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Wnt 신호전달 조절인자인 sFRP1의 인간 골수유래 중간엽 줄기세포의 증식 조절기작에 관한 연구
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.advisor | 서해영, 김성수, 이영돈 | - |
| dc.contributor.author | Lee Na Ra | - |
| dc.date.accessioned | 2019-10-21T07:26:50Z | - |
| dc.date.available | 2019-10-21T07:26:50Z | - |
| dc.date.issued | 2016-02 | - |
| dc.identifier.other | 21819 | - |
| dc.identifier.uri | https://dspace.ajou.ac.kr/handle/2018.oak/18799 | - |
| dc.description | 학위논문(석사)--아주대학교 일반대학원 :의생명과학과,2016. 2 | - |
| dc.description.tableofcontents | INTRODUCTION 1 MATERIALS AND METHODS 6 Culture of human MSCs in vitro 6 Differentiation of human MSCs in vitro 6 SA-β-gal staining 7 Semiquantitative - (RT-PCR) and quantitative-reverse transcriptase polymerase chain reaction (qRT-PCR) 7 Production of virus and Transduction 8 Growth kinetics of hMSCs 8 Treatment of recombinant human sFRP1 protein 9 Immunocytochemistry 9 Western blot analysis 9 RESULTS 11 DISCUSSION 24 REFERENCES 27 국문요약 35 | - |
| dc.language.iso | eng | - |
| dc.publisher | The Graduate School, Ajou University | - |
| dc.rights | 아주대학교 논문은 저작권에 의해 보호받습니다. | - |
| dc.title | Wnt 신호전달 조절인자인 sFRP1의 인간 골수유래 중간엽 줄기세포의 증식 조절기작에 관한 연구 | - |
| dc.title.alternative | Control of proliferation in human mesenchymal stem cells by Secreted Frizzled Related Protein 1 | - |
| dc.type | Thesis | - |
| dc.contributor.affiliation | 아주대학교 일반대학원 | - |
| dc.contributor.department | 일반대학원 의생명과학과 | - |
| dc.date.awarded | 2016. 2 | - |
| dc.description.degree | Master | - |
| dc.identifier.localId | 739463 | - |
| dc.identifier.url | http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021819 | - |
| dc.subject.keyword | sFRP1 | - |
| dc.description.alternativeAbstract | Human mesenchymal stem cell (hMSC) is adult stem cell that is useful tool for a various disease. However, it has limitations that lost proliferation and differentiation ability in long-term in vitro culture and occurred senescence. This study would like to confirm the relationship between Wnt signaling and proliferation of hMSCs. When checked mRNA expression of various genes that were related to Wnt signaling, most of genes were decreased gradually as follow passages, except Wnt11. Especially, gene expression of sFRP1, an antagonist of Wnt signaling, was also decreased. To confirm whether sFRP1 affects proliferation of hMSC, MSC/sFRP1 and MSC/shsFRP1 were made and then cell proliferation was measured. Growth kinetics result showed that sFRP1 could affect hMSCs’ proliferation and this could be dependent on concentration. Meanwhile, Wnt signaling can be divided into canonical and non-canonical pathway depending on beta-catenin involvement in the pathway. RORα is down-stream gene of non-canonical Wnt pathway and it could be translocated into nucleus to interact with β-catenin, resulting in suppression of cell proliferation. This study confirmed that RORα expression and nuclear translocation were increased in late passage of hMSCs. Also, MSC/shRORα showed promoted growth kinetics, indicating that RORα could be a negative regulator of hMSCs’ proliferation. To figure out whether sFRP1 inhibits nuclear translocation of RORα to suppress non-canonical Wnt signaling, 10ng/ml sFRP1 was treated to hMSCs and localization of RORα was observed. ICC data showed that nuclear translocation of RORα was inhibited in rhsFRP1 treated hMSCs, suggesting that sFRP1 promotes hMSCs’ proliferation by suppressing non-canonical Wnt signaling | - |
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- Graduate School of Ajou University > Department of Biomedical Sciences > 3. Theses(Master)
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