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白细胞补体:C5在淋巴细胞刺激中的可能作用。

Leukocyte complement: a possible role for C5 in lymphocyte stimulation.

作者信息

Sundsmo J S

出版信息

J Immunol. 1983 Aug;131(2):886-91.

PMID:6223096
Abstract

The results presented here show that Fab' antibody fragments directed to complement proteins C5, C6, and C7 inhibit lymphocyte stimulation in mixed lymphocyte culture (MLC) by up to 65%, as determined by decreased incorporation of 3H-thymidine. Lymphocyte stimulation induced by PHA-mitogen was also inhibited up to 100% by anti-C5 Fab'. Specificity of these reactions was established by the findings that goat anti-C5 or murine hybridoma anti-C5 both inhibited MLC; the inhibitory activity of anti-C5 Fab' was absorbed with highly purified C5 (but not with C3), and antibody directed to C3 did not inhibit lymphocyte stimulation by MLC or PHA. The effects of anti-C5 were exerted in a nontoxic manner. Cleavage of lymphocyte associated C5 with factor B (Bb) or with trypsin resulted in stimulation of lymphocyte thymidine incorporation. Purified C5a was found to induce lymphocyte stimulation in serum-free medium in pulse-chase types of experiments. Anti-C6 and C7 Fab' also inhibited lymphocyte stimulation induced in one-way MLC. These results suggest that C5, C5a, and/or C6 and C7 may play a role in triggering of lymphocyte blastogenesis.

摘要

此处呈现的结果表明,针对补体蛋白C5、C6和C7的Fab'抗体片段在混合淋巴细胞培养(MLC)中可将淋巴细胞刺激抑制高达65%,这是通过3H-胸腺嘧啶核苷掺入量的减少来确定的。抗C5 Fab'对PHA-丝裂原诱导的淋巴细胞刺激也可抑制高达100%。这些反应的特异性通过以下发现得以确立:山羊抗C5或鼠杂交瘤抗C5均能抑制MLC;抗C5 Fab'的抑制活性可被高度纯化的C5(而非C3)吸收,且针对C3的抗体不会抑制MLC或PHA诱导的淋巴细胞刺激。抗C5的作用以无毒方式发挥。用B因子(Bb)或胰蛋白酶切割淋巴细胞相关的C5会导致淋巴细胞胸腺嘧啶核苷掺入增加。在脉冲追踪类型的实验中发现,纯化的C5a可在无血清培养基中诱导淋巴细胞刺激。抗C6和C7 Fab'也抑制单向MLC中诱导的淋巴细胞刺激。这些结果表明,C5、C5a和/或C6及C7可能在触发淋巴细胞增殖方面发挥作用。

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