RESUMO
Reprogramming somatic cells to become induced pluripotent stem cells (iPSCs) by using defined factors represents an important breakthrough in biology and medicine, yet remains inefficient and poorly understood. We therefore devised synthetic factors by fusing the VP16 transactivation domain to OCT4 (also known as Pou5f1), NANOG and SOX2, respectively. These synthetic factors could reprogramme both mouse and human fibroblasts with enhanced efficiency and accelerated kinetics. Remarkably, Oct4-VP16 alone could efficiently reprogramme mouse embryonic fibroblasts (MEFs) into germline-competent iPSCs. Furthermore, episomally delivered synthetic factors could reproducibly generate integration-free iPSCs from MEFs with enhanced efficiency. Our results not only demonstrate the feasibility of engineering more potent reprogramming factors, but also suggest that transcriptional reactivation of OCT4 target genes might be a rate-limiting step in the conversion of somatic cells to pluripotent cells. Synthetic factor-based reprogramming might lead to a paradigm shift in reprogramming research.
Assuntos
Reprogramação Celular/fisiologia , Células-Tronco Pluripotentes Induzidas/citologia , Células-Tronco Pluripotentes Induzidas/metabolismo , Animais , Reprogramação Celular/genética , Proteínas de Homeodomínio/genética , Proteínas de Homeodomínio/metabolismo , Humanos , Camundongos , Fator 3 de Transcrição de Octâmero/genética , Fator 3 de Transcrição de Octâmero/metabolismo , Fatores de Transcrição SOXB1/genética , Fatores de Transcrição SOXB1/metabolismoRESUMO
The mechanism and kinetics for the gas-phase hydrolysis of N(2)O(4) isomers have been investigated at the CCSD(T)/6-311++G(3df,2p)//B3LYP/6-311++G(3df,2p) level of theory in conjunction with statistical rate constant calculations. Calculated results show that the contribution from the commonly assumed redox reaction of sym-N(2)O(4) to the homogeneous gas-phase hydrolysis of NO(2) can be unequivocally ruled out due to the high barrier (37.6 kcal/mol) involved; instead, t-ONONO(2) directly formed by the association of 2NO(2), was found to play the key role in the hydrolysis process. The kinetics for the hydrolysis reaction, 2NO(2) + H(2)O â HONO + HNO(3) (A) can be quatitatively interpreted by the two step mechanism: 2NO(2) â t-ONONO(2), t-ONONO(2) + H(2)O â HONO + HNO(3). The predicted total forward and reverse rate constants for reaction (A), k(tf) = 5.36 × 10(-50)T(3.95) exp(1825/T) cm(6) molecule(-2) s(-1) and k(tr) = 3.31 × 10(-19)T(2.478) exp(-3199/T) cm(3) molecule(-1) s(-1), respectively, in the temperature range 200-2500 K, are in good agreement with the available experimental data.
RESUMO
Lithium-sulfur batteries are among the most promising low-cost, high-energy-density storage devices. However, the inability to host a sufficient amount of sulfur in the cathode while maintaining good electrochemical stability under a lean electrolyte condition has limited the progress. The main cause of these challenges is the sensitivity of the sulfur cathode to the cell-design parameters (i.e., the amount of sulfur and electrolyte) and the experimental testing conditions (i.e., cycling rates and analysis duration). Here, a hot-pressing method is presented that effectively encapsulates a high amount of sulfur in the cathode within only 5 s, resulting in high sulfur loading and content of, respectively, 10 mg cm-2 and 65 wt%. The hot-pressed sulfur (HPS) cathodes exhibit superior dynamic and static electrochemical performance under a broad cycling-rate (C/20-1C rates) and low electrolyte/sulfur ratio (6 µL mg-1 ) conditions. The dynamic cell stability is demonstrated by high gravimetric and areal capacities of, respectively, 415-730 mAh g-1 and 7-12 mAh cm-2 at C/20-1C rates with a high capacity retention of over 70% after 200 cycles. The static cell stability is demonstrated by excellent shelf life with low self-discharge and stable cycle life on storing for over one year.
RESUMO
The ASS1 gene encodes argininosuccinate synthetase-1, a cytosolic enzyme with a critical role in the urea cycle. Mutations are found in all ASS1 exons and cause the autosomal recessive disorder citrullinemia. Using CRISPR/Cas9-editing, we established the WAe001-A-13 cell line, which was heterozygous for an ASS1 mutation, from the human embryonic stem cell line H1. The WAe001-A-13 cell line maintained the pluripotent phenotype, the ability to differentiate into all three germ layers and a normal karyotype.
Assuntos
Argininossuccinato Liase/genética , Sistemas CRISPR-Cas , Células-Tronco Embrionárias Humanas/citologia , Argininossuccinato Liase/antagonistas & inibidores , Argininossuccinato Liase/metabolismo , Sequência de Bases , Linhagem Celular , Heterozigoto , Células-Tronco Embrionárias Humanas/fisiologia , Humanos , Mutação , FenótipoRESUMO
MiR-122 is the most abundant miRNA in the human liver accounting for 52% of the entire hepatic miRNome. Previous studies have demonstrated that miR-122 is a valuable therapeutic target for liver diseases, including viral hepatitis, fibrosis, steatosis, and hepatocarcinoma. Here, we constructed a miR-122 doxycycline-inducible expression human embryonic stem cell line WAe001-A-15 using the piggyBac transposon system. The cell line retained its pluripotency, in vitro differentiation potential, normal morphology, and karyotype.
Assuntos
Doxiciclina/farmacologia , Células-Tronco Embrionárias/citologia , Células-Tronco Embrionárias/metabolismo , MicroRNAs/biossíntese , Células-Tronco Pluripotentes/citologia , Células-Tronco Pluripotentes/metabolismo , Antibacterianos/farmacologia , Linhagem Celular , Elementos de DNA Transponíveis , Células-Tronco Embrionárias/efeitos dos fármacos , Humanos , Células-Tronco Pluripotentes/efeitos dos fármacosRESUMO
Glycogen debranching enzyme (GDE) plays a critical role in glycogenolysis. Mutations in the GDE gene are associated with a metabolic disease known as glycogen storage disease type III (GSDIII). We generated a mutant GDE human embryonic stem cell line, WAe001-A-14, using the CRISPR/Cas9 editing system. This cell line contains a 24-nucleotide deletion within exon-13 of GDE, resulting in 8 amino acids (TRLGISSL) missing of the GDE protein from amino acid position 567 to 575. The WAe001-A-14 cell line maintains typical stem cell morphology, pluripotency and in vitro differentiation potential, and a normal karyotype.
Assuntos
Sistemas CRISPR-Cas/genética , Sistema da Enzima Desramificadora do Glicogênio/genética , Células-Tronco Embrionárias Humanas/metabolismo , Linhagem Celular , Heterozigoto , Humanos , Mutação/genética , Reação em Cadeia da Polimerase em Tempo RealRESUMO
Human pluripotent stem cells (hPSCs) exhibit very limited contribution to interspecies chimeras. One explanation is that the conventional hPSCs are in a primed state and so unable to form chimeras in pre-implantation embryos. Here, we show that the conventional hPSCs undergo rapid apoptosis when injected into mouse pre-implantation embryos. While, forced-expression of BMI1, a polycomb factor in hPSCs overcomes the apoptosis and enables hPSCs to integrate into mouse pre-implantation embryos and subsequently contribute to chimeras with both embryonic and extra-embryonic tissues. In addition, BMI1 also enables hPSCs to integrate into pre-implantation embryos of other species, such as rabbit and pig. Notably, BMI1 high expression and anti-apoptosis are also indicators for naïve hPSCs to form chimera in mouse embryos. Together, our findings reveal that the apoptosis is an initial barrier in interspecies chimerism using hPSCs and provide a rational to improve it.
Assuntos
Quimerismo , Células-Tronco Pluripotentes/metabolismo , Complexo Repressor Polycomb 1/metabolismo , Animais , Apoptose , Blastocisto/citologia , Blastocisto/metabolismo , Linhagem da Célula , Membranas Extraembrionárias/metabolismo , Humanos , Camundongos Endogâmicos ICR , Células-Tronco Pluripotentes/citologia , Coelhos , Especificidade da Espécie , SuínosRESUMO
The MEN1 gene is cytogenetically located at 11q13.1 and encodes the nuclear protein menin, which is involved in cell proliferation, apoptosis, differentiation, and metabolism. Here, we generated two MEN1 knockout human embryonic stem cell lines, WAe001-A-4 and WAe001-A-5, by targeting exon-2 and exon-9 of MEN1 using the CRISPR/Cas9 technique. These cell lines maintained their pluripotency, in vitro differentiation potential, normal morphology, and karyotype. These human MEN1-mutated cell lines not only enlarge the pool of lab resources but also provide ideal models to dissect the detailed physio-pathological roles of the menin protein.
Assuntos
Células-Tronco Embrionárias Humanas/metabolismo , Proteínas Proto-Oncogênicas/genética , Humanos , Proteínas Proto-Oncogênicas/metabolismoRESUMO
The ATP-sensitive potassium channel is an octameric complex, and one of its subunits, namely Kir6.2, is encoded by the KCNJ11 gene. Mutations in KCNJ11 result in hyperinsulinism or diabetes mellitus, associated with abnormal insulin secretion. Here, using CRISPR/Cas9 editing, we established a homozygous mutant KCNJ11 cell line, WAe001-A-12, which was generated by a 62-bp deletion in the coding sequence of the human embryonic stem cell line H1. It was confirmed that this deletion in the KCNJ11 gene did not affect the protein expression levels of key pluripotent factors. Additionally, normal karyotype and differentiation potency were observed for the cell line.
Assuntos
Sistemas CRISPR-Cas/genética , Células-Tronco Embrionárias/metabolismo , Células-Tronco Embrionárias Humanas/metabolismo , Canais de Potássio Corretores do Fluxo de Internalização/genética , Diferenciação Celular , Linhagem Celular , Humanos , Canais de Potássio Corretores do Fluxo de Internalização/metabolismoRESUMO
The gene asialoglycoprotein receptor 1 (ASGR1) encodes a subunit of the asialoglycoprotein receptor. Here we report the generation of a human embryonic stem cell line WAe001-A-6 harbouring homozygous ASGR1 mutations using CRISPR/Cas9. The mutation involves a 37bp deletion, resulting in a frame shift. The homozygous knockout WA01 cell line maintains a normal karyotype, typical stem cell morphology, pluripotency and differentiation potential in vitro.
Assuntos
Receptor de Asialoglicoproteína/genética , Células-Tronco Embrionárias Humanas/citologia , Sequência de Aminoácidos , Receptor de Asialoglicoproteína/metabolismo , Sistemas CRISPR-Cas , Diferenciação Celular/fisiologia , Linhagem Celular , Mutação da Fase de Leitura , Deleção de Genes , Técnicas de Inativação de Genes , Células-Tronco Embrionárias Humanas/metabolismo , Humanos , Fatores de Transcrição/genética , Fatores de Transcrição/metabolismoRESUMO
miR-122 is the most abundant miRNA in the human liver, accounting for 52% of the entire hepatic miRNome. Previous studies have demonstrated that miR-122 plays key roles in hepatocyte growth, metabolism, and homeostasis. Here, we created three miR-122 knockout human embryonic stem cell line lines, WAe001-A-7, WAe001-A-8, and WAe001-A-9, using the CRISPR/Cas9 technique. These mutated cell lines retained their pluripotency, in vitro differentiation potential, normal morphology, and karyotype.
Assuntos
Células-Tronco Embrionárias Humanas/metabolismo , MicroRNAs/genética , Linhagem Celular , Humanos , MicroRNAs/metabolismoRESUMO
Polycomb repressive complex 2 and the epigenetic mark that it deposits, H3K27me3, are evolutionarily conserved and play critical roles in development and cancer. However, their roles in cell fate decisions in early embryonic development remain poorly understood. Here we report that knockout of polycomb repressive complex 2 genes in human embryonic stem cells causes pluripotency loss and spontaneous differentiation toward a meso-endoderm fate, owing to de-repression of BMP signalling. Moreover, human embryonic stem cells with deletion of EZH1 or EZH2 fail to differentiate into ectoderm lineages. We further show that polycomb repressive complex 2-deficient mouse embryonic stem cells also release Bmp4 but retain their pluripotency. However, when converted into a primed state, they undergo spontaneous differentiation similar to that of hESCs. In contrast, polycomb repressive complex 2 is dispensable for pluripotency when human embryonic stem cells are converted into the naive state. Our studies reveal both lineage- and pluripotent state-specific roles of polycomb repressive complex 2 in cell fate decisions.Polycomb repressive complex 2 (PRC2) plays an essential role in development by modifying chromatin but what this means at a cellular level is unclear. Here, the authors show that ablation of PRC2 genes in human embryonic stem cells and in mice results in changes in pluripotency and the primed state of cells.
Assuntos
Diferenciação Celular/genética , Linhagem da Célula/genética , Ectoderma/metabolismo , Células-Tronco Embrionárias Humanas/metabolismo , Células-Tronco Embrionárias Murinas/metabolismo , Complexo Repressor Polycomb 2/genética , Animais , Ectoderma/citologia , Proteína Potenciadora do Homólogo 2 de Zeste/genética , Proteína Potenciadora do Homólogo 2 de Zeste/metabolismo , Técnicas de Inativação de Genes , Células-Tronco Embrionárias Humanas/citologia , Humanos , Camundongos , Camundongos Endogâmicos NOD , Camundongos Knockout , Camundongos SCID , Células-Tronco Embrionárias Murinas/citologia , Complexo Repressor Polycomb 2/metabolismoRESUMO
The gene of ATP-binding cassette subfamily C member 8 (Abcc8) is cytogenetically located at 11p15.1 and encodes the sulfonylurea receptor (SUR1). SUR1 is a subunit of ATP-sensitive potassium channel (KAPT) in the ß-cell regulating insulin secretion. Mutations of ABCC8 are responsible for congenital hyperinsulinism (CHI). Here we generated an Abcc8 homozygous mutant cell line by CRISPR/Cas9 technique with 22bp deletion resulting in abnormal splicing on human embryonic stem cell line H1. The phenotypic characteristics of this cell line reveal defective KATP channel and diazoxide-unresponsive that provides an ideal model for molecular pathology research and drug screening for CHI.
Assuntos
Sistemas CRISPR-Cas/genética , Células-Tronco Embrionárias Humanas/citologia , Hiperinsulinismo/patologia , Receptores de Sulfonilureias/genética , Sequência de Bases , Diferenciação Celular , Linhagem Celular , Corpos Embrioides/citologia , Corpos Embrioides/metabolismo , Homozigoto , Células-Tronco Embrionárias Humanas/metabolismo , Humanos , Hiperinsulinismo/genética , Cariótipo , Masculino , Microscopia de Fluorescência , Alinhamento de Sequência , Fatores de Transcrição/genética , Fatores de Transcrição/metabolismoRESUMO
The gene of ATP-binding cassette subfamily C member 8 (Abcc8) is cytogenetically located at 11p15.1 and encodes the sulfonylurea receptor (SUR1). SUR1 is a subunit of ATP-sensitive potassium channel (KAPT) in the ß-cell regulating insulin secretion. Mutations of ABCC8 are responsible for congenital hyperinsulinism (CHI). Here we reported that an Abcc8 heterozygous mutant cell line was generated by CRISPR/Cas9 technique with 1bp insertion resulting in abnormal splicing on human embryonic stem cell line H1. The phenotypic characteristics of this cell line reveal defective KATP channel and diazoxide-responsive that provides ideal model for molecular pathology research and drug screening for CHI.
Assuntos
Sistemas CRISPR-Cas/genética , Células-Tronco Embrionárias Humanas/citologia , Hiperinsulinismo/patologia , Receptores de Sulfonilureias/genética , Sequência de Bases , Diferenciação Celular , Linhagem Celular , Corpos Embrioides/citologia , Corpos Embrioides/metabolismo , Heterozigoto , Células-Tronco Embrionárias Humanas/metabolismo , Humanos , Hiperinsulinismo/genética , Cariótipo , Masculino , Microscopia de Fluorescência , Mutagênese Insercional , Sítios de Splice de RNA/genética , Alinhamento de Sequência , Fatores de Transcrição/genética , Fatores de Transcrição/metabolismoRESUMO
Recent studies have boosted our understanding of long noncoding RNAs (lncRNAs) in numerous biological processes, but few have examined their roles in somatic cell reprogramming. Through expression profiling and functional screening, we have identified that the large intergenic noncoding RNA p21 (lincRNA-p21) impairs reprogramming. Notably, lincRNA-p21 is induced by p53 but does not promote apoptosis or cell senescence in reprogramming. Instead, lincRNA-p21 associates with the H3K9 methyltransferase SETDB1 and the maintenance DNA methyltransferase DNMT1, which is facilitated by the RNA-binding protein HNRNPK. Consequently, lincRNA-p21 prevents reprogramming by sustaining H3K9me3 and/or CpG methylation at pluripotency gene promoters. Our results provide insight into the role of lncRNAs in reprogramming and establish a novel link between p53 and heterochromatin regulation.
Assuntos
Reprogramação Celular , Ilhas de CpG , Metilação de DNA , Células-Tronco Pluripotentes Induzidas/metabolismo , RNA Longo não Codificante/metabolismo , Proteína Supressora de Tumor p53/metabolismo , Animais , Apoptose , Proliferação de Células , DNA (Citosina-5-)-Metiltransferase 1 , DNA (Citosina-5-)-Metiltransferases/metabolismo , Heterocromatina/genética , Heterocromatina/metabolismo , Histona-Lisina N-Metiltransferase/metabolismo , Histonas/genética , Histonas/metabolismo , Células-Tronco Pluripotentes Induzidas/citologia , Camundongos , Regiões Promotoras GenéticasRESUMO
Vitamin C, a micronutrient known for its anti-scurvy activity in humans, promotes the generation of induced pluripotent stem cells (iPSCs) through the activity of histone demethylating dioxygenases. TET hydroxylases are also dioxygenases implicated in active DNA demethylation. Here we report that TET1 either positively or negatively regulates somatic cell reprogramming depending on the absence or presence of vitamin C. TET1 deficiency enhances reprogramming, and its overexpression impairs reprogramming in the context of vitamin C by modulating the obligatory mesenchymal-to-epithelial transition (MET). In the absence of vitamin C, TET1 promotes somatic cell reprogramming independent of MET. Consistently, TET1 regulates 5-hydroxymethylcytosine (5hmC) formation at loci critical for MET in a vitamin C-dependent fashion. Our findings suggest that vitamin C has a vital role in determining the biological outcome of TET1 function at the cellular level. Given its benefit to human health, vitamin C should be investigated further for its role in epigenetic regulation.