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主要组织相容性复合体I类分子对转基因Ly49A受体的定位特异性调控

Location-specific regulation of transgenic Ly49A receptors by major histocompatibility complex class I molecules.

作者信息

Fahlén L, Khoo N K, Daws M R, Sentman C L

机构信息

Umeå Center for Molecular Pathogenesis, Umeå University, Sweden.

出版信息

Eur J Immunol. 1997 Aug;27(8):2057-65. doi: 10.1002/eji.1830270833.

Abstract

Inhibitory receptors expressed on natural killer (NK) cells and T cells specific for major histocompatibility complex (MHC) class I are believed to prevent these cells from responding to normal self tissues. To understand the regulation and function of Ly49 receptor molecules in vivo, we used the CD2 promoter to target Ly49A expression to all thymocytes, T cells, and NK cells. In animals expressing its MHC class I ligand, H-2Dd or H-2Dk, there was a large decrease in the expression of Ly49A on thymocytes, peripheral T cells, and NK1.1+ cells. The extent of the down-regulation of Ly49A was dependent on the expression of the MHC ligand for Ly49A and on the site where the cells were located. The level of expression of endogenous Ly49A was similarly found to be dependent upon the organ where the cells resided. Data from bone marrow chimeras indicated that most cell types may regulate Ly49A expression, but the efficacy to regulate receptor expression may vary depending on the cell type.

摘要

自然杀伤(NK)细胞和主要组织相容性复合体(MHC)I类特异性T细胞上表达的抑制性受体被认为可防止这些细胞对正常自身组织产生反应。为了了解Ly49受体分子在体内的调控和功能,我们使用CD2启动子将Ly49A的表达靶向所有胸腺细胞、T细胞和NK细胞。在表达其MHC I类配体H-2Dd或H-2Dk的动物中,胸腺细胞、外周T细胞和NK1.1 +细胞上Ly49A的表达大幅下降。Ly49A下调的程度取决于Ly49A的MHC配体的表达以及细胞所在的部位。同样发现内源性Ly49A的表达水平取决于细胞所在的器官。骨髓嵌合体的数据表明,大多数细胞类型可能调节Ly49A的表达,但调节受体表达的效力可能因细胞类型而异。

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