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白细胞介素-1β诱导的自噬相关基因 5 调节胚胎干细胞源性成牙本质细胞的增殖。

Interleukin-1β-induced autophagy-related gene 5 regulates proliferation of embryonic stem cell-derived odontoblastic cells.

机构信息

Department of Endodontics, School of Dentistry, Aichi Gakuin University, 2-11 Suemori-dori, Chikusa-ku, Nagoya, Aichi, 464-8651, Japan.

Department of Medicinal Biochemistry, School of Pharmacy, Aichi Gakuin University, 1-100 Kusumoto, Chikusa-ku, Nagoya, 464-8650, Japan.

出版信息

PLoS One. 2015 Apr 20;10(4):e0124542. doi: 10.1371/journal.pone.0124542. eCollection 2015.

Abstract

We previously established a method for the differentiation of induced pluripotent stem cells and embryonic stem cells into α2 integrin-positive odontoblast-like cells. We also reported that Wnt5 in response to interleukin (IL)-1β induces matrix metalloproteinase (MMP)-3-regulated cell proliferation in these cells. Our findings suggest that MMP-3 plays a potentially unique physiological role in the generation of odontoblast-like cells under an inflammatory state. Here, we examined whether up-regulation of autophagy-related gene (Atg) 5 by IL-1β was mediated by Wnt5 signaling, thus leading to increased proliferation of odontoblast-like cells. IL-1β increased the mRNA and protein levels of Atg5, microtubule-associated protein 1 light chain (LC3, a mammalian homolog of yeast Atg8) and Atg12. Treatment with siRNAs against Atg5, but not LC3 and Atg12, suppressed the IL-1β-induced increase in MMP-3 expression and cell proliferation. Our siRNA analyses combined with western blot analysis revealed a unique sequential cascade involving Atg5, Wnt5a and MMP-3, which resulted in the potent increase in odontoblastic cell proliferation. These results demonstrate the unique involvement of Atg5 in IL-1β-induced proliferation of embryonic stem cell-derived odontoblast-like cells.

摘要

我们之前建立了一种方法,可将诱导多能干细胞和胚胎干细胞分化为 α2 整合素阳性的成牙本质样细胞。我们还报告称,白细胞介素 (IL)-1β 作用下的 Wnt5 可诱导这些细胞中基质金属蛋白酶 (MMP)-3 调节的细胞增殖。我们的研究结果表明,MMP-3 在炎症状态下成牙本质样细胞的产生中发挥潜在独特的生理作用。在这里,我们研究了白细胞介素 (IL)-1β 是否通过 Wnt5 信号上调自噬相关基因 (Atg) 5,从而导致成牙本质样细胞增殖增加。IL-1β 增加了 Atg5、微管相关蛋白 1 轻链 (LC3,酵母 Atg8 的哺乳动物同源物) 和 Atg12 的 mRNA 和蛋白水平。用针对 Atg5 的 siRNA 处理,但不是 LC3 和 Atg12 的 siRNA,抑制了 IL-1β 诱导的 MMP-3 表达和细胞增殖增加。我们的 siRNA 分析结合 Western blot 分析揭示了一种独特的级联反应,涉及 Atg5、Wnt5a 和 MMP-3,从而导致成牙本质细胞增殖的强烈增加。这些结果表明 Atg5 独特地参与了白细胞介素 (IL)-1β 诱导的胚胎干细胞源性成牙本质样细胞增殖。

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