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黄芪多糖对C3H10T1/2细胞棕色脂肪分化中长链非编码RNA表达谱的影响
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作者 张世和 曹宇鑫 +2 位作者 邓步皓 高旭阳 赵俊星 《激光生物学报》 CAS 2020年第4期333-343,351,共12页
本试验旨在探究黄芪多糖(APS)对小鼠间充质干细胞C3H10T1/2细胞棕色脂肪化过程中长链非编码RNA(lncRNA)表达谱的影响。试验以C3H10T1/2细胞为研究对象,在成脂诱导分化培养液中添加0.4 g/L的APS,以诱导分化1.5 d的细胞构建文库后测序,筛... 本试验旨在探究黄芪多糖(APS)对小鼠间充质干细胞C3H10T1/2细胞棕色脂肪化过程中长链非编码RNA(lncRNA)表达谱的影响。试验以C3H10T1/2细胞为研究对象,在成脂诱导分化培养液中添加0.4 g/L的APS,以诱导分化1.5 d的细胞构建文库后测序,筛选差异mRNAs和差异lncRNAs,并对差异mRNAs和差异lncRNAs的顺式及共表达作用预测的靶基因进行了功能分析。通过荧光定量PCR随机分析了3个lncRNAs和3个mRNAs的表达水平,验证了测序结果的准确性。研究结果表明,本次测序共得到13450个lncRNAs和57776个mRNAs。通过对其表达量、长度、外显子个数和成对重复性检验分析证明了测序数据的可靠性较好。筛选共得到153个差异表达的lncRNAs和1238个差异表达的mRNAs。结果表明,差异mRNAs主要基因本体(GO)注释富集在53个功能分类中,京都基因与基因组百科全书(KEGG)分析富集在343条通路中。差异lncRNAs顺式及共表达作用预测的靶基因GO注释分别富集在34和33个功能分类中,在分子功能中条目一致。KEGG分析显示,多个基因富集在脂肪代谢和脂肪分化的信号通路中,尤其在胰高血糖素及cAMP信号通路中富集显著。综上表明,APS导致了C3H10T1/2细胞成脂分化中lncRNA表达谱的变化。本研究结果可为进一步解析APS对干细胞的分化调节提供科学依据。 展开更多
关键词 黄芪多糖 lncRNAs C3H10T1/2 棕色脂肪分化 表达谱
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Human fetal mesenchymal stem cells differentiate into brown and white adipocytes: a role for ERRα in human UCP1 expression 被引量:5
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作者 Daniel L Morganstein Pensee Wu +3 位作者 Meritxell R Mane Nick M Fisk Roger White Malcolm G Parker 《Cell Research》 SCIE CAS CSCD 2010年第4期434-444,共11页
We investigated the ability of fetal mesenchymal stem cells (fMSCs) to differentiate into brown and white adi- pocytes and compared the expression of a number of marker genes and key regulatory factors. We showed th... We investigated the ability of fetal mesenchymal stem cells (fMSCs) to differentiate into brown and white adi- pocytes and compared the expression of a number of marker genes and key regulatory factors. We showed that the expression of key adipocyte regulators and markers during differentiation is similar to that in other human and mu- rine adipocyte models, including induction of PPARy2 and FABP4. Notably, we found that the preadipocyte marker, Pref-1, is induced early in differentiation and then declines markedly as the process continues, suggesting that fMSCs first acquire preadipocyte characteristics as they commit to the adipogenic lineage, prior to their differentiation into mature adipocytes. After adipogenic induction, some stem cell isolates differentiated into cells resembling brown adi- pocytes and others into white adipocytes. Detailed investigation of one isolate showed that the novel brown fat-deter- mining factor PRDM16 is expressed both before and after differentiation. Importantly, these cells exhibited elevated basal UCP-1 expression, which was dependent on the activity of the orphan nuclear receptor ERRa, highlighting a novel role for ERRa in human brown fat. Thus fMSCs represent a useful in vitro model for human adipogenesis, and provide opportunities to study the stages prior to commitment to the adipocyte lineage. They also offer invaluable in- sights into the characteristics of human brown fat. 展开更多
关键词 mesenchymal stem cells ADIPOGENESIS ADIPOCYTES BROWN prdm16 ucpl ERRα
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Zic1 negatively regulates brown adipogenesis in C_3H_(10)T_(1/2) cells 被引量:1
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作者 张瀚林 黄园园 +1 位作者 李赫钟 金万洙 《Science Bulletin》 SCIE EI CAS CSCD 2015年第11期1033-1035,I0008,共4页
Zinc finger in the cerebellum 1 (Zicl) is known to regulate neurogenesis and myogenesis in the develop- mental stage and widely used as one of the brown adipocyte-specific markers. In this study, we examined the eff... Zinc finger in the cerebellum 1 (Zicl) is known to regulate neurogenesis and myogenesis in the develop- mental stage and widely used as one of the brown adipocyte-specific markers. In this study, we examined the effect of Zicl on brown adipogenesis. Overexpression of Zicl attenuated the lipid accumulation and the expressions of PPAR72 and C/EBPα in C3H10T1/2 mesenchymal stem cells. The mRNA levels of BAT-specific thermogenic genes (PRDM16, PGC-1α and UCP1) and fatty acid oxidation regulatory genes (PPARα, CPT1α, CPT1β and COX7α1) were suppressed in Zicl-overexpressed cells. Moreover, overexpression of Zicl reduced the mitochondrial oxidative phosphorylation (OXPHOS) regulatory proteins including ATP5α, UQCRC2, SDHB and NDUFB5. These results indicate a potential role of Zicl in the regulation of brown adipogenesis via inhibiting adipogenesis, fatty acid oxidation and mitochondrial OXPHOS. 展开更多
关键词 Zic1 - Brown adipogenesis Fatty acid oxidation OXPHOS
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