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包含外显子V6和V7的CD44亚型在有丝分裂原刺激的正常和爱泼斯坦-巴尔病毒转化的人B细胞上差异表达。

CD44 isoforms containing exons V6 and V7 are differentially expressed on mitogenically stimulated normal and Epstein-Barr virus-transformed human B cells.

作者信息

Kryworuckho M, Diaz-Mitoma F, Kumar A

机构信息

Department of Pediatrics, University of Ottawa, Ontario, Canada.

出版信息

Immunology. 1995 Sep;86(1):41-8.

Abstract

CD44, a cell adhesion molecule, exists in multiple isoforms that are generated by RNA alternative splicing. CD44 isoforms containing exon V6 (CD44 V6) have been associated with tumorigenesis and metastasis. We investigated the association between human B-cell activation and CD44 V6 isoform expression by analysing its expression in resting and mitogenically stimulated B cells. Results showed that resting B cells expressed the CD44 H (no variable exon) isoform alone. Activation of B cells [phorbol myristate acetate (PMA), surface immunoglobulin cross-linking alone or in the presence of interleukin-2 (IL-2)] induced CD44E (variable exon V8-10), R2 (VIO) and CD44 isoforms containing exons V6 and/or V7 (CD44 V6/V7). Epstein-Barr virus (EBV) infection of B cells, an alternative method of B-cell activation, induced the expression of CD44 E and R2 but not CD44 V6/V7. These results indicate that CD44 V6/V7 expression depends on the mode of activation. CD44 isoform expression was also investigated in a panel of EBV-negative and EBV-positive Burkitt's lymphoma (BL) B-cell lines. EBV-negative BL cells did not express CD44. In contrast, EBV-positive BL cells expressed CD44 H, R2 and E but not CD44 V6/V7 isoforms, suggesting an association between EBV infection and CD44 isoform induction. To determine directly the role of EBV in CD44 isoform induction, an EBV-negative BL cell line, BL30 (negative for all isoforms of CD44), BL30 infected in vitro with the EBNA-2-defective P3HR1 (BL30/P3HR1), and the wild-type B95-8 strain of EBV (BL30/B95-8) were examined. The parental BL30 cells infected with the wild-type EBV strain, but not with the P3HR-1 strain, expressed CD44 H, R2 and E isoforms, as seen in EBV-immortalized B cells. These studies suggest that (1) alternative splicing of CD44 isoforms is differentially regulated depending on the mode and state of cell activation, and that (2) the CD44 V6/V7 isoforms may represent B-cell activation antigens that are induced by mitogenic stimulation but not following EBV infection.

摘要

CD44是一种细胞黏附分子,以多种异构体形式存在,这些异构体由RNA可变剪接产生。含有外显子V6的CD44异构体(CD44 V6)与肿瘤发生和转移相关。我们通过分析其在静息和有丝分裂原刺激的B细胞中的表达,研究了人B细胞活化与CD44 V6异构体表达之间的关联。结果显示,静息B细胞仅表达CD44 H(无可变外显子)异构体。B细胞活化[佛波酯肉豆蔻酸酯乙酸酯(PMA)、单独的表面免疫球蛋白交联或在白细胞介素-2(IL-2)存在的情况下]诱导CD44E(可变外显子V8-10)、R2(VIO)以及含有外显子V6和/或V7的CD44异构体(CD44 V6/V7)。B细胞的爱泼斯坦-巴尔病毒(EBV)感染是B细胞活化的另一种方法,可诱导CD44 E和R2的表达,但不诱导CD44 V6/V7的表达。这些结果表明,CD44 V6/V7的表达取决于活化模式。我们还在一组EBV阴性和EBV阳性的伯基特淋巴瘤(BL)B细胞系中研究了CD44异构体的表达。EBV阴性的BL细胞不表达CD44。相反,EBV阳性的BL细胞表达CD44 H、R2和E,但不表达CD44 V6/V7异构体,这表明EBV感染与CD44异构体诱导之间存在关联。为了直接确定EBV在CD44异构体诱导中的作用,我们检测了一种EBV阴性的BL细胞系BL30(所有CD44异构体均为阴性)、体外感染EBNA-2缺陷型P3HR1的BL30(BL30/P3HR1)以及野生型EBV B95-8株(BL30/B95-8)。如在EBV永生化的B细胞中所见,感染野生型EBV株而非P3HR-1株的亲代BL30细胞表达CD44 H、R2和E异构体。这些研究表明:(1)CD44异构体的可变剪接受细胞活化模式和状态的差异调节;(2)CD44 V6/V7异构体可能代表由有丝分裂原刺激诱导而非EBV感染后诱导的B细胞活化抗原。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/434d/1383808/38dca941a103/immunology00062-0051-a.jpg

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