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急性期蛋白与转化细胞。

Acute phase proteins and transformed cells.

作者信息

Mackiewicz A

机构信息

Department of Cancer Immunology, University School of Medical Sciences, GreatPoland Cancer Center, Poznań, Poland.

出版信息

Int Rev Cytol. 1997;170:225-300. doi: 10.1016/s0074-7696(08)61623-x.

DOI:10.1016/s0074-7696(08)61623-x
PMID:9002238
Abstract

Acute phase proteins (APP) are plasma proteins whose concentration and glycosylation alters in response to tissue injury, inflammation, or tumor growth. Significant interspecies and sex differences in APP response exist. APP are produced mainly by hepatocytes, and their synthesis and glycosylation are controlled by a network consisting of cytokines, their soluble receptors, and glucocorticoids. The major cytokines involved in these processes belong to a group of interleukin-6-type cytokines that act through the hematopoietin receptor complex on hepatocytes and JAK-STAT signal transduction pathway. Transformed cells (hepatoma) display significant differences in synthesis of APP, cytokine responsiveness, expression of cytokine-receptor subunits and signal-transduction machinery. The most striking variability relates to the glycosylation alterations induced by cytokines. However, transformed cells (hepatoma) form a basic model for studying and understanding mechanisms controlling the synthesis and glycosylation of APP. Furthermore, APP may be secreted by transformed (tumor) cells of various origins and may display a growth factor-like function in certain cancer types.

摘要

急性期蛋白(APP)是血浆蛋白,其浓度和糖基化会因组织损伤、炎症或肿瘤生长而改变。APP反应存在显著的种间和性别差异。APP主要由肝细胞产生,其合成和糖基化受细胞因子、可溶性受体和糖皮质激素组成的网络控制。参与这些过程的主要细胞因子属于一组白细胞介素-6型细胞因子,它们通过肝细胞上的造血受体复合物和JAK-STAT信号转导途径发挥作用。转化细胞(肝癌细胞)在APP合成、细胞因子反应性、细胞因子受体亚基表达和信号转导机制方面表现出显著差异。最显著的变异性与细胞因子诱导的糖基化改变有关。然而,转化细胞(肝癌细胞)构成了研究和理解控制APP合成和糖基化机制的基本模型。此外,APP可能由各种来源的转化(肿瘤)细胞分泌,并在某些癌症类型中表现出生长因子样功能。

相似文献

1
Acute phase proteins and transformed cells.急性期蛋白与转化细胞。
Int Rev Cytol. 1997;170:225-300. doi: 10.1016/s0074-7696(08)61623-x.
2
Interleukin-6-type cytokine-induced changes in acute phase protein glycosylation.白细胞介素-6型细胞因子诱导的急性期蛋白糖基化变化。
Ann N Y Acad Sci. 1995 Jul 21;762:319-30. doi: 10.1111/j.1749-6632.1995.tb32336.x.
3
[Acute phase blood proteins: role in the homeostasis and their synthesis induction in the liver].
Fiziol Zh (1994). 1994 Jan-Feb;40(1):106-17.
4
[Acute-phase proteins in inflammation].[炎症中的急性期蛋白]
C R Seances Soc Biol Fil. 1995;189(4):563-78.
5
Monokines regulate glycosylation of acute-phase proteins.单核因子调节急性期蛋白的糖基化。
J Exp Med. 1987 Jul 1;166(1):253-8. doi: 10.1084/jem.166.1.253.
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The epidermal growth factor receptor ligand amphiregulin is a negative regulator of hepatic acute-phase gene expression.表皮生长因子受体配体 Amphiregulin 是肝脏急性期基因表达的负调节剂。
J Hepatol. 2009 Dec;51(6):1010-20. doi: 10.1016/j.jhep.2009.06.030. Epub 2009 Sep 12.
7
[Glucocorticoids and acute phase proteins].
J Soc Biol. 1999;193(4-5):375-80.
8
Recombinant oncostatin M stimulates the production of acute phase proteins in HepG2 cells and rat primary hepatocytes in vitro.重组制瘤素M在体外刺激HepG2细胞和大鼠原代肝细胞产生急性期蛋白。
J Immunol. 1992 Mar 15;148(6):1731-6.
9
Cytokines and the hepatic acute-phase response.细胞因子与肝脏急性期反应。
Semin Liver Dis. 1999;19(2):141-55. doi: 10.1055/s-2007-1007106.
10
Leukemia inhibitory factor, interferon gamma and dexamethasone regulate N-glycosylation of alpha 1-protease inhibitor in human hepatoma cells.白血病抑制因子、干扰素γ和地塞米松调节人肝癌细胞中α1-抗胰蛋白酶的N-糖基化。
Eur J Cell Biol. 1993 Apr;60(2):331-6.

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