نتایج جستجو برای: reprogramming

تعداد نتایج: 12767  

Journal: :Cell 2014
Shangqin Guo Xiaoyuan Zi Vincent P. Schulz Jijun Cheng Mei Zhong Sebastian H.J. Koochaki Cynthia M. Megyola Xinghua Pan Kartoosh Heydari Sherman M. Weissman Patrick G. Gallagher Diane S. Krause Rong Fan Jun Lu

Reprogramming somatic cells to induced pluripotency by Yamanaka factors is usually slow and inefficient and is thought to be a stochastic process. We identified a privileged somatic cell state, from which acquisition of pluripotency could occur in a nonstochastic manner. Subsets of murine hematopoietic progenitors are privileged whose progeny cells predominantly adopt the pluripotent fate with ...

2012
Zhonghan Li Tariq M. Rana

Somatic cells can be reprogrammed to form embryonic stem cell-like induced pluripotent stem cells (iPSCs), but the process suffers from low efficiency and the underlying molecular mechanisms that control reprogramming remain poorly understood. Here we perform an inhibitor screen to identify kinases that enhance, or present a barrier to, reprogramming. In particular, inhibitors of p38, inositol ...

Journal: :Cell stem cell 2013
Yawei Gao Jiayu Chen Ke Li Tong Wu Bo Huang Wenqiang Liu Xiaochen Kou Yu Zhang Hua Huang Yonghua Jiang Chao Yao Xiaolei Liu Zhiwei Lu Zijian Xu Lan Kang Jun Chen Hailin Wang Tao Cai Shaorong Gao

DNA methylation and demethylation have been proposed to play an important role in somatic cell reprogramming. Here, we demonstrate that the DNA hydroxylase Tet1 facilitates pluripotent stem cell induction by promoting Oct4 demethylation and reactivation. Moreover, Tet1 (T) can replace Oct4 and initiate somatic cell reprogramming in conjunction with Sox2 (S), Klf4 (K), and c-Myc (M). We establis...

Journal: :Genes & development 2015
Calley L Hirsch Zeynep Coban Akdemir Li Wang Gowtham Jayakumaran Dan Trcka Alexander Weiss J Javier Hernandez Qun Pan Hong Han Xueping Xu Zheng Xia Andrew P Salinger Marenda Wilson Frederick Vizeacoumar Alessandro Datti Wei Li Austin J Cooney Michelle C Barton Benjamin J Blencowe Jeffrey L Wrana Sharon Y R Dent

Embryonic stem cells are maintained in a self-renewing and pluripotent state by multiple regulatory pathways. Pluripotent-specific transcriptional networks are sequentially reactivated as somatic cells reprogram to achieve pluripotency. How epigenetic regulators modulate this process and contribute to somatic cell reprogramming is not clear. Here we performed a functional RNAi screen to identif...

2015
Giacomo Masserdotti Sébastien Gillotin Bernd Sutor Daniela Drechsel Martin Irmler Helle F. Jørgensen Steffen Sass Fabian J. Theis Johannes Beckers Benedikt Berninger François Guillemot Magdalena Götz

Direct lineage reprogramming induces dramatic shifts in cellular identity, employing poorly understood mechanisms. Recently, we demonstrated that expression of Neurog2 or Ascl1 in postnatal mouse astrocytes generates glutamatergic or GABAergic neurons. Here, we take advantage of this model to study dynamics of neuronal cell fate acquisition at the transcriptional level. We found that Neurog2 an...

2015
Nika Shakiba Carl A White Yonatan Y Lipsitz Ayako Yachie-Kinoshita Peter D Tonge Samer M I Hussein Mira C Puri Judith Elbaz James Morrissey-Scoot Mira Li Javier Munoz Marco Benevento Ian M Rogers Jacob H Hanna Albert J R Heck Bernd Wollscheid Andras Nagy Peter W Zandstra

Reprogramming is a dynamic process that can result in multiple pluripotent cell types emerging from divergent paths. Cell surface protein expression is a particularly desirable tool to categorize reprogramming and pluripotency as it enables robust quantification and enrichment of live cells. Here we use cell surface proteomics to interrogate mouse cell reprogramming dynamics and discover CD24 a...

2014
Sophia Kelaini Amy Cochrane Andriana Margariti

The procedure of using mature, fully differentiated cells and inducing them toward other cell types while bypassing an intermediate pluripotent state is termed direct reprogramming. Avoiding the pluripotent stage during cellular conversions can be achieved either through ectopic expression of lineage-specific factors (transdifferentiation) or a direct reprogramming process that involves partial...

Journal: :Cell 2012
Jieun Lee Nazish Sayed Arwen Hunter Kin Fai Au Wing H. Wong Edward S. Mocarski Renee Reijo Pera Eduard Yakubov John P. Cooke

Retroviral overexpression of reprogramming factors (Oct4, Sox2, Klf4, c-Myc) generates induced pluripotent stem cells (iPSCs). However, the integration of foreign DNA could induce genomic dysregulation. Cell-permeant proteins (CPPs) could overcome this limitation. To date, this approach has proved exceedingly inefficient. We discovered a striking difference in the pattern of gene expression ind...

Journal: :Cell systems 2017
Domitilla Del Vecchio Hussein Abdallah Yili Qian James J Collins

To artificially reprogram cell fate, experimentalists manipulate the gene regulatory networks (GRNs) that maintain a cell's phenotype. In practice, reprogramming is often performed by constant overexpression of specific transcription factors (TFs). This process can be unreliable and inefficient. Here, we address this problem by introducing a new approach to reprogramming based on mathematical a...

2017
Francesco Faiola Nuoya Yin Miguel Fidalgo Xin Huang Arven Saunders Junjun Ding Diana Guallar Baoyen Dang Jianlong Wang

Reprogramming somatic cells to induced pluripotent stem cells (iPSCs) is a long and inefficient process. A thorough understanding of the molecular mechanisms underlying reprogramming is paramount for efficient generation and safe application of iPSCs in medicine. While intensive efforts have been devoted to identifying reprogramming facilitators and barriers, a full repertoire of such factors, ...

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