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CD90 serves as differential modulator of subcutaneous and visceral adipose-derived stem cells by regulating AKT activation that influences adipose tissue and metabolic homeostasis

机译:CD90通过调节影响脂肪组织和代谢稳态的AKT激活充当皮下和内脏脂肪干细胞的差异调节剂。

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摘要

S-ADSCs show higher potential in proliferation than V-ADSCs through promoting AKT activation. S-ADSCs and V-ADSCs from inguinal and epididymal adipose tissue of the mice (  = 10) were used in the following experiments. , Cell proliferation was determined by EdU incorporation assay. Fluorescence signals were examined by fluorescence microscope, and growth index (number of EdU-positive nucleiumber of all nuclei) was calculated. Representative ( ) and statistic ( ) data are shown. Scale bar 100 μm. , Colony formation was measured by crystal violet staining. Representative ( ) and statistic ( ) data are shown. Scale bar 8.5 mm. , Cell cycle profiles were analyzed by flow cytometry after PI staining. Representative ( ) and statistic ( ) data are shown. The expression of stemness genes was measured by qPCR. , Protein levels of p-AKT, AKT, and CyclinD1 were detected on S-ADSCs and V-ADSCs in the absence ( ) or presence ( ) of MK2206 (2 μM) for 20 h by western blot. Data are presented as mean ± SEM.  = 3–5 per group. *  P P
机译:通过促进AKT激活,S-ADSC比V-ADSC具有更高的增殖潜力。在以下实验中使用小鼠腹股沟和附睾脂肪组织中的S-ADSCs和V-ADSCs(= 10)。通过EdU掺入法测定细胞增殖。通过荧光显微镜检查荧光信号,并计算生长指数(EdU阳性核数/所有核数)。显示了代表性()和统计()数据。比例尺100μm。 ,通过结晶紫染色测量菌落形成。显示了代表性()和统计()数据。比例尺8.5 mm。 PI染色后,通过流式细胞仪分析细胞周期概况。显示了代表性()和统计()数据。通过qPCR测量干基因的表达。 ,通过Western blot在MK2206(2?μM)不存在(?)或存在(?)20?h的情况下,在S-ADSCs和V-ADSCs上检测到p-AKT,AKT和CyclinD1的蛋白水平。数据表示为平均值±SEM。 =每组3-5英镑。 * P P

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