HuR mediates motility of human bone marrow-derived mesenchymal stem cells triggered by sphingosine 1-phosphate in liver fibrosis

被引：32

作者：

Chang, Na ^{[1
]}

Ge, Jingjing ^{[1
]}

Xiu, Lei ^{[1
]}

Zhao, Zhongxin ^{[1
]}

Duan, Xianghui ^{[1
]}

Tian, Lei ^{[1
]}

Xie, Jieshi ^{[1
]}

Yang, Lin ^{[1
]}

Li, Liying ^{[1
]}

机构：

[1] Capital Med Univ, Dept Cell Biol, Municipal Lab Liver Protect & Regulat Regenerat, 10 Xitoutiao, Beijing 100069, Peoples R China

来源：

JOURNAL OF MOLECULAR MEDICINE-JMM | 2017年 / 95卷 / 01期

基金：

北京市自然科学基金;

关键词：

HuR; Sphingosine; 1-phosphate; Sphingosine 1-phosphate receptor; Human mesenchymal stem cells; Liver fibrosis; BINDING PROTEIN HUR; MESSENGER-RNA-BINDING; ESSENTIAL ROLES; SPHINGOSINE-1-PHOSPHATE; EXPRESSION; CONTRIBUTES; RECEPTORS; MIGRATION; PHOSPHORYLATION; STABILIZATION;

D O I：

10.1007/s00109-016-1460-x

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Sphingosine 1-phosphate (SIP) participates in migration of bone marrow (BM)-derived mesenchymal stem cells (BMSCs) toward damaged liver via upregulation of SIP receptor 3 (S1PR3) during mouse liver fibrogenesis. But, the molecular mechanism is still unclear. HuR, as an RNA-binding protein, regulates tumor cell motility. Here, we examined the role of HuR in migration of human BMSCs (hBMSCs) in liver fibrosis. Results showed that HuR messenger RNA (mRNA) level was increased in human or mouse fibrotic livers, and correlated with S1PR3 mRNA expression. Using immunotlitorescence, we found that HuR mainly localized in the nuclei of hepatocytes and non-parenchymal cells in normal livers. However, in fibrotic livers, we detected an increased HuR cytoplasmic localization in non-parenchymal cells. In chimeric mice of BM cell-labeled by EGFP, significant numbers of EGFP-positive cells (BM origin) were positive for HuR in fibrotic areas. Meanwhile, HuR-positive cells were also positive for cx-SMA (myofibroblasts). In vitro, SIP induced hBMSCs migration via S1PR3 upregulation. HuR involved in S1P-induced hBMSCs migration and increased stabilization of S1PR3 mRNA via competing with miR-30e. RNA immunoprecipitation showed that interacted with S1PR3 mRNA 3rUTR. Moreover, SIP resulted in phosphorylation and cytoplasmic translocation of HuR via S1PR3 and p38MAPK. Furthermore, we transplanted EGFP(+) BMSCs with or without HuR small interfering RNA (siRNA) into carbon tetrachloride-treated mice and found that knockdown of HuR inhibited the migration of BMSCs toward injured livers by flow cytometric analysis in vivo. We identified a positive feedback regulation mechanism between HuR and S1PR3 in SIP induced BMSCs migration. HuR participates in upregulation of S1PR3 induced by SIP. SlP results in phosphorylation and translocation of HuR via S1PR3. Our results provide a new regulatory manner to the mechanism of liver fibrogenesis.

引用

页码：69 / 82

页数：14

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