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Scientist Converts Human Skin Cells Into Functional Brain Cells [复制链接]

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楼主
发表于 2011-7-31 22:21 |只看该作者 |倒序浏览 |打印
    A scientist at the Gladstone Institutes has discovered a novel way to convert human skin cells into brain cells, advancing medicine and human health by offering new hope for regenerative medicine and personalized drug discovery and development.- {( ]: C  N; c, `5 G
    In a paper being published online July 28 in the scientific journal Cell Stem Cell, Sheng Ding, PhD, reveals efficient and robust methods for transforming adult skin cells into neurons that are capable of transmitting brain signals, marking one of the first documented experiments for transforming an adult human's skin cells into functioning brain cells./ z: R" h" g  n  x7 _) B% f
    "This work could have important ramifications for patients and families who suffer at the hands of neurodegenerative diseases such Alzheimer's, Parkinson's and Huntington's disease," said Lennart Mucke, MD, who directs neurological research at Gladstone. "Dr. Ding's latest research offers new hope for the process of developing medications for these diseases, as well as for the possibility of cell-replacement therapy to reduce the trauma of millions of people affected by these devastating and irreversible conditions."1 G3 l" b( T+ I5 v9 M
     The work was done in collaboration with Stuart Lipton, M.D., Ph.D., who directs the Del E. Webb Neuroscience, Aging and Stem Cell Research Center at Sanford-Burnham Medical Research Institute. Dr. Ding, one of the world's leading chemical biologists in stem-cell science, earlier this year joined Gladstone and the faculty at the University of California San Francisco (UCSF), as a professor of pharmaceutical chemistry. Gladstone, which is affiliated with UCSF, is a leading and independent biomedical-research organization that is using stem-cell research to advance its work in its three major areas of focus: cardiovascular disease, neurodegenerative disease and viral infections.
6 l+ G9 J/ ]2 C# cDr. Ding's work builds on the cell-reprogramming work of another Gladstone scientist, Senior Investigator Shinya Yamanaka, MD, PhD. Dr. Yamanaka's 2006 discovery of a way to turn adult skin cells into cells that act like embryonic stem cells has radically advanced the fields of cell biology and stem-cell research.: U* t- S) O! K
    Embryonic stem cells -- "pluripotent" cells that can develop into any type of cell in the human body -- hold tremendous promise for regenerative medicine, in which damaged organs and tissues can be replaced or repaired. Many in the science community consider the use of stem cells to be key to the future treatment and eradication of a number of diseases, including heart disease and diabetes. But the use of embryonic stem cells is controversial -- which is one reason why Dr. Yamanaka's discovery of an alternate way to obtain human stem cells, without the use of embryos, is so important.- E/ U! i  m' D; u8 c
    Dr. Ding's work extends Dr. Yamanaka's by offering still another method for avoiding the use of embryonic stem cells and creating an entirely new platform for fundamental studies of human disease. Rather than using models made in yeast, flies or mice for disease research, all cell-reprogramming technology allows human brain, heart and other cells to be created from the skin cells of patients with a specific disease. The new cells created from the skin cells contain a complete set of the genes that resulted in that disease -- representing the potential of a far-superior human model for studying illnesses, drugs and other treatments. In the future, such reprogrammed skin cells could be used to test both drug safety and efficacy for an individual patient with, for example, Alzheimer's disease.
0 w# Z, w* }+ k' H4 C    "This technology should allow us to very rapidly model neurodegenerative diseases in a dish by making nerve cells from individual patients in just a matter of days -- rather than the months required previously," said Dr. Lipton.
2 i. o# E0 P) X$ C( Y    In the experiments being reported July 28, Dr. Ding used two genes and a microRNA to convert a skin sample from a 55-year-old woman directly into brain cells. (MicroRNAs are tiny strands of genetic material that regulate almost every process in every cell of the body.) The cells created by Dr. Ding's experiments exchanged the electrical impulses necessary for brain cells to communicate things such as thoughts and emotions. Using microRNA to reprogram cells is a safer and more efficient way than using the more common gene-modification approach. In ensuing experiments, Dr. Ding hopes to rely only on microRNAs and pharmaceutical compounds to convert skin cells to brain cells, which should lead to more efficient generation of cells for testing and regenerative purposes.
' k4 H0 ^" n* h/ H# l3 m1 L     "This will help us avoid any genome modifications," said Dr. Ding. "These cells are not ready yet for transplantation. But this work removes some of the major technical hurdles to using reprogrammed cells to create transplant-ready cells for a host of diseases."
+ L6 H. K3 ?' o& G% y. s     Dr. Ding is a senior investigator at the Gladstone Institute of Cardiovascular Disease and a UCSF professor of pharmaceutical chemistry. Dr. Ding, who performed the work described in this paper at The Scripps Research Institute, has pioneered the development and application of innovative chemical approaches to stem-cell biology and regeneration.
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沙发
发表于 2011-7-31 22:22 |只看该作者
Rajesh Ambasudhan, Maria Talantova, Ronald Coleman, Xu Yuan, Saiyong Zhu, Stuart A. Lipton, Sheng Ding. Direct Reprogramming of Adult Human Fibroblasts to Functional Neurons under Defined Conditions. Cell Stem Cell, 28 July 2011 DOI: 10.1016/j.stem.2011.07.002

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藤椅
发表于 2011-7-31 22:24 |只看该作者
连发Cell子刊、PNAS文章,丁盛走在干细胞研究的前沿 ' B$ ^5 B/ I2 ]0 R% w% R
【字体:大 中 小】  www.ebiotrade.com  时间:2011年8月1日    来源:生物通
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+ b. i% i% v4 w0 y; S5 D摘要: 近日丁盛博士领导实验室的科研人员在原来的基础上更进一步,他们利用一种新开发的技术绕过iPS阶段成功地将人类皮肤细胞直接转化为了具有信号传导能力的神经元。相关研究论文发表在7月28日的《Cell stem cell》杂志上。  6 n4 Y8 F4 _0 F4 D' i8 S; q1 n! Y

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0 d/ n1 Y7 ~' L' R生物通报道  2006年日本京都大学的山中伸弥博士将4种基因转入小鼠的皮肤纤维细胞,诱导其转化为具有胚胎干细胞样特性的诱导多能干细胞(iPS),为世界上干细胞及再生医学研究开启了新的篇章。利用体细胞重编程获得多能干细胞的方法避免了胚胎干细胞研究存在的伦理争议,并为大规模生产干细胞用于廉价和一致的药物开发铺平了道路。
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: P0 V1 e' c" ~( m# ~: {+ i自从山中伸弥博士用四种转录基因诱导皮肤细胞重编程诱导生成iPS细胞后, 这一技术面临着一个重大缺陷就是插入到细胞的基因会永久性地改变宿主细胞的DNA,此外操作周期长,对许多关键问题认识不深,也使科学家们对iPS技术的风险性提出巨大的质疑。近年来科学家们一直在致力寻找更安全高效的新技术,以获得可广泛适用于再生医学及疾病治疗的安全稳定的细胞。华人科学家丁盛一直走在这一研究领域的前沿,开发了一个完全不同的新方法即利用合成小分子来诱导细胞重编程以及直接转分化。% O2 @' W; b# t! C0 o( G
快速 准确 向猜测说再见,最新Tali™ 成像型多色细胞分析仪,详情请咨询Invitrogen>> >>
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, \) B2 m8 P, u0 i丁盛博士早年毕业于北京大学,现同时受聘于美国斯克里普斯研究所、格拉德斯通心血管病研究所(Gladstone Institute of Cardiovascular Disease)和加州大学旧金山分校,近年来在干细胞研究领域不断取得突破性成果,曾多次在著名干细胞杂志《细胞干细胞》(Cell stem cell)上发表研究论文。
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) ?( u. R; _0 R" |2 ?早在2008年,丁盛实验室就报道发现一些小分子可以替换体细胞重编程中的两个基因。2010年丁盛课题组开发出一种新型的类药小分子连同Oct4基因成功地将人类皮肤细胞重编程为干细胞。这一研究成果发表在《Cell stem cell》杂志上。  o- _8 E  ]# V7 n# l1 i; J
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今年4月,丁盛课题组再度在国际著名期刊《美国科学院院刊》上发表研究论文称他们通过在化学成分确定的培养基中加入一些小分子后成功地诱导人类胚胎干细胞(hESCs)生成了可长期自我更新的原始神经前体细胞,并证实这些神经前体细胞具有定向分化为多种神经元的能力,且不会增高肿瘤形成风险。这一成果标志着研究人员具备了快速生成稳定可更新的神经干细胞及下游产品的能力,从而确保能获得大量临床数量级的干细胞(一周超过100万个细胞)用于临床实验,并最终运用到临床治疗中。
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  [2 L, G( i, C. L2 G: A# U近日丁盛博士领导实验室的科研人员在原来的基础上更进一步,他们利用一种新开发的技术绕过iPS阶段成功地将人类皮肤细胞直接转化为了具有信号传导能力的神经元。相关研究论文发表在7月28日的《Cell stem cell》杂志上。
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在这篇文章中,研究人员通过在化学成分确定的培养基中加入一种miRNA(miR-124)与两个转录因子(MYT1L and BRN2)的方法成功地将新生儿及成人原代皮肤成纤维细胞直接转化为功能性的神经元。这些人类诱导神经元细胞(hiNs)不仅显示典型的神经元形态,表达多种神经元标志蛋白。并且能够产生动作电位,相互之间形成神经突触并传导信号。9 b! v" u# s. G3 |( ~- o* E0 N

% T: e0 K- W! C1 p" D6 q丁盛博士的合作者、斯坦福医学研究所的Stuart A. Lipton博士说:“这一新技术使得研究人员能够利用患者自身细胞在培养皿中快速构建出神经变性疾病模型。相比于过去长达数月的周期,这一过程仅需要数日的时间,”
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0 A/ V0 Y; _2 x* t9 } “这一研究对于那些遭受神经变性疾病例如阿尔茨海默病、帕金森氏病和亨廷顿舞蹈病等疾病的患者及家庭无疑具有重要的意义,”美国格拉德斯通神经学研究负责人Lennart Mucke博士表示:“丁博士的最新研究为他们带来了新希望,表明通过细胞替代疗法利用患者自身的细胞生成新细胞替代那些疾病或损伤的细胞,将使那些目前医学上束手无策的疑难疾病的治疗变为可能。”- X( q" {% z, z4 g; j5 w6 [

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  W/ C/ v, Z3 k+ L9 H" n1 H生物通推荐原文摘要:
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& ~& ?; H  y- X8 Y/ WDirect Reprogramming of Adult Human Fibroblasts to Functional Neurons under Defined Conditions
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Human induced pluripotent stem cells (hiPSCs) have been generated by reprogramming a number of different somatic cell types using a variety of approaches. In addition, direct reprogramming of mature cells from one lineage to another has emerged recently as an alternative strategy for generating cell types of interest. Here we show that a combination of a microRNA (miR-124) and two transcription factors (MYT1L and BRN2) is sufficient to directly reprogram postnatal and adult human primary dermal fibroblasts (mesoderm) to functional neurons (ectoderm) under precisely defined conditions. These human induced neurons (hiNs) exhibit typical neuronal morphology and marker gene expression, fire action potentials, and produce functional synapses between each other. Our findings have major implications for cell-replacement strategies in neurodegenerative diseases, disease modeling, and neural developmental studies.
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板凳
发表于 2011-7-31 22:25 |只看该作者
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