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人类Thy-1基因在啮齿动物-人类体细胞杂种中的差异表达[已校正]

Differential expression of the human Thy-1 gene in rodent-human somatic cell hybrids [corrected].

作者信息

Rettig W J, Nishimura H, Yenamandra A K, Seki T, Obata F, Beresford H R, Old L J, Silver J

出版信息

J Immunol. 1987 Jun 15;138(12):4484-9.

PMID:2884261
Abstract

Thy-1 is a cell surface differentiation marker which shows distinct patterns of tissue-specific expression in different species. In man, the Thy-1 antigen is encoded by chromosome 11. We have examined the regulatory signals determining human Thy-1 expression through serologic analysis of rodent-human somatic cell hybrids retaining human chromosome 11 in which the fusion partners belong to distinct differentiation lineages. Cell surface expression of human Thy-1 was determined by mixed hemadsorption assays with two monoclonal antibodies (mAb), K117 and L127, shown to detect authentic human Thy-1 through analysis of COS-7 monkey kidney cells transfected with a cloned human Thy-1 gene. Three different patterns of human Thy-1 expression were observed when hybrid cells, constructed with different human and rodent cell types, were tested with mAb K117 and L127. Hybrids formed between Thy-1+ human neuroblastoma cells and Thy-1- mouse neuroblastoma cells, or hybrids between Thy-1+ human fibroblasts and the Thy-1- mouse kidney carcinoma, RAG, retain human Thy-1 expression. In contrast, hybrids formed between either Thy-1+ human neuroblastoma cells or Thy-1+ human fibroblasts and Thy-1- mouse L cells lose expression of human Thy-1 even though chromosome 11 is retained. Finally, hybrids formed between Thy-1- human peripheral lymphocytes or a Thy-1- lymphoblastoid B cell line and Thy-1- Chinese hamster fibroblasts begin to express human Thy-1. These studies suggest that both positive and negative trans-acting signals may play a role in the tissue-specific regulation of the human Thy-1 gene.

摘要

Thy-1是一种细胞表面分化标志物,在不同物种中呈现出不同的组织特异性表达模式。在人类中,Thy-1抗原由11号染色体编码。我们通过对保留人类11号染色体的啮齿动物-人类体细胞杂种进行血清学分析,研究了决定人类Thy-1表达的调控信号,其中融合亲本属于不同的分化谱系。通过用两种单克隆抗体(mAb)K117和L127进行混合血细胞吸附试验来确定人类Thy-1的细胞表面表达,通过对转染了克隆人类Thy-1基因的COS-7猴肾细胞进行分析,这两种抗体被证明可检测到真实的人类Thy-1。当用不同的人类和啮齿动物细胞类型构建的杂种细胞用mAb K117和L127进行检测时,观察到了三种不同的人类Thy-1表达模式。Thy-1阳性的人类神经母细胞瘤细胞与Thy-1阴性的小鼠神经母细胞瘤细胞之间形成的杂种,或Thy-1阳性的人类成纤维细胞与Thy-1阴性的小鼠肾癌RAG之间形成的杂种,保留了人类Thy-1的表达。相反,Thy-1阳性的人类神经母细胞瘤细胞或Thy-1阳性的人类成纤维细胞与Thy-1阴性的小鼠L细胞之间形成的杂种,即使保留了11号染色体,也会失去人类Thy-1的表达。最后,Thy-1阴性的人类外周淋巴细胞或Thy-1阴性的淋巴母细胞样B细胞系与Thy-1阴性的中国仓鼠成纤维细胞之间形成的杂种开始表达人类Thy-1。这些研究表明,正向和负向反式作用信号可能在人类Thy-1基因的组织特异性调控中发挥作用。

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