The Development of Spermatogonial Stem Cells andTheir Pluripotency

来源 :第十四次全国医学遗传学学术会议 | 被引量 : 0次 | 上传用户:you3880066
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
  Spermatogonial stem cells (SSCs) , also known as male germline stem cells, are one of the most important stem cell systems throughout the life of male animals, not only because they are the unique adult stem cells that transmit genetic information to offspring, but also the potential pluripotency that they indicated in recent studies.However, the mechanism of its pluripotency remains poorly understood.In this review, we focused on discussing the approaches for isolation and purification SSCs as well as cultivation and identification SSCs.Based on the published studies, the unlimited potential of SSCs to acquire pluripotency and plasticity under specific culture conditions were discussed as well.Meanwhile, we addressed therapeutic potential and potential future utility of SSCs in both human reproductive and regenerative medicine.Furthermore, SSCs.may also provide new opportunities to study genetic diseases in various cell lineages in the future.
其他文献
  目的:对1例疑似Leigh综合征(LS)患者行相关基因微小突变分析.方法:采用外显子组测序分析(exome sequencing analysis)对患者行线粒体及线粒体相关核基因筛查,再Sanger测序进
会议
  目的:了解中国南方Prader-Willi综合征(PWS)患儿临床表现及分子特征,为临床筛查和进一步行分子诊断提供依据.方法:分析2012年11月至2014年11月于广州市妇女儿童医疗中心经
会议
  Aims: Limb-girdle muscular dystrophy type 2A (LGMD2A) is an autosomal recessive disorder characterized by symmetrical and selective atrophy of the proximal
会议
  Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder characterized by hamartomas in multiple organ systems.It is caused by inactivatin
会议
  目的:对一个视网膜色素变性(Retinitis pigmentosa)的家系进行相关基因突变检测,以明确该家系病因及家系成员基因型.方法:采集先证者外周血,通过目标序列芯片捕获高通量测
会议
目的:对一个先天性软骨发育不全(achondroplasia,ACH)家系的先证者及所怀胎儿进行成纤维细胞生长因子受体3(Fibroblast growthfactorreceptor 3,FGFR3)基因突变分析。方法:抽
  Approximately 30% of pregnancies after implantation end up in spontaneous abortions, and 50% of them are caused by chromosomal abnormalities.ondly aCGH for
会议
  目的:对一例临床表现为骨骼发育异常(Skeletal Dysplasia)的患者进行相关基因突变分析,以明确诊断。方法:采集患者外周血,通过芯片捕获高通量测序技术,对FGFR3、CLCN7、COL1A1
会议
  Gaucher's disease (GD)is an autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (glucocerebrosidase) that results in the accumulati
会议
  目的:研究癌-睾丸抗原PlWl蛋白家族成员Piwil1和Piwil2在肿瘤细胞中的作用及其调控机制。方法:通过构建PlWl蛋白家族成员Piwil1和Piwil2的真核表达载体和shRNA干扰载体等载
会议