这种异质性综合征的不同方面。因此,研究多种AI模型很重要。本综述重点关注已被证明会出现贫血的感染性和非感染性小鼠炎症模型。我们回顾了文献中报道的或我们实验室开发的许多模型,并讨论了它们各自的优缺点。

相似文献

1
Animal models of anemia of inflammation.炎症性贫血的动物模型
Semin Hematol. 2009 Oct;46(4):351-7. doi: 10.1053/j.seminhematol.2009.06.003.
2
Iron sequestration and anemia of inflammation.铁螯合与炎症性贫血
Semin Hematol. 2009 Oct;46(4):387-93. doi: 10.1053/j.seminhematol.2009.06.001.
3
Antihepcidin antibody treatment modulates iron metabolism and is effective in a mouse model of inflammation-induced anemia.抗hepcidin 抗体治疗可调节铁代谢,在炎症性贫血的小鼠模型中有效。
Blood. 2010 Apr 29;115(17):3616-24. doi: 10.1182/blood-2009-09-245977. Epub 2010 Jan 6.
4
The anemia of inflammation/malignancy: mechanisms and management.炎症/恶性肿瘤相关性贫血:机制与管理
Hematology Am Soc Hematol Educ Program. 2008:159-65. doi: 10.1182/asheducation-2008.1.159.
5
[Anemia during inflammatory processes: pathogenesis and clinical and morphological manifestations].[炎症过程中的贫血:发病机制及临床和形态学表现]
Arkh Patol. 2010 Mar-Apr;72(2):56-61.
6
The anemia of inflammation.炎症性贫血
J Clin Rheumatol. 2012 Dec;18(8):437-42. doi: 10.1097/RHU.0b013e318278f553.
7
The microcytic red cell and the anemia of inflammation.小细胞性红细胞与炎症性贫血。
N Engl J Med. 2009 Nov 5;361(19):1904-6. doi: 10.1056/NEJMcibr0906391.
8
Anemia of inflammation: the cytokine-hepcidin link.炎症性贫血:细胞因子与铁调素的联系。
J Clin Invest. 2004 May;113(9):1251-3. doi: 10.1172/JCI21441.
9
Hepcidin antimicrobial peptide transgenic mice exhibit features of the anemia of inflammation.铁调素抗菌肽转基因小鼠表现出炎症性贫血的特征。
Blood. 2007 May 1;109(9):4038-44. doi: 10.1182/blood-2006-10-051755. Epub 2007 Jan 11.
10
Hepcidin in iron metabolism.铁代谢中的铁调素
Curr Opin Hematol. 2004 Jul;11(4):251-4. doi: 10.1097/00062752-200407000-00004.

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本文引用的文献

1
Regulation of iron homeostasis in anemia of chronic disease and iron deficiency anemia: diagnostic and therapeutic implications.慢性病贫血和缺铁性贫血中铁稳态的调节:诊断和治疗意义
Blood. 2009 May 21;113(21):5277-86. doi: 10.1182/blood-2008-12-195651. Epub 2009 Mar 17.
2
Genetic and functional characterization of the mouse Trl3 locus in defense against tuberculosis.小鼠Trl3基因座在抗结核防御中的遗传与功能特性研究
J Immunol. 2009 Mar 15;182(6):3757-67. doi: 10.4049/jimmunol.0802094.
3
STAT6-mediated suppression of erythropoiesis in an experimental model of malarial anemia.
慢性炎症性贫血动物模型中铁调素水平的变化:与铁补充和铁调素调节相关的机制见解。
Oxid Med Cell Longev. 2021 Nov 27;2021:4357756. doi: 10.1155/2021/4357756. eCollection 2021.
4
Ironing out an approach to alleviate the hypoferremia of acute inflammation.摸索出一种缓解急性炎症性低铁血症的方法。
Haematologica. 2021 Feb 1;106(2):326-328. doi: 10.3324/haematol.2020.266627.
5
Bacterial Lipopolysaccharides Suppress Erythroblastic Islands and Erythropoiesis in the Bone Marrow in an Extrinsic and G- CSF-, IL-1-, and TNF-Independent Manner.细菌脂多糖以非 G-CSF、IL-1 和 TNF 依赖的方式抑制骨髓中红系造血岛和红细胞生成。
Front Immunol. 2020 Oct 6;11:583550. doi: 10.3389/fimmu.2020.583550. eCollection 2020.
6
Development of Neutropenic Murine Models of Iron Overload and Depletion To Study the Efficacy of Siderophore-Antibiotic Conjugates.铁过载和耗竭的中性粒细胞减少症小鼠模型的开发,以研究铁载体-抗生素偶联物的疗效。
Antimicrob Agents Chemother. 2019 Dec 20;64(1). doi: 10.1128/AAC.01961-19.
7
Multi-tissue network analysis for drug prioritization in knee osteoarthritis.多组织网络分析在膝骨关节炎药物优先级中的应用。
Sci Rep. 2019 Oct 23;9(1):15176. doi: 10.1038/s41598-019-51627-6.
8
Animal Models of Normal and Disturbed Iron and Copper Metabolism.动物模型的正常和紊乱的铁和铜代谢。
J Nutr. 2019 Dec 1;149(12):2085-2100. doi: 10.1093/jn/nxz172.
9
Tinospora cordifolia protects against inflammation associated anemia by modulating inflammatory cytokines and hepcidin expression in male Wistar rats.三叶鬼针草通过调节雄性 Wistar 大鼠炎性细胞因子和铁调素的表达来防治与炎症相关的贫血。
Sci Rep. 2019 Jul 29;9(1):10969. doi: 10.1038/s41598-019-47458-0.
10
Development of a model for anemia of inflammation that is relevant to critical care.建立一种与重症监护相关的炎症性贫血模型。
Intensive Care Med Exp. 2019 Jul 25;7(Suppl 1):47. doi: 10.1186/s40635-019-0261-2.
STAT6介导的疟疾病理性贫血实验模型中红细胞生成的抑制作用
Haematologica. 2009 Feb;94(2):195-204. doi: 10.3324/haematol.13422. Epub 2008 Dec 23.
4
Assessment of urinary concentrations of hepcidin provides novel insight into disturbances in iron homeostasis during malarial infection.评估尿中铁调素浓度为了解疟疾感染期间铁稳态紊乱提供了新的视角。
J Infect Dis. 2009 Jan 15;199(2):253-62. doi: 10.1086/595790.
5
Secreted antibody is required for immunity to Plasmodium berghei.分泌型抗体是对伯氏疟原虫免疫所必需的。
Infect Immun. 2009 Jan;77(1):414-8. doi: 10.1128/IAI.00982-08. Epub 2008 Nov 10.
6
Role of iron homeostasis in trypanosomiasis-associated anemia.铁稳态在锥虫病相关性贫血中的作用。
Immunobiology. 2008;213(9-10):823-35. doi: 10.1016/j.imbio.2008.07.023. Epub 2008 Sep 7.
7
Murine models of anaemia of inflammation: extramedullary haematopoiesis represents a species specific difference to human anaemia of inflammation that can be eliminated by splenectomy.炎症性贫血的小鼠模型:髓外造血代表了与人类炎症性贫血的种属特异性差异,脾切除术可消除这种差异。
Int J Immunopathol Pharmacol. 2008 Jul-Sep;21(3):577-84. doi: 10.1177/039463200802100310.
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Experimental models of sepsis and their clinical relevance.脓毒症的实验模型及其临床相关性。
Shock. 2008 Oct;30 Suppl 1:53-9. doi: 10.1097/SHK.0b013e318181a343.
9
Effect of peptidoglycans on erythrocyte survival.肽聚糖对红细胞存活的影响。
Int J Med Microbiol. 2009 Jan;299(1):75-85. doi: 10.1016/j.ijmm.2008.05.012. Epub 2008 Jul 26.
10
Phlebotomies or erythropoietin injections allow mobilization of iron stores in a mouse model mimicking intensive care anemia.在模拟重症监护贫血的小鼠模型中,放血或注射促红细胞生成素可促使铁储备动员。
Crit Care Med. 2008 Aug;36(8):2388-94. doi: 10.1097/CCM.0b013e31818103b9.