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Toll-like receptors (TLRs) have been found to contribute to the pathogenesis of rheumatoid arthritis (RA). The aim of this
study is to investigate the regulation and potential role of TLR2 in spleen of pristane-induced arthritis (PIA) rat, which
can be used to further understand the mechanisms of RA. Arthritis in DA rats was induced by pristane. TLR2 expression in spleen
was detected by real-time quantitative PCR and western blotting, and TLR2 expression at both mRNA and protein levels was upregulated
in PIA rats. Peptidoglycan (PGN) was systemically administrated to PIA rats, and arthritis severity was evaluated macroscopically
and microscopically. Results showed that systemic administration of PGN to PIA rats obviously deteriorated arthritis severity.
TLR2 expression on splenocytes and different types of immune cells was measured by flow cytometry. And it was found that TLR2
was mainly expressed on antigen-presenting cells (APCs) of spleen, and the proportion of TLR2+ dendritic cells and macrophages in spleen of PIA rats was increased remarkably. Thus, we conclude that the induction of TLR2+ APCs in spleen may participate in the maintenance of PIA. 相似文献
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净初级生产力(NPP)和净生态系统生产力(NEP)是估算陆地生态系统碳源/汇的重要指标,云南为我国碳汇的主要区域之一,开展云南NPP和NEP时空变化特征分析对科学评估陆地生态系统碳源/汇功能,以及开展碳排放交易具有重要意义。基于BEPS模型1981—2019年NPP和NEP产品,采用线性趋势分析、文献对比等方法,研究云南NPP和NEP时空变化特征及其在云南的适用性。结果表明:(1)1981—1999年云南NPP和NEP呈水平波动,2000年后云南NPP和NEP呈明显波动上升趋势,2000—2019年云南NPP高值区域主要分布在西部和南部,而NEP高值区则主要分布在东部和西部局部地区;(2)2000—2019年云南NPP和NEP除西北部部分地区为下降趋势外,其余大部地区为上升趋势;(3)云南NPP峰值出现在7、8月,谷值出现在2月,NEP峰值出现月份与NPP基本相同,但谷值出现月份较NPP滞后1—3个月,6—10月是云南碳汇的主要月份;(4)BEPS模型估算的NPP与目前广泛应用的CASA和遥感模型结果较为一致,时空变化特征与云南生态恢复措施和气候特征吻合,其估算的NEP与陆地生物圈模型... 相似文献
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The Nogo‐B receptor promotes human hepatocellular carcinoma cell growth via the Akt signal pathway
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Chengyong Dong Ying Liu Keqiu Jiang Haibo Wang Weikun Qu Chi Zhang Rui Liang Zhenming Gao Baofeng Zhao Qing Miao Shujuan Shao Liming Wang 《Journal of cellular biochemistry》2018,119(9):7738-7746
Nogo‐B receptor (NgBR) is a type I receptor with a single transmembrane domain and specifically binds to ligand Nogo‐B. A previous study demonstrated that NgBR was highly expressed in human breast invasive ductal carcinoma and promoted epithelial‐mesenchymal transition in breast tumor cells. Our recent work found that NgBR expression was associated with a poor prognosis in human patients with hepatocellular carcinoma (HCC). Here, we elucidate that the increased expression of NgBR contributes toward the increased cell growth of human HCC cells both in vitro and in vivo. Cell viability and clonogenic survival analysis results demonstrated that knockdown of NgBR inhibits the cell growth in human HCC cells, which correlates with a reduction in the phosphorylation of Akt levels. Furthermore, overexpression of NgBR by the cotransfected pIRES‐NgBR plasmid together with NgBR siRNA in human HCC cells can rescue impaired phosphorylation of Akt levels in NgBR knockdown human HCC cells. In addition, cell viability analyses showed that NgBR overexpression can rescue the cell growth inhibition presented in human HCC NgBR knockdown cells. Taken together, our results suggest that NgBR potentially acts as an oncogene in HCC by increasing Akt activity. Thus, NgBR may represent a new potential diagnostic and therapeutic target for the treatment of HCC. 相似文献
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Wenju Wang Weikun Tang Min Yan Kunyun He Lei Yang Lin Jiang Xiang Hua Li Yin Maosheng Sun Hongjun Li 《Protein expression and purification》2010,69(2):178-185
Parathyroid hormone (PTH) contributes to the increase of trabecular connectivity and is a candidate medication for effective treating osteoporosis. PTH is a protein of 84 amino acids and some studies have suggested that the active site lies within the range from amino acid (aa) 1 to 34. However, a few reports have indicated a causal relationship between PTH (aa 1–34) and osteogenic sarcoma in rats, while some less obvious but important roles of the carboxyl-terminus of PTH were also found. Unfortunately, it is difficult to obtain the active integrated PTH (1–84) in vitro, due to the instability of both the protein and its mRNA. Because an alternative translation start site is located at +25 nucleotides downstream of the true start site, a truncated PTH can be translated. We constructed a rhPTH bicistronic expression plasmid (pTrepth) that could highly express non-fusion soluble rhPTH proteins in Escherichia coli. The BL-21(DE3) containing pTrepth was cultured on a small scale until satisfactory expression and purification results were obtained. We then amplified the transformed cells in a 15-L fermentor and harvested 27 g/L cells (wet weight). Extensive rhPTH purification was achieved by a three step chromatography process. Activity tests demonstrated that our purified protein could dramatically increase cAMP in osteosarcoma cells in vitro. 相似文献
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Liesu Meng Wenhua Zhu Congshan Jiang Xiaojing He Weikun Hou Fang Zheng Rikard Holmdahl Shemin Lu 《Arthritis research & therapy》2010,12(3):R103