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巨噬细胞炎性蛋白-1α和转化生长因子β对造血祖细胞/干细胞生长的不同及重叠直接作用

Distinct and overlapping direct effects of macrophage inflammatory protein-1 alpha and transforming growth factor beta on hematopoietic progenitor/stem cell growth.

作者信息

Keller J R, Bartelmez S H, Sitnicka E, Ruscetti F W, Ortiz M, Gooya J M, Jacobsen S E

机构信息

Biological Carcinogenesis and Development Program, Program Resources, Inc/DynCorp, National Cancer Institute (NCI)-Frederick Cancer Research and Development Center, MD 21702-1201.

出版信息

Blood. 1994 Oct 1;84(7):2175-81.

PMID:7919333
Abstract

Both transforming growth factor beta (TGF beta) and macrophage inflammatory protein 1 alpha (MIP-1 alpha) have been shown to be multifunctional regulators of hematopoiesis that can either inhibit or enhance the growth of hematopoietic progenitor cells (HPC). We report here the spectrum of activities of these two cytokines on different hematopoietic progenitor and stem cell populations, and whether these effects are direct or indirect. MIP-1 alpha enhances interleukin-3 (IL-3)/and granulocyte-macrophage colony-stimulating factor (GM-CSF)/induced colony formation of normal bone marrow progenitor cells (BMC) and lineage-negative (Lin-) progenitors, but has no effect on G-CSF or CSF-1/induced colony formation. Similarly, TGF beta enhances GM-CSF/induced colony formation of normal BMC and Lin- progenitors. In contrast, TGF beta inhibits IL-3/ and CSF-1/induced colony formation of Lin- progenitors. The effects of MIP-1 alpha and TGF beta on the growth of Lin- progenitors were direct and correlate with colony formation in soft agar. Separation of the Lin- cells into Thy-1 and Thy-1lo subsets showed that the growth of Thy-1lo Lin- cells is directly inhibited by MIP-1 alpha and TGF beta regardless of the cytokine used to stimulate growth (IL-3), GM-CSF, or CSF-1). In contrast, two other stem cell populations (0% to 15% Höechst 33342/Rhodamine 123 [Hö/Rh123] and Lin-Sca-1+ cells) were markedly inhibited by TGF beta and unaffected by MIP-1 alpha. Furthermore, MIP-1 alpha has no effect on high proliferative potential colony-forming cells 1 or 2 (HPP-CFC/1 or /2) colony formation in vitro, whereas TGF beta inhibits both HPP-CFC/1 and HPP-CFC/2. Thus, MIP-1 alpha and TGF beta are direct bidirectional regulators of HPC growth, whose effects are dependent on other growth factors present as well as the maturational state of the HPC assayed. The spectrum of their inhibitory and enhancing activities shows overlapping yet distinct effects.

摘要

转化生长因子β(TGFβ)和巨噬细胞炎性蛋白1α(MIP-1α)均已被证明是造血的多功能调节因子,它们既可以抑制也可以增强造血祖细胞(HPC)的生长。我们在此报告这两种细胞因子对不同造血祖细胞和干细胞群体的活性谱,以及这些作用是直接的还是间接的。MIP-1α增强白细胞介素-3(IL-3)/和粒细胞-巨噬细胞集落刺激因子(GM-CSF)/诱导的正常骨髓祖细胞(BMC)和谱系阴性(Lin-)祖细胞的集落形成,但对G-CSF或CSF-1/诱导的集落形成没有影响。同样,TGFβ增强GM-CSF/诱导的正常BMC和Lin-祖细胞的集落形成。相反,TGFβ抑制IL-3/和CSF-1/诱导的Lin-祖细胞的集落形成。MIP-1α和TGFβ对Lin-祖细胞生长的作用是直接的,并且与软琼脂中的集落形成相关。将Lin-细胞分离为Thy-1和Thy-1lo亚群表明,无论用于刺激生长的细胞因子(IL-3、GM-CSF或CSF-1)如何,Thy-1lo Lin-细胞的生长都受到MIP-1α和TGFβ的直接抑制。相反,另外两个干细胞群体(0%至15%的Hoechst 33342/罗丹明123 [Hö/Rh123]和Lin-Sca-1+细胞)受到TGFβ的显著抑制,而不受MIP-1α的影响。此外,MIP-1α对体外高增殖潜能集落形成细胞1或2(HPP-CFC/1或/2)的集落形成没有影响,而TGFβ抑制HPP-CFC/1和HPP-CFC/2。因此,MIP-1α和TGFβ是HPC生长的直接双向调节因子,其作用取决于存在的其他生长因子以及所检测的HPC的成熟状态。它们的抑制和增强活性谱显示出重叠但又不同的作用。

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