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與臍帶間充質(zhì)干細胞共培養(yǎng)對乳腺上皮細胞乳脂合成及關(guān)鍵基因表達的影響

發(fā)布時間:2018-03-04 23:09

  本文選題:臍帶間充質(zhì)干細胞 切入點:乳腺上皮細胞 出處:《畜牧獸醫(yī)學(xué)報》2017年05期  論文類型:期刊論文


【摘要】:旨在探究奶牛乳腺上皮細胞(BMECs)與臍帶間充質(zhì)干細胞(UC-MSCs)共培養(yǎng)對(BMECs)乳脂合成及關(guān)鍵基因表達的影響。試驗共分為8組:共培養(yǎng)組為UC-MSCs和BMECs共培養(yǎng)條件下的不處理組、IGF-1R抑制劑AG1024處理組、Janus激酶和轉(zhuǎn)錄活化因子(JAK/STAT)信號通路信號阻斷劑AG490處理組及AG1024+AG490處理組,對照組為BMECs單培養(yǎng)條件下的不處理組、IGF-1R抑制劑AG1024組、Janus激酶和轉(zhuǎn)錄活化因子(JAK/STAT)信號通路信號阻斷劑AG490組及AG1024+AG490處理組。檢測各組上清IGF-1、甘油三酯(TG)含量變化;RT-qPCR檢測乙酰輔酶A羧化酶(ACACA),脂肪酸合成酶(FASN)和固醇調(diào)節(jié)元件結(jié)合蛋白(Sterol regulatory element binding proteins,SREBP1)基因的相對表達豐度。結(jié)果表明,共培養(yǎng)組IGF-1、TG含量均顯著高于對照組(P0.05);AG1024處理對IGF-1具有極顯著抑制效果(P0.01),顯著降低TG含量及ACACA、FASN、SREBP1mRNA相對表達豐度(P0.05);AG490處理對ACACA、FASN、SREBP1mRNA的表達無顯著影響(P0.05);AG1024和AG490共同處理較AG1024單獨處理各項指標(biāo)表現(xiàn)差異不顯著(P0.05)。綜上表明,臍帶間充質(zhì)干細胞能夠通過IGF-1促進乳腺上皮細胞乳脂合成及關(guān)鍵基因的表達,JAK2/STAT5信號通路不參與臍帶間充質(zhì)干細胞對乳腺上皮細胞乳脂調(diào)控。
[Abstract]:To investigate the effects of co-culture of bovine mammary epithelial cells (BMECs) and umbilical cord mesenchymal stem cells (UC-MSCs) on the synthesis of milk fat and expression of key genes in the milk of BMC cells. The experiment was divided into 8 groups: the co-culture group was untreated under the condition of UC-MSCs and BMECs co-culture. IGF-1R inhibitor AG1024 treatment group, AG490 treatment group and AG1024 AG490 treatment group, The control group was treated with BMECs mono-culture. The level of IGF-1R inhibitor AG1024 was detected by RT-qPCR. The signal pathway blocker AG490 and AG1024 AG490 were used to detect the IGF-1 and triglyceride TGs in the supernatant of each group. The relative expression abundance of acetyl coenzyme A carboxylase, fatty acid synthase (FASN) and sterol regulatory element binding proteins1 (SREBP1) gene was observed. The content of IGF-1G in co-cultured group was significantly higher than that in control group (P0.05AG-1024). The effect of P0.01C on IGF-1 was significantly lower than that of P0.01treatment, and the relative expression abundance of ACA FASNNU SREBP1mRNA and the relative expression of ACA FASNN SREBP1 mRNA were not affected by ACA FASNN SREBP1 mRNA expression in ACA FASNSREBP1 treated with ACA FASNN AG1024 and AG490 alone. The results showed that the expression of ACA FASNSREBP1 mRNA was not affected by ACA FASNN AG1024 and AG490 alone. There was no significant difference in the performance of various indexes between the two groups (P 0.05). Umbilical cord mesenchymal stem cells can promote breast epithelial cell milk fat synthesis and expression of key genes through IGF-1. JAK2 / STAT5 signaling pathway does not participate in the regulation of breast epithelial cell milk fat by umbilical cord mesenchymal stem cells.
【作者單位】: 新疆農(nóng)業(yè)大學(xué)動物科學(xué)學(xué)院新疆肉乳用草食動物營養(yǎng)實驗室;
【基金】:奶產(chǎn)業(yè)體系資助(CARS-37) 國家自然科學(xué)基金(31560645) 中國博士后基金 新疆維吾爾自治區(qū)高等學(xué)校科研計劃項目(XJEDU2013S17) 2013年度新疆研究生科研創(chuàng)新項目(xjau-2013-yjsky-XJGRI2013113) 新疆肉乳用草食動物營養(yǎng)實驗室開放課題
【分類號】:S823

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