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溶血磷脂酸在肠道上皮细胞增殖和分化中的作用。

Role of lysophosphatidic acid in proliferation and differentiation of intestinal epithelial cells.

机构信息

Division of Molecular and Cellular Signaling, Department of Biochemistry and Molecular Biology, Kobe University Graduate School of Medicine, Kobe, Japan.

出版信息

PLoS One. 2019 Apr 24;14(4):e0215255. doi: 10.1371/journal.pone.0215255. eCollection 2019.

Abstract

Intestinal epithelial cells (IECs) are regenerated continuously from intestinal stem cells (ISCs) near the base of intestinal crypts in order to maintain homeostasis and structural integrity of intestinal epithelium. Epidermal growth factor (EGF) is thought to be important to drive the proliferation and differentiation of IECs from ISCs, it remains unknown whether other growth factors or lipid mediators are also important for such regulation, however. Here we show that lysophosphatidic acid (LPA), instead of EGF, robustly promoted the development of intestinal organoids prepared from the mouse small intestine. Indeed, LPA exhibited the proliferative activity of IECs as well as induction of differentiation of IECs into goblet cells, Paneth cells, and enteroendocrine cells in intestinal organoids. Inhibitors for LPA receptor 1 markedly suppressed the LPA-promoted development of intestinal organoids. LPA also promoted the phosphorylation of extracellular signal-regulated kinase (ERK) 1/2 in intestinal organoids, whereas inhibition of mitogen-activated protein kinase/ERK kinase (MEK) 1/2 significantly suppressed the development of, as well as the proliferative activity and differentiation of, intestinal organoids in response to LPA. Our results thus suggest that LPA is a key factor that drives the proliferation and differentiation of IECs.

摘要

肠上皮细胞 (IECs) 从肠隐窝底部的肠干细胞 (ISCs) 中不断再生,以维持肠上皮的稳态和结构完整性。表皮生长因子 (EGF) 被认为对 ISCs 中 IECs 的增殖和分化很重要,但目前尚不清楚其他生长因子或脂质介质是否对这种调节也很重要。在这里,我们发现溶血磷脂酸 (LPA) 而不是 EGF,能强有力地促进从小鼠小肠制备的肠类器官的发育。事实上,LPA 表现出 IECs 的增殖活性,以及诱导 IECs 分化为杯状细胞、潘氏细胞和肠内分泌细胞。LPA 受体 1 的抑制剂显著抑制了 LPA 促进的肠类器官发育。LPA 还促进肠类器官中细胞外信号调节激酶 (ERK) 1/2 的磷酸化,而丝裂原活化蛋白激酶/ERK 激酶 (MEK) 1/2 的抑制则显著抑制了 LPA 诱导的肠类器官的发育,以及对 LPA 的增殖活性和分化反应。因此,我们的结果表明 LPA 是驱动 IECs 增殖和分化的关键因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a627/6481811/4acfa06f5f81/pone.0215255.g001.jpg

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