Abstract:
:Urine resource cells were collected from a 23-year-old male with multiple endocrine neoplasia type 1 syndrome (MEN1) for generating iPS cells with episomal plasmids. Two stable iPSC lines with free of episomal plasmid were established. The patient has a heterozygous G>T mutation on the exon 9 of Men1 gene that was confirmed by sequencing analysis on all resulted cell lines. Karyotyping indicated the chromosomes with normal appearances and numbers. Their pluripotency was demonstrated by gene expression and their abilities for differentiating into three germ layers. These iPSC lines provide valuable in vitro resources for pathological study on MEN1 syndrome.
journal_name
Stem Cell Resjournal_title
Stem cell researchauthors
Guo D,Wu F,Liu H,Gao G,Kou S,Yang F,Abbas N,Zhou T,Cai X,Zhang H,Qin D,Li J,Xu K,Li YXdoi
10.1016/j.scr.2016.12.002subject
Has Abstractpub_date
2017-01-01 00:00:00pages
70-72eissn
1873-5061issn
1876-7753pii
S1873-5061(16)30202-1journal_volume
18pub_type
杂志文章abstract::We describe the generation and characterization of 5 human induced pluripotent stem cell (iPSC) lines derived from peripheral blood mononuclear cells (PBMCs) of healthy adult individuals. The PBMCs were reprogrammed using non-integrating Sendai viruses containing the reprogramming factors POU5F1 (OCT4), SOX2, KLF4 and...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2018.101380
更新日期:2019-01-01 00:00:00
abstract::An 83-year old Alzheimer's disease (AD) male patient donated his Peripheral blood mononuclear cells (PBMC). The non-integrating episomal vector system used to reprogram PBMCs with the human OKSM transcription factors. The pluripotency of transgene-free iPSCs was confirmed by immunocytochemistry for pluripotency marker...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2018.11.008
更新日期:2018-12-01 00:00:00
abstract::Spinocerebellar ataxia type 3 (SCA3) is a dominantly inherited neurodegenerative disease caused by a CAG-repeat expanding mutation in ATXN3. We generated induced pluripotent stem cells (iPSCs) from a SCA3 patient by electroporation of dermal fibroblasts with episomal plasmids encoding L-MYC, LIN28, SOX2, KLF4, OCT4 an...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2016.02.040
更新日期:2016-05-01 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::Endothelial progenitor cells (EPCs) may contribute to neurovascular repair after stroke and neurodegeneration. A key step in this process should involve adhesive interactions between EPCs and the targeted cerebral endothelium. Here, we tested the hypothesis that reactive astrocytes may play a critical role in enhancin...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2013.12.008
更新日期:2014-03-01 00:00:00
abstract::Salisphere-derived adult epithelial cells have been used to improve saliva production of irradiated mouse salivary glands. Importantly, optimization of the cellular composition of salispheres could improve their regenerative capabilities. The Rho Kinase (ROCK) inhibitor, Y27632, has been used to increase the prolifera...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101608
更新日期:2019-12-01 00:00:00
abstract::The human iPSC cell line, CARS-FiPS4F1 (ESi064-A), derived from dermal fibroblast from the apparently healthy carrier of the mutation of the gene SACSIN, was generated by non-integrative reprogramming technology using OCT3/4, SOX2, CMYC and KLF4 reprogramming factors. The pluripotency was assessed by immunocytochemist...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2018.10.016
更新日期:2018-12-01 00:00:00
abstract::This study elucidated the stage-specific roles of FGF2 signaling during neural development using in-vitro human embryonic stem cell-based developmental modeling. We found that the dysregulation of FGF2 signaling prior to the onset of neural induction resulted in the malformation of neural rosettes (a neural tube-like ...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2016.08.012
更新日期:2016-09-01 00:00:00
abstract::Recently, many hurdles and limitations for production of clinically applicable iPSC derivatives have been overcome. Transgene-free iPSCs can be efficiently derived from easily accessible cell sources such as blood. Here we describe the generation of transgene-free hiPS cells from cord blood derived CD34+ cells, reprog...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2017.03.022
更新日期:2017-05-01 00:00:00
abstract::An important practical limitation of the three-dimensional geometry of stem-cell derived intestinal organoids is that it prevents easy access to the apical epithelium for testing food components, microorganisms, bioactive and toxic compounds. To this end, we here report on a new robust method for generating confluent ...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2018.02.013
更新日期:2018-04-01 00:00:00
abstract::Reprogramming technology enables the production of neural progenitor cells (NPCs) from somatic cells by direct transdifferentiation. However, little is known on how neural programs in these induced neural stem cells (iNSCs) differ from those of alternative stem cell populations in vitro and in vivo. Here, we performed...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2016.04.015
更新日期:2016-05-01 00:00:00
abstract::Understanding the complex mechanisms that govern the fate decisions of human embryonic stem cells (hESCs) is fundamental to their use in cell replacement therapies. The progress of dissecting these mechanisms will be facilitated by the availability of robust high-throughput screening assays on hESCs. In this study, we...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2010.04.006
更新日期:2010-09-01 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:BACKGROUND:Non-random segregation of DNA strands during stem cell replication has been proposed as a mechanism to minimize accumulated genetic errors in stem cells of rapidly dividing tissues. According to this hypothesis, an "immortal" DNA strand is passed to the stem cell daughter and not the more differentiated cell...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2015.01.005
更新日期:2015-03-01 00:00:00
abstract::The future application of human embryonic stem cells (hESC) for therapeutic approaches requires the development of xeno-free culture conditions to prevent the potential transmission of animal pathogens or xenobiotic substances to hESC. An important component of the majority of hESC culture systems developed is the req...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2010.08.002
更新日期:2011-01-01 00:00:00
abstract::Extracellular signal-regulated kinases (ERKs) have many important functions during embryogenesis. However, their role in embryonic stem (ES) cells is controversial. Previous studies reported that, in contrast to mouse ES cells, human ES cells differentiate if ERK1/2 is inhibited. We reexamined the role of ERK1/2 in hu...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2010.06.002
更新日期:2010-09-01 00:00:00
abstract::We established three iPSC lines from postmortem-cultured fibroblasts derived following the sudden unexpected death of an 8-year-old girl with Lennox-Gastaut syndrome, who turned out to have the R551H-mutant STXBP1 gene. These iPSC clones showed pluripotent characteristics while retaining the genotype and demonstrated ...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101485
更新日期:2019-08-01 00:00:00
abstract::Mesenchymal stem cells (MSC) have been isolated from almost every adult tissue. In cord blood (CB), different non-hematopoietic CD45-, CD34- adherent cell populations can be generated: the cord blood derived MSC (CB-MSC), that behave almost like MSC from bone marrow (BM-MSC), and unrestricted somatic stem cells (USSC)...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2010.03.004
更新日期:2010-07-01 00:00:00
abstract::Induced-pluripotent stem cells (iPSCs) are a potential alternative cell source in regenerative medicine, which includes the use of differentiated iPSCs for cell therapies to treat coronary artery and/or peripheral arterial diseases. Late-outgrowth endothelial progenitor cells (late-EPCs) are a unique primary cell pres...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2012.11.006
更新日期:2013-03-01 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::Asparagine synthetase (ASNS) deficiency (ASNSD; MIM #615574) is a rare neurodevelopmental disorder caused by mutations in the ASNS gene. The ASNS gene maps to cytogenetic band 7q21.3 and is 35 kb long. ASNSD is characterised by congenital microcephaly, severely delayed psychomotor development, seizures, and hyperekple...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101583
更新日期:2019-12-01 00:00:00
abstract::Human embryonic stem cells (hESCs) offer new avenues for studying human development and disease progression in addition to their tremendous potential toward development of cell-replacement therapies for various cellular disorders. We have earlier reported the derivation and characterization of Relicell(®) hES1, the fi...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2010.07.001
更新日期:2010-11-01 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::Parental origin-dependent expression of the imprinted genes is essential for mammalian development. Zfp57 maintains genomic imprinting in mouse embryos and ES cells. To examine the allelic expression patterns of the imprinted genes in ES cells, we obtained multiple hybrid ES clones that were directly derived from the ...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2016.01.017
更新日期:2016-03-01 00:00:00
abstract::Pluripotency is a cellular state of multiple options. Here, we highlight the potential for self-organization to contribute to stem cell fate computation. A new way of considering regulatory circuitry is presented that describes the expression of each transcription factor (TF) as a branching process that propagates thr...
journal_title:Stem cell research
pub_type: 杂志文章,评审
doi:10.1016/j.scr.2011.11.001
更新日期:2012-03-01 00:00:00
abstract::Best's disease (BD) is an inherited retinal degenerative disease caused by mutations in BEST1 gene. A human induced pluripotent stem cell (iPSC) line has been generated with integration-free Sendai virus method from peripheral blood mononuclear cells (PBMCs) of a BD patient carrying c.888C > A mutation in BEST1 gene. ...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101459
更新日期:2019-07-01 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::We sought to elucidate how and when the ocular surface ectoderm commits to its differentiation into the corneal epithelium in eye development from human induced pluripotent stem cells (hiPSCs) under the influence of WNT signaling and the actions of BMP4. These signals are key drivers ocular surface ectodermal cell fat...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.101868
更新日期:2020-07-01 00:00:00
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::Human teratoma is a germ cell tumor that contains normal tissues (e.g., hair, skin or cartilage) differentiated from embryonal germ layers. Because of the feature of this tumor, we hypothesized that human teratomas contain multipotent stem cells that can develop into various non-cancerous normal tissues. In this study...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101633
更新日期:2019-12-01 00:00:00