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腹水超滤液对艾氏腹水癌细胞体外增殖的类抑素样抑制作用。

Chalone-like inhibition of Ehrlich ascites cell proliferation in vitro by an ultrafiltrate obtained from the ascitic fluid.

作者信息

Lehmann W, Graetz H, Schütt M, Langen P

出版信息

Acta Biol Med Ger. 1977;36(7-8):K 43-52.

PMID:148196
Abstract

An aqueous ultrafiltrate (10 000-50 000 dalton) prepared from the cell-free ascitic fluid of mice bearing Ehrlich ascites tumour (EAT) in the plateau phase of growth (12-16 days after transplantation) was investigated with regard to its inhibitory effects on the proliferation of EAT cells in a 24-hr suspension culture. The following results were obtained: (1) The in vitro proliferation of cells obtained from the plateau phase of in vivo growth was reversibly inhibited. (2) The dose-response curves show a plateau with a maximum inhibition of about 50%, which suggests that not all cells can be affected. (3) Young cells (4-6 days after transplantation) were not inhibited. (4) Preincubation of plateau phase cells in the culture medium before treatment abolishes the inhibitory effect of the ultrafiltrate. This effect of preincubation is dependent on time and serum concentration. It provides the possibility to differentiate between true "chalone-like" and cytotoxic effects. (5) the inhibitory properties of the ultrafiltrate are destroyed by heating or trypsin treatment. (6) Extracts prepared in the same way from ascitic fluid of mice bearing lymphocytic leukemia L1210 do not inhibit the proliferation of EAT cells. Corresponding extracts from ascitic fluid of mice bearing myelocytic leukemia YM were found to be inhibitory; however, the inhibitory effect was also found on preincubated cells and is therefore considered to be due to an unspecific cytotoxicity. In conclusion, evidence was obtained for a factor from the ascitic fluid of mice bearing EAT, which prevents EAT cells from entering the proliferating state.

摘要

对处于生长平台期(移植后12 - 16天)的荷艾氏腹水瘤(EAT)小鼠的无细胞腹水制备的水相超滤物(10000 - 50000道尔顿),在24小时悬浮培养中对EAT细胞增殖的抑制作用进行了研究。得到以下结果:(1)从体内生长平台期获得的细胞的体外增殖受到可逆性抑制。(2)剂量反应曲线显示有一个平台期,最大抑制率约为50%,这表明并非所有细胞都会受到影响。(3)年轻细胞(移植后4 - 6天)未受抑制。(4)在处理前将平台期细胞在培养基中预孵育可消除超滤物的抑制作用。这种预孵育的效果取决于时间和血清浓度。它提供了区分真正的“类抑素”效应和细胞毒性效应的可能性。(5)超滤物的抑制特性可通过加热或胰蛋白酶处理而被破坏。(6)从荷淋巴细胞白血病L1210小鼠的腹水中以相同方式制备的提取物不抑制EAT细胞的增殖。发现从荷髓细胞白血病YM小鼠的腹水中得到的相应提取物具有抑制作用;然而,在预孵育细胞上也发现了这种抑制作用,因此被认为是由于非特异性细胞毒性所致。总之,已获得证据表明来自荷EAT小鼠腹水的一种因子可阻止EAT细胞进入增殖状态。

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