机构地区:[1]华中科技大学基础医学院生理学系,武汉430030 [2]华中科技大学基础医学国家级实验教学示范中心,武汉430030 [3]华中科技大学湖北省药物靶点和药效学评价重点实验室,武汉430030 [4]湖北民族学院病理生理学系,恩施445000 [5]黄陂区人民医院普外科,武汉430300
出 处:《生理学报》2020年第5期651-659,共9页Acta Physiologica Sinica
基 金:This work was supported by the Undergraduate Training Programs for Innovation and Entrepreneurship,China(No.HUST 16A177,201810478096)。
摘 要:本研究旨在探讨心脏成纤维细胞旁分泌能力对小鼠胚胎干细胞的影响。新生小鼠和成年小鼠成纤维细胞的条件培养基(ConM-NCF、ConM-ACF)分别稀释50倍(1:50)或5倍(1:5),通过RT-real time PCR技术、ELISA、细胞增殖检测以及计数心肌分化过程中跳动拟胚体(embryoid body, EB)的比例,观察这些条件培养基对小鼠胚胎干细胞的影响。结果显示,成纤维细胞细胞因子的分泌能力在发育过程中发生显著变化,其中白细胞介素6 (interleukin 6, IL6)随发育成熟显著增加。ConM-NCF抑制干细胞的增殖,但高、低浓度对干性基因表达的作用不同。Con M-ACF 1:50促进干细胞增殖并上调干性基因,但Con M-ACF1:5作用相反。ConM-NCF和ConM-ACF都能抑制干细胞的心肌细胞分化能力,但又各有特点:ConM-NCF 1:50抑制早期心肌分化但不影响晚期心肌细胞标记物的表达;ConM-ACF 1:50抑制早期心肌分化比ConM-NCF 1:50更显著,阻碍心肌成熟并上调分化晚期的心肌细胞标记物表达水平。此外,IL6中和抗体抑制ConM-ACF 1:50对干细胞的促增殖作用,但不影响ConMNCF 1:50的作用。干细胞分化过程中长期应用IL6中和抗体,抑制早期心肌细胞分化,但对晚期分化不产生影响。以上结果提示,心脏成纤维细胞分泌的细胞因子种类和浓度都对小鼠胚胎干细胞的增殖、干性基因表达和心肌分化有重要意义,其中ConM-ACF分泌的IL6是干细胞干性维持和心肌细胞分化的有利因素。The study aims to investigate the effects of cardiac fibroblast(CF) paracrine factors on murine embryonic stem cells(ESCs). Conditioned mediums from either neonatal cardiac fibroblasts(ConM-NCF) or adult cardiac fibroblasts(ConM-ACF) were diluted by 1:50 and 1:5, respectively, to investigate whether these conditioned mediums impact murine ESCs distinctly with RT-real time PCR techniques, cell proliferation essay, ELISA and by counting percentage of beating embryoid bodies(EBs) during ESCs differentiation. The data showed that the paracrine ability of CFs changed dramatically during development, in which interleukin 6(IL6) increased with maturation. ConM-NCF 1:50 and ConM-NCF 1:5 had opposite effects on the pluripotent markers, although they both reduced mouse ESC proliferation. ConM-ACF 1:50 promoted ESCs pluripotent markers and proliferation, while ConM-ACF 1:5 exerted negative effects. All CF-derived conditioned mediums inhibited cardiac differentiation, but with distinguishable features: Con M-NCF 1:50 slightly decreased the early cardiac differentiation without altering the maturation tendency or cardiac specific markers in EBs at differentiation of day 17;ConM-ACF 1:50 had more significant inhibitory effects on early cardiac differentiation than ConM-NCF 1:50 and impeded cardiac maturation with upregulation of cardiac specific markers. In addition, IL6 neutralization antibody attenuated positive effect of ConM-ACF 1:50 on ESCs proliferation, but had no effects on ConM-NCF 1:50. Long-term IL6 neutralization reduced the percentage of beating EBs at early developmental stage, but did not alter the late cardiac differentiation. Taken together, both the quality and quantity of factors and cytokines secreted by CFs are critical for the ESC fate. IL6 could be a favorable cytokine for ESC pluripotency and the early cardiac differentiation.
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