Abstract:
:The discovery of the Ten-Eleven Translocation (TET) protein family was initiated by the identification of the MLL partner TET1, and of mutations in the TET2 gene in hematological malignancies including myeloproliferative neoplasms (MPN). TET1, 2 and 3 proteins hydroxylate 5-methylcytosine (5-mC) into 5-hydroxymethylcytosine (5-hmC) and further oxidize 5-hmC into 5-formylcytosine (5-fC) and 5-carboxylcytosine (5-caC). Previous studies highlight the involvement of TET proteins in somatic cells reprogramming into induced pluripotent stem cells (iPSC), particularly Tet1 and 2 in mouse and TET1 in human. Here, we asked whether endogenous TET2 knockdown also displays this function. Using different shRNA against TET2, we provide evidence that TET2 strongly decreases the reprogramming of human hematopoietic progenitor cells into iPSC. Importantly, using 2 MPN patients, we observed that TET2 mutations affecting catalytic domain allowed iPSC generation. Instead, using another TET2 and TET3-mutated patient, we could only reprogram IPSC with TET3 mutation alone, suggesting that the type of TET2 mutation and/or the cooperation with TET3 mutations may alter the reprogramming activity. Altogether, this work highlights the importance of endogenous TET in the reprogramming process of human hematopoietic progenitors.
journal_name
Stem Cell Resjournal_title
Stem cell researchauthors
Secardin L,Limia CEG,di Stefano A,Bonamino MH,Saliba J,Kataoka K,Rehen SK,Raslova H,Marty C,Ogawa S,Vainchenker W,Monte-Mor BDCR,Plo Idoi
10.1016/j.scr.2020.101755subject
Has Abstractpub_date
2020-04-01 00:00:00pages
101755eissn
1873-5061issn
1876-7753pii
S1873-5061(20)30059-3journal_volume
44pub_type
杂志文章abstract::Incomplete achromatopsia (ACHM) is a disorder in which there is function defect of cone photoreceptors in the retina and individuals with such disease retain residual color vision. Here, we have generated an induced pluripotent stem cell (iPSC) line carrying a homozygous mutation in the PDE6C gene, already related wit...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101569
更新日期:2019-10-01 00:00:00
abstract::The KCL037 human embryonic stem cell line was derived from a normal healthy blastocyst donated for research. The ICM was isolated using laser microsurgery and plated on γ-irradiated human foreskin fibroblasts. Both the derivation and cell line propagation were performed in an animal product-free environment and under ...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2015.12.023
更新日期:2016-01-01 00:00:00
abstract::Induced pluripotent stem cells (iPSCs) were generated from peripheral blood mononuclear cells (PBMCs) obtained from a 60-year-old female diagnosed with sporadic amyotrophic lateral sclerosis (sALS). The iPSCs shared the same karyotype with the parent PBMCs, expressed pluripotency stem cell markers, and demonstrated tr...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.101841
更新日期:2020-05-01 00:00:00
abstract:BACKGROUND:Angiogenesis is an essential step in tissue engineering. MSC exosomes play an important role in angiogenesis. Functional biomolecules in exosomes vested by the culture microenvironment can be transferred to recipient cells and affects their effect. 3D culture can improve the proliferation and activity of MSC...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.102122
更新日期:2020-12-10 00:00:00
abstract::Autism is a heterogeneous neurodevelopmental disorder defined by deficits in socialization, communication, and patterns of behavior. Using stem cells to model brain disordersmay yield new understanding about the underlying neuropathological processes and could prove essential for drug development. We present here a ne...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.102038
更新日期:2020-12-01 00:00:00
abstract::Two distinct types of embryonic pluripotent stem cells can be established from either the inner cell mass (ICM) of preimplantation blastocyst (leukemia inhibitory factor (LIF)-dependent embryonic stem cell, ESC, called naive state) or the epiblast of postimplantation fetuses (fibroblast growth factor 2 (FGF2)-dependen...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2014.04.012
更新日期:2014-07-01 00:00:00
abstract::Neuroblasts represent the predominant migrating cell type in the adult mouse brain. There are, however, increasing evidences of migration of other neural precursors. This work aims at identifying in vivo endogenous early neural precursors, different from neuroblasts, able to migrate in response to brain injuries. The ...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2014.11.006
更新日期:2015-01-01 00:00:00
abstract::Ectopic expression of HoxB4 in embryonic stem (ES) cells leads to an efficient production of hematopoietic cells, including hematopoietic stem/progenitor cells. Previous studies have utilized a constitutive HoxB4 expression system or tetracycline-regulated HoxB4 expression system to induce hematopoietic cells from ES ...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2011.09.001
更新日期:2012-03-01 00:00:00
abstract::Skin fibroblasts were obtained from four patients with Williams-Beuren syndrome (WBS) carrying the typical 1.5 Mb or 1.8 Mb deletion at the 7q11.23 genomic region. Induced pluripotent stem cells (iPSCs) were generated by retroviral infection of fibroblasts with polycystronic vectors. The generated iPSC clones ESi059A,...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.102087
更新日期:2020-12-01 00:00:00
abstract::The Mesenchymal-to-Epithelial Transition (MET) has been recognized as a crucial step for successful reprogramming of fibroblasts to induced pluripotent stem cells (iPSCs). Thus, it has been demonstrated, that the efficiency of reprogramming can be enhanced by promoting an epithelial expression program in cells, with a...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2014.11.003
更新日期:2015-01-01 00:00:00
abstract::SOX4 has been shown to promote neuronal differentiation both in the adult and embryonic neural progenitors. Ectopic SOX4 expression has also been shown to inhibit oligodendrocyte differentiation in mice, however the underlying molecular mechanisms remain poorly understood. Here we demonstrate that SOX4 regulates trans...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2018.10.005
更新日期:2018-12-01 00:00:00
abstract::To develop a disease model for the human 'brittle bone' disease, osteogenesis imperfecta, we have used gene editing to produce a facsimile of the patient heterozygous COL1A1 mutation in an established control iPSC line. The gene-edited line had a normal karyotype, expressed pluripotency markers and differentiated into...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101449
更新日期:2019-05-01 00:00:00
abstract::The Genea079 human embryonic stem cell line was derived from a donated, fully commercially consented ART blastocyst, carrying compound heterozygous mutations in the NEB gene, exon 55 deletion & c.15110dupA, indicative of Nemaline Myopathy Type 2 (NEM2). Following ICM outgrowth on inactivated human feeders, karyotype w...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2016.02.015
更新日期:2016-03-01 00:00:00
abstract::Human skin fibroblasts were isolated from a 40-year-old hereditary spastic paraplegia patient carrying an intronic splice site mutation (c.1687+2T>A) in SPAST, leading to hereditary spastic paraplegia type 4 (SPG4). Fibroblasts were reprogrammed using episomal plasmids carrying hOCT4, hSOX2, hKLF4, hL-MYC and hLIN28. ...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2016.09.022
更新日期:2016-11-01 00:00:00
abstract::The human embryonic stem cell line RCe019-A (RC-15) was derived under quality assured compliance with UK regulation, European Union Directives and International guidance for tissue procurement, processing and storage according to Good Manufacturing Practice (GMP) standards. The cell line was derived from a cleavage st...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2016.04.003
更新日期:2016-05-01 00:00:00
abstract::A skin biopsy was obtained from a 14-year-old female patient with a history of Myelomeningocele. Dermal fibroblasts were isolated and reprogrammed with Sendai virus (SeV) vectors encoding OCT3/4, SOX2, KLF4, and c-MYC. The generated induced Pluripotent Stem Cell (iPSC) clones NTDi4_09A were free of genomically integra...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2018.05.007
更新日期:2018-08-01 00:00:00
abstract::Cell-mediated gene therapy is a possible means to treat muscular dystrophies like Duchenne muscular dystrophy. Autologous patient stem cells can be genetically-corrected and transplanted back into the patient, without causing immunorejection problems. Regenerated muscle fibres derived from these cells will express the...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2018.05.004
更新日期:2018-07-01 00:00:00
abstract::Optimization of pluripotent stem cell expansion and differentiation is facilitated by biological tools that permit non-invasive and dynamic monitoring of pluripotency, and the ability to select for an undifferentiated input cell population. Here we report on the generation and characterisation of clonal human embryoni...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2014.05.006
更新日期:2014-09-01 00:00:00
abstract::Primary hyperoxaluria type 1 (PH1) is a rare autosomal recessive disorder of the liver metabolism due to functional deficiency of the peroxisomal enzyme alanine:glyoxylate aminotransferase (AGT). AGT deficiency results in overproduction of oxalate which complexes with calcium to form insoluble calcium-oxalate salts in...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101467
更新日期:2019-07-01 00:00:00
abstract::Neural stem cells (NSCs) have been considered as potential therapy in Alzheimer's disease (AD) but their use is hampered by the poor survival of grafted cells. Supply of neurotrophic factors to the grafted cells has been proposed as a way to augment survival of the stem cells. In this context, we investigated the util...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2015.04.008
更新日期:2015-07-01 00:00:00
abstract::Peripheral blood mononuclear cells (PBMCs) were collected from a 6-year-old female child who was clinically diagnosed as primary nephrotic syndrome (NS) with hormone resistance. An iPSC line was successfully established by the Sendai-virus (SeV) delivery system. The iPS-19 (GSPHi001-A) expressed pluripotent markers, e...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101661
更新日期:2019-12-01 00:00:00
abstract::Our work aimed at evaluating the role of adipose stem cells (ASC) on chondrocytes from osteoarthritic (OA) patients and identifying the mediators involved. We used primary chondrocytes, ASCs from different sources and bone marrow mesenchymal stromal cells (MSC) from OA donors. ASCs or MSCs were co-cultured with chondr...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2013.05.008
更新日期:2013-09-01 00:00:00
abstract::Human iPSC line N44SV.5 was generated from primary normal human dermal fibroblasts belonging to the European mitochondrial haplogroup U. For this purpose, reprogramming factors Oct3/4, Sox2, Klf4, and cMyc were delivered using a non-integrative methodology that involves the use of Sendai virus. ...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2015.12.010
更新日期:2016-01-01 00:00:00
abstract::Human FOXH1 (Forkhead Box H1) gene encodes a human homolog of Xenopus forkhead activing signal transducer-1 and has been shown to play an important role in mesendoderm formation in X. tropicalis and mice. However, little is known about the function of FOXH1 in human development. Here we generated a FOXH1 homozygous kn...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.102121
更新日期:2020-12-10 00:00:00
abstract::Loeys-Dietz syndrome (LDS) is a rare connective tissue disorder characterized by a genetic predisposition for thoracic aortic aneurysm and dissection. Despite heterozygous loss-of-function mutations in genes for ligand, receptor, or downstream mediators of the transforming growth factor β (TGFβ) pathway, LDS is associ...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.101707
更新日期:2020-03-01 00:00:00
abstract::We report here a transgenic murine induced pluripotent stem cell (iPSC) line expressing puromycin N-acetyltransferase (PAC) and enhanced green fluorescent protein (EGFP) under the control of α-myosin heavy chain promoter. This transgenic cell line reproducibly differentiates into EGFP-expressing cardiomyocytes (CMs) w...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2016.07.007
更新日期:2016-09-01 00:00:00
abstract::The cell surface protein Stem Cell Antigen-1 (Sca-1) marks stem or progenitor cells in several murine tissues and is normally upregulated during cancer development. Although the specific function of Sca-1 remains unknown, Sca-1 seems to play a role in proliferation, differentiation and cell migration in a number of ti...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2017.07.002
更新日期:2017-08-01 00:00:00
abstract::The peptide hormone insulin produced by pancreatic β-cells undergoes post-transcriptional processing before secretion. In particular, C-peptide is cleaved from pro-insulin to generate mature insulin. Here, we introduce a C-peptide-mCherry human iPSC line (HMGUi001-A-8). The line was generated by CRISPR/Cas9 mediated h...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.102126
更新日期:2020-12-16 00:00:00
abstract::Human embryonic stem cells (hESCs) can undergo unlimited self-renewal and differentiate into hepatic cells, including expandable hepato-blasts (HBs) and hepatocyte-like cells (HLCs) in vitro. Therefore, hESC-derived HBs have the potential to become a renewable cell source for cell therapy of serious liver damage. Howe...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.102010
更新日期:2020-12-01 00:00:00
abstract::Progenitor cells in the adult pancreas are potential sources of endocrine beta cells for treating type 1 diabetes. Previously, we identified tri-potent progenitor cells in the adult (2-4month-old) murine pancreas that were capable of self-renewal and differentiation into duct, acinar, and endocrine cells in vitro. The...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2015.11.015
更新日期:2016-01-01 00:00:00