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小鼠嗜酸性粒细胞增多症的遗传控制:骨髓来源细胞中表达的基因控制高反应性。

Genetic control of eosinophilia in mice: gene(s) expressed in bone marrow-derived cells control high responsiveness.

作者信息

Vadas M A

出版信息

J Immunol. 1982 Feb;128(2):691-5.

PMID:7054293
Abstract

A heterogeneity in the capacity of strains of mice to mount eosinophilia is described. BALB/c and C3H are eosinophil high responder strains (EO-HR) and CBA and A/J are eosinophil low responder strains (EO-LR), judged by the response of blood eosinophils to Ascaris suum, and the response of blood, bone marrow, and spleen eosinophils to keyhole limpet hemocyanin given 2 days after 150 mg/kg cyclophosphamide. Some of the gene(s) for high responsiveness appear to be dominant because (EO-HR X EO-LR)F1 mice were intermediate to high responders. This gene is expressed in bone marrow-derived cells because radiation chimeras of the type EO-HR leads to F1 were high responders and EO-LR leads to F1 were low responders. This description of a genetic control of eosinophilia in mice may be useful in understanding the role of this cell in parasite immunity and allergy.

摘要

本文描述了小鼠品系引发嗜酸性粒细胞增多能力的异质性。通过血液嗜酸性粒细胞对猪蛔虫的反应,以及血液、骨髓和脾脏嗜酸性粒细胞对150mg/kg环磷酰胺注射2天后给予的匙孔血蓝蛋白的反应来判断,BALB/c和C3H是嗜酸性粒细胞高反应品系(EO-HR),而CBA和A/J是嗜酸性粒细胞低反应品系(EO-LR)。一些高反应性基因似乎是显性的,因为(EO-HR×EO-LR)F1小鼠的反应介于高反应者和中等反应者之间。该基因在骨髓来源的细胞中表达,因为EO-HR→F1类型的辐射嵌合体是高反应者,而EO-LR→F1类型的辐射嵌合体是低反应者。对小鼠嗜酸性粒细胞增多的遗传控制的这种描述可能有助于理解这种细胞在寄生虫免疫和过敏中的作用。

相似文献

1
Genetic control of eosinophilia in mice: gene(s) expressed in bone marrow-derived cells control high responsiveness.小鼠嗜酸性粒细胞增多症的遗传控制:骨髓来源细胞中表达的基因控制高反应性。
J Immunol. 1982 Feb;128(2):691-5.
2
Cyclophosphamide pretreatment induces eosinophilia to nonparasite antigens.环磷酰胺预处理可诱导对非寄生虫抗原产生嗜酸性粒细胞增多。
J Immunol. 1981 Nov;127(5):2083-6.
3
Sequential analysis of the virus-immune responder characteristics of thymocytes from F1 leads to parent radiation chimeras.对来自F1代至亲代辐射嵌合体的胸腺细胞的病毒免疫应答特征进行序列分析。
Thymus. 1982 May;4(3):119-33.
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Genetic control of eosinophilia. Mouse strain variation in response to antigens of parasite origin.嗜酸性粒细胞增多症的遗传控制。小鼠品系对寄生虫来源抗原反应的差异。
Clin Exp Immunol. 1983 Feb;51(2):239-46.
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Early dominance of irradiated host cells in the responder profiles of thymocytes from P leads to F1 radiation chimeras.在P品系胸腺细胞的应答谱中,受辐照宿主细胞的早期优势导致F1辐射嵌合体的形成。
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Genetic control of bone marrow transplantation in irradiated mice: classification of mouse strains according to their responsiveness to bone marrow allografts and xenografts.受辐照小鼠骨髓移植的遗传控制:根据小鼠品系对骨髓同种异体移植和异种移植的反应性进行分类
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Long-term survival of murine allogeneic bone marrow chimeras: effect of anti-lymphocyte serum and bone marrow dose.小鼠同种异体骨髓嵌合体的长期存活:抗淋巴细胞血清和骨髓剂量的影响。
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Bone-marrow eosinophilia in the mouse. II. Eosinophil leukocyte levels in mice injected with egg-white and Freund's adjuvant.小鼠骨髓嗜酸性粒细胞增多症。II. 注射卵清蛋白和弗氏佐剂的小鼠嗜酸性粒细胞水平
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Relationship between interleukin-5 and eotaxin in regulating blood and tissue eosinophilia in mice.白细胞介素-5与嗜酸性粒细胞趋化因子在调节小鼠血液和组织嗜酸性粒细胞增多中的关系。
J Clin Invest. 1997 Mar 1;99(5):1064-71. doi: 10.1172/JCI119234.

引用本文的文献

1
Genetic control of eosinophilia. Mouse strain variation in response to antigens of parasite origin.嗜酸性粒细胞增多症的遗传控制。小鼠品系对寄生虫来源抗原反应的差异。
Clin Exp Immunol. 1983 Feb;51(2):239-46.
2
Evidence for the control of eosinophilia by the major histocompatibility complex in mice.小鼠主要组织相容性复合体对嗜酸性粒细胞增多症控制作用的证据。
Immunogenetics. 1983;17(2):167-77. doi: 10.1007/BF00364756.
3
The effect of eosinophil chemotactic factors on in vitro eosinopoiesis in the guinea pig.嗜酸性粒细胞趋化因子对豚鼠体外嗜酸性粒细胞生成的影响。
Blut. 1983 Nov;47(5):287-96. doi: 10.1007/BF00319898.
4
New properties and roles for eosinophils in disease: discussion paper.嗜酸性粒细胞在疾病中的新特性与作用:讨论文件
J R Soc Med. 1985 Oct;78(10):844-8. doi: 10.1177/014107688507801011.
5
Genetic control of eosinophilia. Analysis of production and response to eosinophil-differentiating factor in strains of mice infected with Trichinella spiralis.嗜酸性粒细胞增多症的遗传控制。对感染旋毛虫的小鼠品系中嗜酸性粒细胞分化因子的产生及反应的分析。
Clin Exp Immunol. 1989 Jul;77(1):137-43.