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Receptors for IgM on human lymphocytes. II. Mitogen-induced modulation of receptor expression.

机译:人淋巴细胞上IgM的受体。二。丝裂原诱导的受体表达调节。

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摘要

Human peripheral lymphocytes undergoing blastogenesis induced by phytohaemagglutinin (PHA) or concanavalin A did not express receptors for the Fc portion of IgM (RFcmu). Furthermore, treatment of lymphocytes with PHA produced a dose-dependent loss of RFcmu which began as early as 5 hr after exposure to the mitogen. Within 24 hr after the addition of PHA, the percentage of lymphocytes expressing RFcmu had decreased from 65% to 4%. Under the same conditions of treatment, the expression of the receptor for sheep erythrocytes (E) was unchanged. These findings seemed inconsistent with a direct blocking effect of PHA but suggested that PHA induced a time-dependent modulation (switch off) of expression of RFcmu. Pronase cleavage of surface proteins on cells incubated with PHA for 24 hr followed by overnight incubation showed an almost complete irreversibility of RFcmu modulation up to 72 hr later. Studies using T cells isolated by E-rosetting showed that RFcmu modulation predominantly occurred on T cells. The modulation of RFcmu expression is discussed in terms of its possible role in the immune response.
机译:植物血凝素(PHA)或伴刀豆球蛋白A诱导的成胚过程的人外周血淋巴细胞不表达IgM(RFcmu)Fc部分的受体。此外,用PHA处理淋巴细胞会产生剂量依赖性的RFcmu损失,这种损失最早在接触有丝分裂原后5小时开始。加入PHA后24小时内,表达RFcmu的淋巴细胞百分比从65%降至4%。在相同的治疗条件下,绵羊红细胞(E)受体的表达未改变。这些发现似乎与PHA的直接阻断作用不一致,但提示PHA诱导了RFcmu表达的时间依赖性调节(关闭)。在与PHA孵育24小时的细胞上进行表面蛋白酶的核酸酶切割,然后过夜孵育,显示直至72小时后,RFcmu调节几乎完全不可逆。使用通过电凝法分离的T细胞的研究表明,RFcmu调节主要发生在T细胞上。根据RFcmu表达在免疫应答中的可能作用来讨论其调控。

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