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HOXB基因在活化的成人T淋巴细胞中的协同表达及增殖作用

Coordinate expression and proliferative role of HOXB genes in activated adult T lymphocytes.

作者信息

Carè A, Testa U, Bassani A, Tritarelli E, Montesoro E, Samoggia P, Cianetti L, Peschle C

机构信息

Department of Hematology and Oncology, Istituto Superiore di Sanità, Rome, Italy.

出版信息

Mol Cell Biol. 1994 Jul;14(7):4872-7. doi: 10.1128/mcb.14.7.4872-4877.1994.

Abstract

We investigated the expression of HOXB cluster genes in purified phytohemagglutinin (PHA)-activated T lymphocytes from normal adult peripheral blood by reverse transcription PCR and RNase protection. These genes are not expressed in quiescent T cells, except for barely detectable B1 RNA. After the PHA stimulus, HOXB gene activation initiates coordinately as a rapid induction wave in the 3'-->5' cluster direction (i.e., from HOXB1 through B9 genes). Thus, (i) expression of the foremost 3'-located B1 and B2 genes peaks 10 min after PHA addition and then rapidly declines, (ii) activation of B3, B4, and B5 begins 10 min after PHA addition and peaks at later times (i.e., at 120 min for B5), (iii) B6, B7, and B9 are expressed at a low level starting at later times (45 to 60 min), and (iv) B8 remains silent. Treatment of PHA-activated T lymphocytes with antisense oligonucleotides to B2 or B4 mRNA causes a drastic inhibition of T-cell proliferation and a decreased expression of T-cell activation markers (i.e., interleukin 2 and transferrin receptors). Similarly, treatment of CEM-CCRF, Peer, and SEZ627 T acute lymphocytic leukemia cell lines with anti-B4 oligomer markedly inhibits cell proliferation. Finally, T cells stimulated by a low dosage of PHA in the presence of 1 microM retinoic acid show a marked increase of both HOXB expression, particularly B2, and cell proliferation. These studies provide novel evidence on the role of HOX genes in adult cell proliferation. (i) Coordinate, early activation of HOXB genes from the 3'-->5' cluster side apparently underlies T-cell activation. (ii) The expression pattern in adult PHA-activated T cells is strikingly similar to that observed in retinoic acid-induced teratocarcinoma cells (A. Simeone, D. Acampora, L. Arcioni, P. W. Andres, E. Boncinelli, and F. Mavilio, Nature (London) 346:763-766, 1990), thus suggesting that molecular mechanisms underlying HOX gene expression in the earliest stages of development may also operate in activated adult T lymphocytes.

摘要

我们通过逆转录聚合酶链反应(RT-PCR)和核糖核酸酶保护法,研究了正常成人外周血中经植物血凝素(PHA)激活的纯化T淋巴细胞中HOXB基因簇的表达情况。除了几乎检测不到的B1 RNA外,这些基因在静止T细胞中不表达。PHA刺激后,HOXB基因的激活以快速诱导波的形式在3'→5'基因簇方向(即从HOXB1到B9基因)协同启动。因此,(i)最靠近3'端的B1和B2基因在添加PHA后10分钟表达达到峰值,然后迅速下降;(ii)B3、B4和B5的激活在添加PHA后10分钟开始,并在稍后时间达到峰值(例如,B5在120分钟达到峰值);(iii)B6、B7和B9在较晚时间(45至60分钟)开始低水平表达;(iv)B8保持沉默。用针对B2或B4 mRNA的反义寡核苷酸处理PHA激活的T淋巴细胞,会导致T细胞增殖受到严重抑制,且T细胞激活标志物(即白细胞介素2和转铁蛋白受体)的表达降低。同样,用抗B4寡聚物处理CEM-CCRF、Peer和SEZ627 T急性淋巴细胞白血病细胞系,可显著抑制细胞增殖。最后,在1 microM视黄酸存在的情况下,用低剂量PHA刺激的T细胞显示HOXB表达,特别是B2表达以及细胞增殖均显著增加。这些研究为HOX基因在成人细胞增殖中的作用提供了新的证据。(i)HOXB基因从3'→5'基因簇一侧的协同早期激活显然是T细胞激活的基础。(ii)成人PHA激活的T细胞中的表达模式与在视黄酸诱导的畸胎癌细胞中观察到的模式惊人地相似(A. Simeone、D. Acampora、L. Arcioni、P. W. Andres、E. Boncinelli和F. Mavilio,《自然》(伦敦)346:763 - 766,1990),因此表明在发育最早阶段HOX基因表达的分子机制可能也在激活的成人T淋巴细胞中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e04/358859/f22299d6f68c/molcellb00007-0550-a.jpg

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