中国组织工程研究与临床康复
中國組織工程研究與臨床康複
중국조직공정연구여림상강복
JOURNAL OF CLINICAL REHABILITATIVE TISSUE ENGINEERING RESEARCH
2010年
6期
1084-1087
,共4页
信号分子%HSC%Wnt%Notch%Bmi_1%Shh%HOXB4%造血干细胞
信號分子%HSC%Wnt%Notch%Bmi_1%Shh%HOXB4%造血榦細胞
신호분자%HSC%Wnt%Notch%Bmi_1%Shh%HOXB4%조혈간세포
背景:造血干细胞数目少,且在体外容易分化,这对其应用于移植存在很大的困难.目的:文章集中阐述了Wnt、Notch、Bmi_1、Shh、HOXB4信号分子在维持造血干细胞自我更新调控中的作用及其途径.方法:以HSC、Wnt、Notch、Bmi_1、Shh、HOXB4为检索词,检索PubMed数据库(2002-01/2008-12).文献检索语种限制为英文.纳入与造血干细胞自我更新相关信号分子密切相关的文献.排除重复性研究和Meta分析.结果与结论:计算机初步检索到216篇文献,对其中30篇文献进行研究.造血干细胞是具有自我更新、较强分化发育和再生能力、可以产生各种类型血细胞的始祖细胞,被广泛应用于治疗血液系统疾病,但是造血干细胞在体外容易分化,这对其应用于移植存在很大的困难.如何使造血干细胞在体外扩增和处理的同时保持造血干细胞的自我更新特性成为关键问题.近年来通过不同信号通路增强造血干细胞自我更新能力的信号分子成为研究热点.文章集中阐述了Wnt、Notch、Bmi_1、Shh、HOXB4在维持造血干细胞自我更新调控中的作用及其途径,发现上述5种信号分子均具有增强造血干细胞自我更新的功能.此外还有一些因素在维持造血干细胞自我更新的过程中起重要作用,如作为内源性因素的一系列转录因子Oct-4、Ehox、Nanog、SCL、Runx1等,探讨它们相互作用形成的调控网络如何调控造血干细胞的自我更新,将成为造血干细胞自我更新领域研究的一个重点.
揹景:造血榦細胞數目少,且在體外容易分化,這對其應用于移植存在很大的睏難.目的:文章集中闡述瞭Wnt、Notch、Bmi_1、Shh、HOXB4信號分子在維持造血榦細胞自我更新調控中的作用及其途徑.方法:以HSC、Wnt、Notch、Bmi_1、Shh、HOXB4為檢索詞,檢索PubMed數據庫(2002-01/2008-12).文獻檢索語種限製為英文.納入與造血榦細胞自我更新相關信號分子密切相關的文獻.排除重複性研究和Meta分析.結果與結論:計算機初步檢索到216篇文獻,對其中30篇文獻進行研究.造血榦細胞是具有自我更新、較彊分化髮育和再生能力、可以產生各種類型血細胞的始祖細胞,被廣汎應用于治療血液繫統疾病,但是造血榦細胞在體外容易分化,這對其應用于移植存在很大的睏難.如何使造血榦細胞在體外擴增和處理的同時保持造血榦細胞的自我更新特性成為關鍵問題.近年來通過不同信號通路增彊造血榦細胞自我更新能力的信號分子成為研究熱點.文章集中闡述瞭Wnt、Notch、Bmi_1、Shh、HOXB4在維持造血榦細胞自我更新調控中的作用及其途徑,髮現上述5種信號分子均具有增彊造血榦細胞自我更新的功能.此外還有一些因素在維持造血榦細胞自我更新的過程中起重要作用,如作為內源性因素的一繫列轉錄因子Oct-4、Ehox、Nanog、SCL、Runx1等,探討它們相互作用形成的調控網絡如何調控造血榦細胞的自我更新,將成為造血榦細胞自我更新領域研究的一箇重點.
배경:조혈간세포수목소,차재체외용역분화,저대기응용우이식존재흔대적곤난.목적:문장집중천술료Wnt、Notch、Bmi_1、Shh、HOXB4신호분자재유지조혈간세포자아경신조공중적작용급기도경.방법:이HSC、Wnt、Notch、Bmi_1、Shh、HOXB4위검색사,검색PubMed수거고(2002-01/2008-12).문헌검색어충한제위영문.납입여조혈간세포자아경신상관신호분자밀절상관적문헌.배제중복성연구화Meta분석.결과여결론:계산궤초보검색도216편문헌,대기중30편문헌진행연구.조혈간세포시구유자아경신、교강분화발육화재생능력、가이산생각충류형혈세포적시조세포,피엄범응용우치료혈액계통질병,단시조혈간세포재체외용역분화,저대기응용우이식존재흔대적곤난.여하사조혈간세포재체외확증화처리적동시보지조혈간세포적자아경신특성성위관건문제.근년래통과불동신호통로증강조혈간세포자아경신능력적신호분자성위연구열점.문장집중천술료Wnt、Notch、Bmi_1、Shh、HOXB4재유지조혈간세포자아경신조공중적작용급기도경,발현상술5충신호분자균구유증강조혈간세포자아경신적공능.차외환유일사인소재유지조혈간세포자아경신적과정중기중요작용,여작위내원성인소적일계렬전록인자Oct-4、Ehox、Nanog、SCL、Runx1등,탐토타문상호작용형성적조공망락여하조공조혈간세포적자아경신,장성위조혈간세포자아경신영역연구적일개중점.
BACKGROUND: There are small amount of hematopoietic stem cells, which are easy to divide in vitro and show the difficulty in applying to transplantation.OBJECTIVE: This paper has focused on the role and means of the Wnt, Notch, Bmi_1, Shh, HOXB4 signaling molecule in the maintenance of hematopoietic stem cell self-renewal and regulation. METHODS: With the key words of "HSC, Wnt, Notch, Bmi_1, Shh, HOXB4" for the search, we searched PubMed database (2002-01/2008-12) in English. Literatures closely related to the hematopoietic stem cell self-renewal related signaling molecules were included. Repetitive research and Meta analysis were excluded.RESULTS AND CONCLUSION: The computer initially retrieved 216 documents, of which 30 documents for research. Hematopoietic stem cells are self-renewing, have strong differentiation and growth and regeneration capacities, can produce various types of blood cells ancestor cells, are widely used to treat blood diseases, but the hematopoietic stem cell differentiation in vitro demonstrated that the difficulties used in transplantation. How to make hematopoietic stem cells in vitro amplification and processing, while maintaining hematopoietic stem cell self-renewal characteristics is of a key issue. In recent years, different signaling pathways to enhance the ability of hematopoietic stem cell self-renewal signaling molecule have been a research hotspot. The article focused on the role and means of the Wnt, Notch, Bmi_1, Shh, HOXB4 in the maintenance of hematopoietic stem cell self-renewal and regulation and found that both the above-mentioned five signaling molecules can enhance hematopoietic stem cell self-renewal function. There are also a number of factors playing an important role in the maintenance of hematopoietic stem cell self-renewal process, such as endogenous factors, a series of transcription factors Oct-4, Ehox, Nanog, SCL, Runx1 and so on, to explore how their regulatory networks formed by the interaction control self-renewal of hematopoietic stem cells will become a key point in the research of self-renewal of hematopoietic stem cells.