Wisp2 disruption represses Cxcr4 expression and inhibits BMSCs homing to injured liver
Qin, Dan1; Yan, Yi1; Hu, Bian2; Zhang, Wanpo1; Li, Hanmin3; Li, Xiaodong3; Liu, Shenghui1; Dai, Depeng1; Hu, Xiongji1; Huang, Xingxu2; Zhang, Lisheng1
2017-11-17
Source PublicationONCOTARGET
ISSN1949-2553
Volume8Issue:58Pages:98823-98836
Status已发表
DOI10.18632/oncotarget.22006
AbstractLiver regeneration/repair is a compensatory regrowth following acute liver failure, and bone marrow-derived mesenchyme stem cell (BMSC) transplantation is an effective therapy that promotes liver regeneration/repair. Wnt1 inducible signaling pathway protein 2 (Wisp2) is highly expressed in BMSCs, however, its function remains unclear. In this work, we used clustered regularly interspaced short palindromic repeats (CRISPR)-associated protein -9 nuclease (CRISPR/Cas9) genome editing technology to knockdown Wisp2 in BMSCs, and these modified cells were then transplanted into rats which were induced by the 2-AAF/PH. By linking the expression of Cas9 to green fluorescent protein (GFP), we tracked BMSCs in the rats. Disruption of Wisp2 inhibited the homing of BMSCs to injured liver and aggravated liver damage as indicated by remarkably high levels of ALT and AST. Moreover, the key factor in BMSC transplantation, C-X-C chemokine receptor type 4 (Cxcr4), was down-regulated in the Wisp2 depleted BMSCs and had a lower expression in the livers of the corresponding rats. By tracing the GFP marker, more BMSCs were observed to differentiate into CD31 positive endothelial cells in the functional Wisp2 cells but less in the Wisp2 gene disrupted cells. In summary, Wisp2 promotes the homing of BMSCs through Cxcr4 related signaling during liver repair in rats.
Keywordrat Wisp2 Cxcr4 BMSCs homing
Indexed BySCI
Language英语
Funding ProjectFundamental Research Funds for the Central Universities[2662017PY106] ; Fundamental Research Funds for the Central Universities[2662016PY087]
WOS Research AreaOncology ; Cell Biology
WOS SubjectOncology ; Cell Biology
WOS IDWOS:000419392300087
PublisherIMPACT JOURNALS LLC
WOS KeywordMARROW STROMAL CELLS ; STEM-CELLS ; GROWTH-FACTOR ; MIGRATION ; CANCER ; GENE ; TRANSPLANTATION ; PATHWAY ; TISSUE
Original Document TypeArticle
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Cited Times:1[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttps://kms.shanghaitech.edu.cn/handle/2MSLDSTB/16294
Collection生命科学与技术学院_PI研究组_黄行许组
Corresponding AuthorZhang, Lisheng
Affiliation1.Univ Huazhong Agr, Coll Vet Med, Wuhan 430070, Hubei, Peoples R China
2.Shanghai Tech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
3.Hubei Prov Hosp Tradit Chinese Med, Hepat Dis Inst, Wuhan 430061, Hubei, Peoples R China
Recommended Citation
GB/T 7714
Qin, Dan,Yan, Yi,Hu, Bian,et al. Wisp2 disruption represses Cxcr4 expression and inhibits BMSCs homing to injured liver[J]. ONCOTARGET,2017,8(58):98823-98836.
APA Qin, Dan.,Yan, Yi.,Hu, Bian.,Zhang, Wanpo.,Li, Hanmin.,...&Zhang, Lisheng.(2017).Wisp2 disruption represses Cxcr4 expression and inhibits BMSCs homing to injured liver.ONCOTARGET,8(58),98823-98836.
MLA Qin, Dan,et al."Wisp2 disruption represses Cxcr4 expression and inhibits BMSCs homing to injured liver".ONCOTARGET 8.58(2017):98823-98836.
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