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淋巴细胞表面受体的可逆性丧失。

Reversible loss of surface receptors on lymphocytes.

作者信息

Milton J D, Mowbray J F

出版信息

Immunology. 1972 Oct;23(4):599-608.

Abstract

An α-2-glycoprotein from bovine serum (Fraction C) with immunosuppressive properties and anti-proliferative activity has been shown to reversibly inhibit the synthesis of cell surface receptors . The proliferative response of human lymphocytes to PHA and PPD can be inhibited by prolonged preincubation with Fraction C, which also inhibits the ability of lymphoid cells to bind PHA, 3–4 days for 90 per cent inhibition, and anti-immunoglobulin, 10 hours for 90 per cent inhibition. This inhibition is reversible and the binding ability recovers after removal of Fraction C at a similar rate to that at which it declined. Fraction C also rapidly and reversibly inhibits the secretion of antibody by immune spleen cells . The anti-proliferative effect of Fraction C is shown to involve an effect on ribosomal RNA synthesis and it is suggested that the mechanism of this action depends on the inhibition of protein synthesis, probably mediated by an effect on newly synthesized messenger RNA. The demonstration of different turnover rates of cell surface components on different types of cells suggests that it may be possible to use Fraction C to affect responsiveness of one type of lymphocyte while leaving another type unaffected.

摘要

一种来自牛血清的具有免疫抑制特性和抗增殖活性的α-2-糖蛋白(C组分)已被证明可可逆地抑制细胞表面受体的合成。通过与C组分长时间预孵育,可抑制人淋巴细胞对PHA和PPD的增殖反应,C组分还可抑制淋巴细胞结合PHA的能力,90%抑制率需3 - 4天,抑制抗免疫球蛋白则需10小时达到90%抑制率。这种抑制是可逆的,去除C组分后,结合能力以与下降速率相似的速度恢复。C组分还能快速且可逆地抑制免疫脾细胞分泌抗体。C组分的抗增殖作用显示涉及对核糖体RNA合成的影响,有人提出这种作用机制可能依赖于对蛋白质合成的抑制,可能是通过对新合成的信使RNA的作用介导的。不同类型细胞上细胞表面成分的更新率不同,这表明有可能利用C组分影响一种淋巴细胞的反应性,而使另一种类型的淋巴细胞不受影响。

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