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体液免疫刺激。IV. 补体的作用。

Humoral immunostimulation. IV. Role of complement.

作者信息

Shearer W T, Atkinson J P, Frank M M, Parker C W

出版信息

J Exp Med. 1975 Apr 1;141(4):736-52.

Abstract

When L cells were treated with anti-L-cell antibody in medium containing heat-inactivated fetal calf serum, nucleoside uptake and cell growth were stimulated. The response was markedly increased when fresh, unheated sera from calves, guinea pigs, humans, mice, or rabbits were also present. The factors in unheated serum responsible for the enhancement of immunostimulation were studied. Using low concentrations of sera deficient in various complement (C) components and low concentrations of antibody no augmentation of immunostimulation was seen with Clr-deficient human serum, C2-deficient human serum, C2,4-deficient human serum, C4-deficient guinea pig serum, C3-C9-depleted guinea pig serum (by administration of cobra venom factor to animals), but stimulation was observed with C5-deficient human serum, C5-deficient mouse serum, and C6-deficient rabbit serum. When the concentration of anti-serum was raised, however, augmentation was observed with C4-deficient guinea pig serum. Thus, at low concentrations of antiserum enhancement appeared to occur through the classical C pathway, whereas at high concentrations of antibody either the classical or alternate C pathways appeared to be involved. Stimulation was specifically restored by purified C2 in C2-deficient serum and by C3 in C3-C9-deficient serum. Under the usual reaction conditions consumption of guinea pig C component C4 could be demonstrated which provided direct evidence for activation of the classical C pathway under conditions leading to immunostimulation. By immunofluorescence, cells treated with antibody and normal human serum had human C3 deposited at the cell surface. Taken together these observations suggest that C activated through C3 by either the classical or alternate pathways has the potential to enhance nucleoside incorporation into DNA and cell growth of cells exposed to limiting amounts of antibody. Although the mechanism of stimulation is unknown, it is likely to involve a direct effect of C3 at the level of the cell membrane.

摘要

当L细胞在含有热灭活胎牛血清的培养基中用抗L细胞抗体处理时,核苷摄取和细胞生长受到刺激。当同时存在来自小牛、豚鼠、人类、小鼠或兔子的新鲜、未加热血清时,反应明显增强。对未加热血清中负责增强免疫刺激的因子进行了研究。使用低浓度缺乏各种补体(C)成分的血清和低浓度抗体时,在缺乏Clr的人血清、缺乏C2的人血清、缺乏C2,4的人血清、缺乏C4的豚鼠血清、C3 - C9耗尽的豚鼠血清(通过给动物注射眼镜蛇毒因子)中未观察到免疫刺激增强,但在缺乏C5的人血清、缺乏C5的小鼠血清和缺乏C6的兔子血清中观察到刺激。然而,当抗血清浓度升高时,在缺乏C4的豚鼠血清中观察到增强。因此,在低浓度抗血清时,增强似乎通过经典C途径发生,而在高浓度抗体时,经典或替代C途径似乎都参与其中。在缺乏C2的血清中,纯化的C2特异性恢复刺激,在缺乏C3 - C9的血清中,C3特异性恢复刺激。在通常的反应条件下,可以证明豚鼠C成分C4的消耗,这为在导致免疫刺激的条件下经典C途径的激活提供了直接证据。通过免疫荧光,用抗体和正常人血清处理的细胞在细胞表面沉积有人C3。这些观察结果综合起来表明,通过经典或替代途径通过C3激活的C有潜力增强核苷掺入暴露于限量抗体的细胞的DNA中以及细胞生长。虽然刺激机制尚不清楚,但可能涉及C3在细胞膜水平的直接作用。

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