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识别死亡:凋亡细胞的肝脏吞噬作用。

Recognizing death: liver phagocytosis of apoptotic cells.

作者信息

Dini L

机构信息

Department of Biology, University of Lecce, Italy.

出版信息

Eur J Histochem. 2000;44(3):217-27.

PMID:11095093
Abstract

Apoptosis impacts on nearly all areas of cell biology and continues to draw increasing numbers of investigators to join in the multifaceted race to understand it. Within the study of cell death the area that has less benefited from the fast advances has been the study of the phagocytic process of apoptotic cells. But finally this field is now converging the attention and the studies of an increasing number of researchers that are highlighting its importance. This review deals with removal of apoptotic cells; in particular, the liver cell mediated removal of apoptotic blood cells will be considered. The involvement of carbohydrate-specific receptors of liver cells in the recognition and engulfment of apoptotic cells has been tested using three different experimental approaches: i- in vivo induction of apoptosis; ii- in vitro phagocytosis; iii- in situ adhesion experiments. All three main cell liver types are able to recognize and internalize apoptotic cells mainly by means of carbohydrate-specific receptors (galactose and mannose). By up-regulating the cell surface expression of mannose receptors of the endothelial cells, the recognition and the internalization of apoptotic lymphocytes can be increased. Of note is the discrimination in the recognition of apoptotic lymphocytes by the sinusoidal cells: only homologous cells are rapidly and efficiently deleted from the circulation.

摘要

细胞凋亡影响着细胞生物学的几乎所有领域,并且持续吸引越来越多的研究人员参与到这场旨在了解它的多方面竞争中来。在细胞死亡的研究中,从快速进展中受益较少的领域是凋亡细胞吞噬过程的研究。但最终,这个领域现在正汇聚越来越多研究人员的关注和研究,他们强调了其重要性。这篇综述论述了凋亡细胞的清除;特别是,将考虑肝细胞介导的凋亡血细胞的清除。已使用三种不同的实验方法测试了肝细胞碳水化合物特异性受体在凋亡细胞识别和吞噬中的作用:i - 体内凋亡诱导;ii - 体外吞噬;iii - 原位黏附实验。所有三种主要的肝细胞类型都能够主要通过碳水化合物特异性受体(半乳糖和甘露糖)识别并内化凋亡细胞。通过上调内皮细胞甘露糖受体的细胞表面表达,可以增加凋亡淋巴细胞的识别和内化。值得注意的是,肝血窦细胞对凋亡淋巴细胞的识别存在差异:只有同源细胞能从循环中被快速且有效地清除。

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Recognizing death: liver phagocytosis of apoptotic cells.识别死亡:凋亡细胞的肝脏吞噬作用。
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引用本文的文献

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Hepatocyte-mediated cytotoxicity and host defense mechanisms in the alcohol-injured liver.酒精损伤肝脏中肝细胞介导的细胞毒性和宿主防御机制。
Hepatol Int. 2014 Sep;8 Suppl 2:432-8. doi: 10.1007/s12072-013-9511-7. Epub 2013 Dec 29.
2
Apoptotic cell-derived ICAM-3 promotes both macrophage chemoattraction to and tethering of apoptotic cells.凋亡细胞来源的细胞间黏附分子-3 促进巨噬细胞向凋亡细胞趋化和黏附。
Cell Death Differ. 2012 Apr;19(4):671-9. doi: 10.1038/cdd.2011.167. Epub 2011 Nov 25.
3
Protective molecules--C-reactive protein (CRP), serum amyloid P (SAP), pentraxin3 (PTX3), mannose-binding lectin (MBL), and apolipoprotein A1 (Apo A1), and their autoantibodies: prevalence and clinical significance in autoimmunity.
保护性分子——C反应蛋白(CRP)、血清淀粉样蛋白P(SAP)、五聚素3(PTX3)、甘露糖结合凝集素(MBL)和载脂蛋白A1(Apo A1)及其自身抗体:自身免疫中的患病率及临床意义
J Clin Immunol. 2005 Nov;25(6):582-91. doi: 10.1007/s10875-005-7828-2.
4
The macrophage and the apoptotic cell: an innate immune interaction viewed simplistically?巨噬细胞与凋亡细胞:一种被简单化看待的固有免疫相互作用?
Immunology. 2004 Sep;113(1):1-14. doi: 10.1111/j.1365-2567.2004.01959.x.
5
C1q and mannose binding lectin engagement of cell surface calreticulin and CD91 initiates macropinocytosis and uptake of apoptotic cells.细胞表面钙网蛋白和CD91的C1q及甘露糖结合凝集素结合启动巨胞饮作用和凋亡细胞摄取。
J Exp Med. 2001 Sep 17;194(6):781-95. doi: 10.1084/jem.194.6.781.
6
Bcl-2-dependent oxidation of pyruvate dehydrogenase-E2, a primary biliary cirrhosis autoantigen, during apoptosis.细胞凋亡过程中,原发性胆汁性肝硬化自身抗原丙酮酸脱氢酶-E2的Bcl-2依赖性氧化作用
J Clin Invest. 2001 Jul;108(2):223-32. doi: 10.1172/JCI10716.