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
2009年
49期
9739-9742
,共4页
干细胞%运动神经元%分化%综述文献
榦細胞%運動神經元%分化%綜述文獻
간세포%운동신경원%분화%종술문헌
目前研究证明胚胎干细胞和神经干细胞可以诱导分化为运动神经元,诱导主要方法是在培养过程中加入诱导因子,从而提高分化培养中运动神经元的分化比例.运动神经元在体外培养中发育成熟的过程与其在胚胎内发育过程类似,也有Pax6、Nkx6.1、Olig2和HB9等转录因子的参与,其中以HB9为分选标志的细胞在体外几乎完全分化为运动神经元.此外,还有其他种类的蛋白标志用到运动神经元的诱导分化鉴定中,如神经元标志MAP-2、β-tubulin-Ⅲ,胆碱能细胞标志ChAT、VAChT,许旺细胞有丝分裂原REG2,电压依赖性钙离子通道亚单位等.运动神经元诱导分化的鉴定除了上述特异性分子标志表达的检测外,还需检验分化的运动神经元是否具有功能.运动神经元功能的检测方法可分为两类,一是检测体外培养中的运动神经元是否具有功能,二是检测分化的运动神经元移植到动物体内是否也同样具有功能.干细胞诱导分化为运动神经元方法已基本成熟,但距临床应用还有很多问题需要进一步讨论,如关于运动神经元诱导分化的细胞来源、运动神经元诱导分化的效率、分化运动神经元的纯化、运动神经元的功能等.
目前研究證明胚胎榦細胞和神經榦細胞可以誘導分化為運動神經元,誘導主要方法是在培養過程中加入誘導因子,從而提高分化培養中運動神經元的分化比例.運動神經元在體外培養中髮育成熟的過程與其在胚胎內髮育過程類似,也有Pax6、Nkx6.1、Olig2和HB9等轉錄因子的參與,其中以HB9為分選標誌的細胞在體外幾乎完全分化為運動神經元.此外,還有其他種類的蛋白標誌用到運動神經元的誘導分化鑒定中,如神經元標誌MAP-2、β-tubulin-Ⅲ,膽堿能細胞標誌ChAT、VAChT,許旺細胞有絲分裂原REG2,電壓依賴性鈣離子通道亞單位等.運動神經元誘導分化的鑒定除瞭上述特異性分子標誌錶達的檢測外,還需檢驗分化的運動神經元是否具有功能.運動神經元功能的檢測方法可分為兩類,一是檢測體外培養中的運動神經元是否具有功能,二是檢測分化的運動神經元移植到動物體內是否也同樣具有功能.榦細胞誘導分化為運動神經元方法已基本成熟,但距臨床應用還有很多問題需要進一步討論,如關于運動神經元誘導分化的細胞來源、運動神經元誘導分化的效率、分化運動神經元的純化、運動神經元的功能等.
목전연구증명배태간세포화신경간세포가이유도분화위운동신경원,유도주요방법시재배양과정중가입유도인자,종이제고분화배양중운동신경원적분화비례.운동신경원재체외배양중발육성숙적과정여기재배태내발육과정유사,야유Pax6、Nkx6.1、Olig2화HB9등전록인자적삼여,기중이HB9위분선표지적세포재체외궤호완전분화위운동신경원.차외,환유기타충류적단백표지용도운동신경원적유도분화감정중,여신경원표지MAP-2、β-tubulin-Ⅲ,담감능세포표지ChAT、VAChT,허왕세포유사분렬원REG2,전압의뢰성개리자통도아단위등.운동신경원유도분화적감정제료상술특이성분자표지표체적검측외,환수검험분화적운동신경원시부구유공능.운동신경원공능적검측방법가분위량류,일시검측체외배양중적운동신경원시부구유공능,이시검측분화적운동신경원이식도동물체내시부야동양구유공능.간세포유도분화위운동신경원방법이기본성숙,단거림상응용환유흔다문제수요진일보토론,여관우운동신경원유도분화적세포래원、운동신경원유도분화적효솔、분화운동신경원적순화、운동신경원적공능등.
Studies have shown that embryonic stem cells and neural stem ceils could be induced to differentiate into motor neurons by adding inducing factors to the culture to improve differentiation proportion of motor neurons. The development and maturation process of motor neurons in vitro culture is similar to that in embryo, involving participation of Pax6, Nk×6.1, Olig2 and HB9. Moreover, cells with HB9 as separation mark almost differentiate into motor neurons in vitro. In addition, other types of protein marks have been used for identification of motor neuronal induced differentiation, such as neuron mark MAP-2, β-tubulin-Ⅲ, cholinergic cell mark ChAT, VAChT, Schwann cell mitogen REG2, and voltage-dependent calcium ion channel 11.2 subunit. The identification of induced differentiation of motor neurons also involves detection of function of differentiated motor neurons by two methods. One method is to detect the function of in vitro cultured motor neurons, and the other is to detect the function of transplanted motor neurons in vivo. Although induced differentiation of stem cells into motor neurons becomes mature, many issues remain in clinical application, such as cell sources of induced differentiation of motor neuron, efficiency of induced differentiation, purification of differentiated motor neurons, and function of motor neurons.