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感染巴西日圆线虫的大鼠肥大细胞的免疫学特性

Immunologic properties of mast cells from rats infected with Nippostrongylus brasiliensis.

作者信息

Ishizaka T, König W, Kurata M, Mauser L, Ishizaka K

出版信息

J Immunol. 1975 Oct;115(4):1078-83.

PMID:51873
Abstract

The concentration of IgE in the serum of Sprague-Dawley rats increased after infection with Nippostrongylus brasiliensis (NB). The IgE concentration in normal rats was less than 1 mug/ml. After re-infection with NB, the concentration increased in 100 to 300 mug/ml. Mast cells were purified from peritoneal cells of both normal and NB-infected animals. Purified mast cells from the infected animals released histamine upon exposure to NB antigen. The antibody specific for IgE released histamine from purified mast cells of both normal and infected animals. Dose-reponse curves of histamine release suggested that mast cells from NB-infected animals bear more IgE molecules than normal mast cells. Binding of 125I-labeled rat E myeloma protein with normal mast cells was demonstrated by autoradiography. Under the same experimental conditions, mast cells of infected animals were not labeled with 125I-IgE. Mast cells from both normal and infected animals failed to combine 125I-labeled IgG. The number of IgE molecules bound per mast cell was determined by incubating 125I-labeled IgE with purified mast cells. When mast cells were incubated incubated in 0.6 to 2 mug/ml of IgE, the number of IgE molecules combined with the mast cells from infected animals was about 10% of that bound with normal mast cells. The results indicated that a large proportion of IgE receptors on mast cells of infected animals was occupied by their own IgE. No significant difference was observed between normal mast cells and those of infected animals with respect to histamine content and intracellular levels of cyclic nucleotides.

摘要

感染巴西日圆线虫(NB)后,斯普拉格 - 道利大鼠血清中的IgE浓度升高。正常大鼠的IgE浓度低于1微克/毫升。再次感染NB后,浓度升至100至300微克/毫升。从正常和感染NB的动物的腹腔细胞中纯化肥大细胞。感染动物的纯化肥大细胞在接触NB抗原后释放组胺。针对IgE的抗体从正常和感染动物的纯化肥大细胞中释放组胺。组胺释放的剂量反应曲线表明,感染NB动物的肥大细胞比正常肥大细胞携带更多的IgE分子。通过放射自显影证明了125I标记的大鼠E骨髓瘤蛋白与正常肥大细胞的结合。在相同实验条件下,感染动物的肥大细胞未被125I-IgE标记。正常和感染动物的肥大细胞均未结合125I标记的IgG。通过将125I标记的IgE与纯化的肥大细胞孵育来确定每个肥大细胞结合的IgE分子数量。当肥大细胞在0.6至2微克/毫升的IgE中孵育时,与感染动物的肥大细胞结合的IgE分子数量约为与正常肥大细胞结合数量的10%。结果表明,感染动物肥大细胞上很大一部分IgE受体被其自身的IgE占据。正常肥大细胞与感染动物的肥大细胞在组胺含量和细胞内环核苷酸水平方面未观察到显著差异。

相似文献

1
Immunologic properties of mast cells from rats infected with Nippostrongylus brasiliensis.感染巴西日圆线虫的大鼠肥大细胞的免疫学特性
J Immunol. 1975 Oct;115(4):1078-83.
2
Development of mast cells in vitro. II. Biologic function of cultured mast cells.肥大细胞的体外发育。II. 培养肥大细胞的生物学功能。
J Immunol. 1977 Jan;118(1):211-7.
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T-cell-independent and T-cell-dependent IgE responses to the nematode Nippostrongylus brasiliensis: comparison of serum IgE and mast-cell-bound IgE.针对巴西日圆线虫的非T细胞依赖性和T细胞依赖性IgE反应:血清IgE与肥大细胞结合IgE的比较
Immunology. 1995 Nov;86(3):351-5.
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IgE antibody responses in bronchoalveolar spaces of rats infected with Nippostrongylus brasiliensis.感染巴西日圆线虫的大鼠支气管肺泡空间中的IgE抗体反应。
Exp Parasitol. 1993 Feb;76(1):23-31. doi: 10.1006/expr.1993.1003.
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The role of L3T4+ and Lyt-2+ T cells in the IgE response and immunity to Nippostrongylus brasiliensis.L3T4+和Lyt-2+ T细胞在针对巴西日圆线虫的IgE反应和免疫中的作用。
J Immunol. 1988 May 1;140(9):3206-11.
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Lymphocytes bearing Fc receptors for IgE. II. Induction of Fcepsilon-receptor bearing rat lymphocytes by IgE.带有IgE Fc受体的淋巴细胞。II. IgE对携带Fcepsilon受体的大鼠淋巴细胞的诱导作用。
J Immunol. 1979 Jul;123(1):455-62.
7
Serum IgE levels during the potentiated reagin response to egg albumin in rats infected with Nippostrongylus brasiliensis.感染巴西日圆线虫的大鼠在对卵清蛋白的强化反应素反应过程中的血清免疫球蛋白E水平。
J Immunol. 1975 Jan;114(1 Pt 2):521-3.
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Increased expression of the IgE Fc receptors on rat macrophages induced by elevated serum IgE levels.血清IgE水平升高诱导大鼠巨噬细胞上IgE Fc受体表达增加。
Immunology. 1984 Sep;53(1):9-16.
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Mast cell Fc epsilonRI expression in the rat intestinal mucosa and tongue is enhanced during Nippostrongylus brasiliensis infection and can be up-regulated by in vivo administration of IgE.在巴西日圆线虫感染期间,大鼠肠黏膜和舌中肥大细胞FcεRI的表达增强,且可通过体内给予IgE上调。
J Immunol. 1997 Apr 15;158(8):3805-12.
10
Failure to obtain histamine release from rat mast cells exposed to human allergic serum and specific antigen or IgE myeloma protein and anti-IgE.未能从暴露于人类过敏血清、特异性抗原或IgE骨髓瘤蛋白及抗IgE的大鼠肥大细胞中诱导出组胺释放。
J Immunol. 1973 Oct;111(4):1022-30.

引用本文的文献

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Phagocytic cell killing mediated by secreted cytotoxic factors of Vibrio cholerae.霍乱弧菌分泌的细胞毒性因子介导的吞噬细胞杀伤作用。
Infect Immun. 2000 Sep;68(9):4930-7. doi: 10.1128/IAI.68.9.4930-4937.2000.
2
Binding characteristics of aggregated IgGa to rat basophilic leukaemia (RBL) cells and rat mast cells.聚集的IgGa与大鼠嗜碱性白血病(RBL)细胞和大鼠肥大细胞的结合特性。
Immunology. 1980 Nov;41(3):605-15.
3
Bridging of IgE receptors activates phospholipid methylation and adenylate cyclase in mast cell plasma membranes.IgE受体的桥联作用激活肥大细胞质膜中的磷脂甲基化和腺苷酸环化酶。
Proc Natl Acad Sci U S A. 1981 Nov;78(11):6812-6. doi: 10.1073/pnas.78.11.6812.
4
Immunoglobulin E-dependent stimulation of human alveolar macrophages: significance in type 1 hypersensitivity.免疫球蛋白E依赖的人肺泡巨噬细胞刺激:在1型超敏反应中的意义。
Clin Exp Immunol. 1986 Aug;65(2):416-26.
5
Simulation of parasite-induced gut hypersensitivity: implications for vaccination.寄生虫诱导的肠道超敏反应模拟:对疫苗接种的启示
Immunology. 1989 Feb;66(2):302-7.
6
Active sensitization does not increase the responsivity of rat peritoneal mast cells to diverse chemical stimuli.主动致敏不会增加大鼠腹膜肥大细胞对多种化学刺激的反应性。
Agents Actions. 1989 Apr;27(1-2):62-4. doi: 10.1007/BF02222199.
7
Purification of rat cutaneous mast cells with Percoll density centrifugation.采用Percoll密度离心法纯化大鼠皮肤肥大细胞。
Arch Dermatol Res. 1988;280(6):358-62. doi: 10.1007/BF00426614.
8
Effect of cholera toxin on histamine release from bone marrow-derived mouse mast cells.
Proc Natl Acad Sci U S A. 1988 Apr;85(8):2504-8. doi: 10.1073/pnas.85.8.2504.
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IgE synthesis in vitro during infection of mice with the nematode Nippostrongylus brasiliensis: effects of mitogens and antigens.感染巴西日圆线虫的小鼠在体外IgE的合成:丝裂原和抗原的作用
Z Parasitenkd. 1985;71(5):649-62. doi: 10.1007/BF00925598.
10
[Immune mechanism of rats on Nippostrongylus brasiliensis in vitro (author's transl)].大鼠对巴西日圆线虫体外免疫机制(作者译)
Z Parasitenkd. 1976 Jul 27;50(1):57-66. doi: 10.1007/BF00389932.