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限制素:一种优先影响B淋巴细胞前体的类干扰素细胞因子。

Limitin: An interferon-like cytokine that preferentially influences B-lymphocyte precursors.

作者信息

Oritani K, Medina K L, Tomiyama Y, Ishikawa J, Okajima Y, Ogawa M, Yokota T, Aoyama K, Takahashi I, Kincade P W, Matsuzawa Y

机构信息

Department of Internal Medicine and Molecular Science, Graduate School of Medicine, Osaka University, 2-2 Yamada-oka, Suita City, Osaka 565-0871, Japan.

出版信息

Nat Med. 2000 Jun;6(6):659-66. doi: 10.1038/76233.

DOI:10.1038/76233
PMID:10835682
Abstract

We have identified an interferon-like cytokine, limitin, on the basis of its ability to arrest the growth of or kill lympho-hematopoietic cells. Limitin strongly inhibited B lymphopoiesis in vitro and in vivo but had little influence on either myelopoiesis or erythropoiesis. Because limitin uses the interferon alpha/beta receptors and induces interferon regulatory factor-1, it may represent a previously unknown type I interferon prototype. However, preferential B-lineage growth inhibition and activation of Janus kinase 2 in a myelomonocytic leukemia line have not been described for previously known interferons.

摘要

我们基于其阻止淋巴造血细胞生长或杀伤淋巴造血细胞的能力,鉴定出一种类干扰素细胞因子——限制素。限制素在体外和体内均强烈抑制B淋巴细胞生成,但对髓细胞生成或红细胞生成影响甚微。由于限制素利用干扰素α/β受体并诱导干扰素调节因子-1,它可能代表一种此前未知的I型干扰素原型。然而,此前已知的干扰素尚未有过在髓单核细胞白血病系中优先抑制B系生长和激活Janus激酶2的相关描述。

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Limitin: An interferon-like cytokine that preferentially influences B-lymphocyte precursors.限制素:一种优先影响B淋巴细胞前体的类干扰素细胞因子。
Nat Med. 2000 Jun;6(6):659-66. doi: 10.1038/76233.
2
Limitin: an interferon-like cytokine without myeloerythroid suppressive properties.限制素:一种无髓系红细胞抑制特性的类干扰素细胞因子。
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Limitin, an interferon-like cytokine, transduces inhibitory signals on B-cell growth through activation of Tyk2, but not Stat1, followed by induction and nuclear translocation of Daxx.限制素是一种干扰素样细胞因子,它通过激活酪氨酸激酶2(Tyk2)而非信号转导子和转录激活子1(Stat1),继而诱导死亡结构域相关蛋白(Daxx)并使其发生核转位,从而转导抑制B细胞生长的信号。
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Early type I interferon-mediated signals on B cells specifically enhance antiviral humoral responses.B细胞上早期I型干扰素介导的信号特异性增强抗病毒体液反应。
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Biochemistry. 2004 Oct 5;43(39):12498-512. doi: 10.1021/bi049111r.

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