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巨噬细胞Ia表达调控的功能意义。

Functional significance of the regulation of macrophage Ia expression.

作者信息

Beller D I

出版信息

Eur J Immunol. 1984 Feb;14(2):138-43. doi: 10.1002/eji.1830140207.

Abstract

The relationship of Ia expression and antigen-presenting function by macrophages has been evaluated. When macrophages are maintained in standard culture media, both Ia antigens and accessory cell function are lost. The reacquisition of these properties follows exposure to an Ia-inducing lymphokine, for which cDNA-derived interferon-gamma may substitute. The induction of function is related quantitatively to the level of Ia expression. Moreover, both properties reflect newly expressed Ia determinants, since treatment with anti-I-A plus complement at the beginning of culture diminishes neither the subsequent level of Ia expression nor function. Treatment with anti-Mac-1 plus complement, however, reduces function commensurate with the effectiveness of macrophage depletion. Finally, we find that fixation of macrophages after exposure to antigen does not inhibit antigen presentation, indicating that metabolic activity, while required for antigen processing, is not necessary for presentation.

摘要

巨噬细胞Ia表达与抗原呈递功能之间的关系已得到评估。当巨噬细胞在标准培养基中培养时,Ia抗原和辅助细胞功能都会丧失。接触Ia诱导性淋巴因子后,这些特性会重新获得,cDNA衍生的干扰素-γ可替代该淋巴因子。功能的诱导在数量上与Ia表达水平相关。此外,这两种特性均反映了新表达的Ia决定簇,因为在培养开始时用抗I-A加补体处理既不会降低随后的Ia表达水平,也不会影响功能。然而,用抗Mac-1加补体处理会根据巨噬细胞清除的效果相应降低功能。最后,我们发现抗原接触后巨噬细胞的固定并不抑制抗原呈递,这表明代谢活性虽然是抗原加工所必需的,但不是呈递所必需的。

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