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肿瘤坏死因子-α在体外双向调节原始小鼠造血祖细胞的活力。

TNF-alpha bidirectionally modulates the viability of primitive murine hematopoietic progenitor cells in vitro.

作者信息

Jacobsen F W, Veiby O P, Stokke T, Jacobsen S E

机构信息

Department of Immunology, Institute for Cancer Research, The Norwegian Radium Hospital, Oslo, Norway.

出版信息

J Immunol. 1996 Aug 1;157(3):1193-9.

PMID:8757625
Abstract

It is well established that TNF-alpha can induce apoptosis in many normal and transformed cell types. The effects of TNF-alpha on cytokine-induced proliferation and differentiation of normal hematopoietic progenitors have been characterized extensively, whereas little is known about how TNF-alpha can affect their viability. The present studies suggest, based on experiments using delayed addition of growth-promoting cytokines as well direct viability assays, that TNF-alpha bidirectionally affects the survival of individually cultured primitive Lin- Sca-1+ hematopoietic progenitors, in that stem cell factor (SCF)-, granulocyte-CSF-, IL-6-, and IL-11-induced survival is potently counteracted by TNF-alpha (42-86%), whereas TNF-alpha synergistically enhances IL-1alpha-induced survival up to threefold. The bidirectional effects of TNF-alpha on hematopoietic growth factor-induced survival of hematopoietic progenitors were reflected in that TNF-alpha enhanced apoptosis of Lin- Sca-1+ cells when combined with SCF, whereas TNF-alpha synergistically suppressed apoptosis in response to IL-1alpha.

摘要

肿瘤坏死因子-α(TNF-α)可诱导多种正常细胞和转化细胞发生凋亡,这一点已得到充分证实。TNF-α对细胞因子诱导的正常造血祖细胞增殖和分化的影响已得到广泛研究,然而,关于TNF-α如何影响其生存能力却知之甚少。基于使用延迟添加生长促进细胞因子以及直接生存能力检测的实验,目前的研究表明,TNF-α双向影响单独培养的原始Lin-Sca-1+造血祖细胞的存活,即干细胞因子(SCF)、粒细胞集落刺激因子(G-CSF)、白细胞介素-6(IL-6)和白细胞介素-11(IL-11)诱导的存活被TNF-α有效抵消(42%-86%),而TNF-α协同增强IL-1α诱导的存活高达三倍。TNF-α对造血生长因子诱导的造血祖细胞存活的双向影响体现在,当与SCF联合时,TNF-α增强Lin-Sca-1+细胞的凋亡,而TNF-α协同抑制对IL-1α的凋亡反应。

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