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小鼠派尔集合淋巴结肥大细胞的体外诱导与鉴定

In vitro induction and characterization of mast cells from murine Peyer's patches.

作者信息

Kawanishi H, Ihle J M

出版信息

Scand J Immunol. 1987 Feb;25(2):109-20. doi: 10.1111/j.1365-3083.1987.tb01053.x.

Abstract

The present study was carried out in vitro to determine whether murine Peyer's patches (PP) can be a source of mucosal mast cells, using a well-defined mast cell growth factor, interleukin 3 (IL-3). The non-T, non-B, non-adherent (null) cell population of PP contained the precursor cells for mast cells. The mast cells induced possessed toluidine blue and alcian blue (pH 3)-positive granules, which were heterogeneous and contained histamine. The IL-3-induced mast cells were IL-3-dependent, did not express Ia, T-cell, B-cell or macrophage markers, and released histamine in response to Ca ionophore, but not in response to compound 48/80. These cells bore IgE-specific surface receptors and intracellular 20 alpha hydroxysteroid dehydrogenase. The latter enzyme activity was induced by IL-3 in null cells. All these features of the mast cells support the view that these cells belong to a lineage of mucosal mast cells (MMC) and are no different from those of other lymphoid tissues, such as the bone marrow and spleen. In the analysis of MMC precursor frequency, PP had a similar frequency to that of other gut-associated lymphoid tissues (mesenteric lymph nodes and lamina propria), but was much lower when compared to those of the bone marrow and spleen. Furthermore, like IL-2, PP are capable of producing IL-3 in vitro by activating their helper marker-bearing T cells. Thus, under certain conditions, such as the initial participation by PP in MMC-associated intestinal immune responses, PP are likely to provide MMC in their microenvironment, like mucosal T and B cells.

摘要

本研究在体外进行,以确定小鼠派伊尔氏结(PP)是否可作为黏膜肥大细胞的来源,研究中使用了明确的肥大细胞生长因子白细胞介素3(IL-3)。PP的非T、非B、非黏附(null)细胞群体含有肥大细胞的前体细胞。诱导产生的肥大细胞具有甲苯胺蓝和阿尔辛蓝(pH 3)阳性颗粒,这些颗粒具有异质性且含有组胺。IL-3诱导的肥大细胞依赖IL-3,不表达Ia、T细胞、B细胞或巨噬细胞标志物,对钙离子载体有反应时释放组胺,但对化合物48/80无反应。这些细胞带有IgE特异性表面受体和细胞内20α羟类固醇脱氢酶。后者的酶活性由IL-3在null细胞中诱导产生。肥大细胞的所有这些特征支持了这些细胞属于黏膜肥大细胞(MMC)谱系且与其他淋巴组织(如骨髓和脾脏)的肥大细胞无异的观点。在MMC前体频率分析中,PP的频率与其他肠道相关淋巴组织(肠系膜淋巴结和固有层)相似,但与骨髓和脾脏相比要低得多。此外,与IL-2一样,PP能够通过激活其带有辅助标志物的T细胞在体外产生IL-3。因此,在某些条件下,如PP最初参与与MMC相关的肠道免疫反应时,PP可能像黏膜T细胞和B细胞一样在其微环境中提供MMC。

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