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携带IgE的淋巴细胞的起源与命运。I. 派尔集合淋巴结作为细胞的分化位点。同时携带IgA和IgE

Origin and fate of IgE-bearing lymphocytes. I. Peyer's patches as differentiation site of cells. Simultaneously bearing IgA and IgE.

作者信息

Durkin H G, Bazin H, Waksman B H

出版信息

J Exp Med. 1981 Sep 1;154(3):640-8. doi: 10.1084/jem.154.3.640.

Abstract

Peyer's patches (PP) from adult conventionally raised (C) and germ-free (GF) rats of the same age differed strikingly in the distributions of cells bearing membrane-bound immunoglobulin of the different isotypes. High concentrations of cells with membrane-bound IgE (approximately 20% of total cells determined by indirect immunofluorescence) were found in PP of rats, whereas IgE+ cells were absent from PP of C rats. The numbers of IgA+ cells were almost threefold higher in PP of GF rats when compared with C rats. In contrast, PP of GF rats had greatly reduced numbers of IgM-bearing cells (4%) when compared with C rats (23%); in some experiments virtually no IgM-bearing cells were detected. The levels of IgA- and IgE-bearing cells in spleen of GF rats were increased (to 11% and 7%, respectively). Of the IgE-bearing cells in PP and spleen of GF rats, approximately one-half were simultaneously positive for IgA. When these PP cells were treated with pronase to remove membrane bound immunoglobulins and maintained in culture, both IgE and IgA reappeared within 12 h. The proportion of doubly labeled cells was similar to that of the untreated population. No IgE+ cells were detected in bone marrow of C of GF rats at any time, in agreement with the findings of Ishizaka et al., although up to 20% of bone marrow cells bore other immunoglobulin isotypes, suggesting that IgE-bearing cells arise in the PP either de novo or by switching from precursors carrying IgM or IgA.

摘要

来自同龄成年常规饲养(C)大鼠和无菌(GF)大鼠的派尔集合淋巴结(PP)在携带不同同种型膜结合免疫球蛋白的细胞分布上存在显著差异。在大鼠的PP中发现了高浓度的膜结合IgE细胞(通过间接免疫荧光测定约占总细胞的20%),而C大鼠的PP中不存在IgE+细胞。与C大鼠相比,GF大鼠PP中的IgA+细胞数量几乎高出三倍。相比之下,与C大鼠(23%)相比,GF大鼠PP中携带IgM的细胞数量大幅减少(4%);在一些实验中几乎未检测到携带IgM的细胞。GF大鼠脾脏中携带IgA和IgE的细胞水平有所增加(分别增至11%和7%)。在GF大鼠的PP和脾脏中,约一半的携带IgE的细胞同时对IgA呈阳性。当用链霉蛋白酶处理这些PP细胞以去除膜结合免疫球蛋白并在培养中维持时,IgE和IgA在12小时内重新出现。双标记细胞的比例与未处理群体相似。在任何时候,在C或GF大鼠的骨髓中均未检测到IgE+细胞,这与石坂等人的研究结果一致,尽管高达20%的骨髓细胞携带其他免疫球蛋白同种型,这表明携带IgE的细胞要么在PP中重新产生,要么由携带IgM或IgA的前体转换而来。

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