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活化的巨噬细胞可区分未分化的致瘤性与分化的非致瘤性小鼠红白血病细胞。

Activated macrophages distinguish undifferentiated-tumorigenic from differentiated-nontumorigenic murine erythroleukemia cells.

作者信息

Pak C C, Fidler I J

机构信息

Department of Cell Biology, University of Texas, M.D. Anderson Cancer Center, Houston 77030.

出版信息

Differentiation. 1989 Jul;41(1):49-55. doi: 10.1111/j.1432-0436.1989.tb00731.x.

Abstract

The interaction between macrophages and differentiating cells was examined using murine erythroleukemia cells (MELC). Inflammatory macrophages activated with recombinant murine interferon-gamma (rMuIFN-gamma) and lipopolysaccharide (LPS) first specifically recognized and bound tumorigenic-undifferentiated MELC and then produced their lysis. MELC that were induced to differentiate by a 5-day treatment with 5 mM N,N'-hexamethylene-bis-acetamide (HMBA) accumulated hemoglobin (benzidine positive) and were not recognized by the macrophages. Qualitative examination by light and electron microscopy confirmed the specific nature of the macrophage-MELC interaction. Quantitative assessment showed that the binding was dependent on the temperature and divalent cations and independent of serum components. A 24-h treatment of MELC with HMBA resulted in decreased binding, prior to hemoglobin accumulation and commitment to differentiation. The lack of binding of nontumorigenic-differentiated cells by macrophages was not due to residual HMBA. It thus appears that macrophages can distinguish MELC at different stages of differentiation.

摘要

利用小鼠红白血病细胞(MELC)研究了巨噬细胞与分化细胞之间的相互作用。用重组小鼠干扰素 -γ(rMuIFN -γ)和脂多糖(LPS)激活的炎性巨噬细胞首先特异性识别并结合致瘤性未分化的MELC,然后使其裂解。经5 mM N,N'-六亚甲基双乙酰胺(HMBA)处理5天诱导分化的MELC积累了血红蛋白(联苯胺阳性),未被巨噬细胞识别。光镜和电镜的定性检查证实了巨噬细胞与MELC相互作用的特异性。定量评估表明,结合依赖于温度和二价阳离子,且与血清成分无关。在血红蛋白积累和开始分化之前,用HMBA对MELC进行24小时处理导致结合减少。巨噬细胞对非致瘤性分化细胞缺乏结合并非由于残留的HMBA。因此,巨噬细胞似乎能够区分处于不同分化阶段的MELC。

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