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人破骨细胞中活化T细胞核因子的表达

NFAT expression in human osteoclasts.

作者信息

Day Christopher J, Kim Michael S, Lopez Carolina M, Nicholson Geoff C, Morrison Nigel A

机构信息

School of Health Sciences, Griffith University, Gold Coast campus, Parklands Drive, Southport, Queensland 4215, Australia.

出版信息

J Cell Biochem. 2005 May 1;95(1):17-23. doi: 10.1002/jcb.20410.

Abstract

Nuclear factor of activated T-cells cytoplasmic (NFATc) is a family of transcription factors originally identified in T-cells. The gene family is currently known to have four members (NFATc1 through NFATc4) which have roles both within and outside the immune system. We show that NFATc1 is the major induced NFAT in human osteoclasts, with expression greatly exceeding that of NFATc2 through NFATc4. In macrophage-like cells in culture, NFATc1 through NFATc4 are expressed at similar low levels. NFATc1 is comprised of five mRNA transcript variants known to encode three different protein isoforms. The mRNA encoding isoform C (mRNA variant 3) was the most expressed with 38 copies per nanogram followed by isoform B (mRNA variant 5) with 17 copies per nanogram of total RNA. Isoform A (mRNA variant 1) and mRNA variants 2 and 4 made up less than 1% of the total NFATc1 expressed. NFATc1 is activated by calcineurin after calcium-calmodulin signalling. The induction of NFATc1 in osteoclasts was not altered in the presence of cyclosporin A, an inhibitor of calcineurin, suggesting that NFATc1 does not participate in autoregulatory activation of its own promoter. The NFATc1 variants expressed by human osteoclasts are not those normally expressed by effector T-cells but are similar to those seen in naïve T-cells.

摘要

活化T细胞核因子细胞质型(NFATc)是最初在T细胞中发现的一类转录因子。目前已知该基因家族有四个成员(NFATc1至NFATc4),它们在免疫系统内外均发挥作用。我们发现,NFATc1是人类破骨细胞中主要被诱导的NFAT,其表达量大大超过NFATc2至NFATc4。在培养的巨噬细胞样细胞中,NFATc1至NFATc4以相似的低水平表达。NFATc1由五个已知可编码三种不同蛋白质异构体的mRNA转录变体组成。编码异构体C(mRNA变体3)的mRNA表达量最高,每纳克有38个拷贝,其次是异构体B(mRNA变体5),每纳克总RNA有17个拷贝。异构体A(mRNA变体1)以及mRNA变体2和4占所表达的总NFATc1的比例不到1%。钙调神经磷酸酶在钙-钙调蛋白信号传导后激活NFATc1。在存在钙调神经磷酸酶抑制剂环孢素A的情况下,破骨细胞中NFATc1的诱导没有改变,这表明NFATc1不参与其自身启动子的自调节激活。人类破骨细胞表达的NFATc1变体并非效应T细胞通常表达的变体,而是与幼稚T细胞中所见的变体相似。

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