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生长激素给药对体内线粒体凋亡调节的影响。

The Effect of Growth Hormone Administration on the Regulation of Mitochondrial Apoptosis in-Vivo.

作者信息

Keane James, Tajouri Lotti, Gray Bon

机构信息

Faculty of Health Science and Medicine, Bond University, Gold Coast, Queensland 4227, Australia.

出版信息

Int J Mol Sci. 2015 Jun 5;16(6):12753-72. doi: 10.3390/ijms160612753.

DOI:10.3390/ijms160612753
PMID:26057745
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4490471/
Abstract

The purpose of this study was to determine whether recombinant human growth hormone (rhGH) would show any significant effects on the expression of apoptosis regulating proteins in peripheral blood mononuclear cells (PBMCs). Additionally, the potential for post-transcriptional regulation of gene expression by miRNA was assessed in two cellular compartments, the cytosol and the mitochondria. Ten male subjects were subcutaneously injected with either rhGH (1 mg) or saline (0.9%) for seven consecutive days in a double-blinded fashion. Blood sampling was undertaken prior to treatment administration and over a period of three weeks following treatment cessation. Bcl-2 and Bak gene and protein expression levels were measured in PBMCs, while attention was also directed to the expression of miR-181a and miR-125b, known translational inhibitors of Bcl-2 and Bak respectively. Results showed that rhGH significantly decreased Bak protein concentrations compared to placebo samples for up to 8 days post treatment. While cytosolic miRNA expression was not found to be significantly affected by rhGH, measurement of the expression of miR-125b in mitochondrial fractions showed a significant down-regulation eight days post-rhGH administration. These findings suggest that rhGH induces short-term anti-apoptotic effects which may be partially mediated through a novel pathway that alters the concentration of mitochondrially-associated miRNAs.

摘要

本研究的目的是确定重组人生长激素(rhGH)是否会对外周血单个核细胞(PBMCs)中凋亡调节蛋白的表达产生任何显著影响。此外,还在细胞溶质和线粒体这两个细胞区室中评估了miRNA对基因表达的转录后调控潜力。十名男性受试者以双盲方式连续七天皮下注射rhGH(1毫克)或生理盐水(0.9%)。在给药前以及停药后的三周内进行血液采样。检测PBMCs中Bcl-2和Bak基因及蛋白表达水平,同时也关注分别作为Bcl-2和Bak已知翻译抑制剂的miR-181a和miR-125b的表达。结果显示,与安慰剂样本相比,rhGH在治疗后长达8天的时间里显著降低了Bak蛋白浓度。虽然未发现rhGH对细胞溶质miRNA表达有显著影响,但rhGH给药8天后线粒体组分中miR-125b的表达量显著下调。这些发现表明,rhGH诱导短期抗凋亡效应,这可能部分通过一条改变线粒体相关miRNA浓度的新途径介导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1c/4490471/0c397d8562de/ijms-16-12753-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1c/4490471/76fde04d3bba/ijms-16-12753-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1c/4490471/d6c97570f14e/ijms-16-12753-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1c/4490471/0c397d8562de/ijms-16-12753-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1c/4490471/76fde04d3bba/ijms-16-12753-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1c/4490471/d6c97570f14e/ijms-16-12753-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1c/4490471/0c397d8562de/ijms-16-12753-g003a.jpg

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