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首页> 外文期刊>Cell cycle >Exogenous expression of SAMHD1 inhibits proliferation and induces apoptosis in cutaneous T-cell lymphoma-derived HuT78 cells
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Exogenous expression of SAMHD1 inhibits proliferation and induces apoptosis in cutaneous T-cell lymphoma-derived HuT78 cells

机译:Samhd1的外源表达抑制了皮肤T细胞淋巴瘤衍生HUT78细胞中凋亡的增殖和诱导细胞凋亡

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摘要

Sterile a motif and HD domain-containing protein 1 (SAMHD1) is a mammalian dNTP hydrolase (dNTPase) that regulates intracellular dNTP balance. We have previously reported that SAMHD1 mRNA and protein levels are significantly downregulated in CD4(+) T-cells of patients with cutaneous T-cell lymphoma (CTCL), a disease characterized by infiltration of neoplastic CD4(+) T-lymphocytes into the skin. However, functional significance of SAMHD1 in CTCL development and progression remains unknown. Here we investigate the mechanism by which SAMHD1 induces apoptosis in CTCL-derived CD4(+) T-cells. We stably expressed exogenous SAMHD1 in the CTCL-derived HuT78 T-cell line containing a very low level of endogenous SAMHD1 protein. We found that low-level exogenous expression of SAMHD1 led to a significant reduction in HuT78 cell growth, proliferation, and colony formation. Exogenous SAMHD1 expression in HuT78 cells also resulted in increased spontaneous and Fas ligand (Fas-L)-induced apoptosis levels via activation of the extrinsic pathway, including caspase-8, -3 and -7. Additionally, increased SAMHD1 significantly reduced the protein and mRNA expression of the short isoform of cFLIP (cFLIPS), an important negative regulator of Fas-L-mediated apoptotic signaling. Our results indicate that exogenous SAMHD1 expression inhibits HuT78 cell growth and proliferation in part by increasing apoptosis. These findings implicate that SAMHD1 acts as an inhibitor in CTCL cell growth, suggesting that downregulation of SAMHD1 expression in neoplastic T-cells can facilitate uncontrolled cell proliferation.
机译:无菌MOTIF和含HD结构域的蛋白质1(SAMHD1)是调节细胞内DNTP平衡的哺乳动物DNTP水解酶(DNTP酶)。我们此前据报道,SAMHD1 mRNA和蛋白质水平在皮肤T细胞淋巴瘤(CTCL)的患者的CD4(+)T细胞中显着下调,一种疾病,其特征在于肿瘤CD4(+)T淋巴细胞进入皮肤。然而,Samhd1在CTCL开发和进展中的功能意义仍然未知。在这里,我们研究了Samhd1在CTCl衍生的CD4(+)T细胞中诱导细胞凋亡的机制。我们在CTCl衍生的Hut78 T细胞系中稳定表达外源性Samhd1,含有非常低的内源性Samhd1蛋白。我们发现Samhd1的低级外源性表达导致Hut78细胞生长,增殖和菌落形成的显着降低。 Hut78细胞中的外源性Samhd1表达也导致自发性和Fas配体(Fas-1)诱导的细胞凋亡水平,通过外本途径激活,包括Caspase-8,-3和-7。另外,增加的SamHD1显着降低了Clip(CFlips)短同种型的蛋白质和mRNA表达,是Fas-L介导的凋亡信号传导的重要负调节剂。我们的结果表明,外源性Samhd1表达通过增加凋亡抑制了Hut78细胞生长和增殖。这些发现涉及SAMHD1作为CTCL细胞生长中的抑制剂,表明在肿瘤T细胞中的SamHD1表达的下降可以促进不受控制的细胞增殖。

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  • 来源
    《Cell cycle》 |2017年第2期|共10页
  • 作者单位

    Ohio State Univ Dept Vet Biosci Ctr Retrovirus Res 1900 Coffey Rd Columbus OH 43210 USA;

    Ohio State Univ Dept Vet Biosci Ctr Retrovirus Res 1900 Coffey Rd Columbus OH 43210 USA;

    Ohio State Univ Dept Vet Biosci Ctr Retrovirus Res 1900 Coffey Rd Columbus OH 43210 USA;

    Ohio State Univ Dept Vet Biosci Ctr Retrovirus Res 1900 Coffey Rd Columbus OH 43210 USA;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 细胞生物学;
  • 关键词

    apoptosis; cell proliferation; cFLIP; Fas-L; lymphoma; SAMHD1;

    机译:细胞凋亡;细胞增殖;CFLIP;FAS-L;淋巴瘤;SAMHD1;

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