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MS4A 和 TMEM176 基因在人 B 淋巴细胞中的表达。

Expression of MS4A and TMEM176 Genes in Human B Lymphocytes.

机构信息

Department of Biochemistry and Molecular Biology, Snyder Institute for Chronic Diseases, University of Calgary , Calgary, AB , Canada.

出版信息

Front Immunol. 2013 Jul 15;4:195. doi: 10.3389/fimmu.2013.00195. eCollection 2013.

Abstract

The MS4A gene family in humans includes CD20 and at least 15 other genes. CD20 exists as homo-oligomers in the plasma membrane, however different MS4A proteins expressed in the same cell may hetero-oligomerize. Given the importance of CD20 in B-cell function and as a therapeutic target, we sought to explore the potential for CD20 hetero-oligomerization with other MS4A proteins. We investigated expression in primary human B-cells of the four MS4A genes previously shown to be expressed in human B-cell lines (MS4A4A, MS4A6A, MS4A7, MS4A8B), as well as two genes comprising the closely related TMEM176 gene family, with a view to identifying candidates for future investigation at the protein level. TMEM176A and TMEM176B transcripts were either not detected, or were detected at relatively low levels in a minority of donor B-cell samples. MS4A4A and MS4A8B transcripts were not detected in any normal B-cell sample. MS4A6A and MS4A7 transcripts were detected at low levels in most samples, however the corresponding proteins were not at the plasma membrane when expressed as GFP conjugates in BJAB cells. We also examined expression of these genes in chronic lymphocytic leukemia (CLL), and found that it was similar to normal B-cells with two exceptions. First, whereas MS4A4A expression was undetected in normal B-cells, it was expressed in 1/14 CLL samples. Second, compared to expression levels in normal B-cells, MS4A6A transcripts were elevated in 4/14 CLL samples. In summary, none of the MS4A/TMEM176 genes tested was expressed at high levels in normal or in most CLL B-cells. MS4A6A and MS4A7 were expressed at low levels in most B-cell samples, however the corresponding proteins may not be positioned at the plasma membrane. Altogether, these data suggest that CD20 normally does not form hetero-oligomers with other MS4A proteins and that there are unlikely to be other MS4A proteins in CLL that might provide useful alternate therapeutic targets.

摘要

人类的 MS4A 基因家族包括 CD20 和至少 15 个其他基因。CD20 存在于质膜的同源寡聚体中,但在同一细胞中表达的不同 MS4A 蛋白可能异源寡聚化。鉴于 CD20 在 B 细胞功能中的重要性以及作为治疗靶点的重要性,我们试图探索 CD20 与其他 MS4A 蛋白异源寡聚化的可能性。我们研究了在原代人类 B 细胞中表达的四个 MS4A 基因(MS4A4A、MS4A6A、MS4A7、MS4A8B)的表达情况,以及两个构成密切相关 TMEM176 基因家族的基因的表达情况,以期在蛋白质水平上确定未来研究的候选基因。TMEM176A 和 TMEM176B 转录本要么未检测到,要么在少数供体 B 细胞样本中以相对较低的水平检测到。在任何正常的 B 细胞样本中均未检测到 MS4A4A 和 MS4A8B 转录本。MS4A6A 和 MS4A7 转录本在大多数样本中以低水平检测到,但当在 BJAB 细胞中表达为 GFP 缀合物时,相应的蛋白质并未位于质膜上。我们还检查了这些基因在慢性淋巴细胞白血病 (CLL) 中的表达情况,发现除了两个例外,其表达情况与正常 B 细胞相似。首先,在正常 B 细胞中未检测到 MS4A4A 的表达,但在 1/14 的 CLL 样本中表达。其次,与正常 B 细胞中的表达水平相比,MS4A6A 转录本在 14 个 CLL 样本中的 4 个样本中升高。总之,在正常或大多数 CLL B 细胞中,未测试的 MS4A/TMEM176 基因中的任何一个都没有高水平表达。MS4A6A 和 MS4A7 在大多数 B 细胞样本中以低水平表达,但相应的蛋白质可能不在质膜上。总而言之,这些数据表明 CD20 通常不会与其他 MS4A 蛋白形成异源寡聚体,并且在 CLL 中不太可能存在其他可能提供有用替代治疗靶点的 MS4A 蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c683/3711070/8324e6ba9a85/fimmu-04-00195-g001.jpg

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