RESUMEN
Whereas oncogenes can potentially be inhibited with small molecules, the loss of tumour suppressors is more common and is problematic because the tumour-suppressor proteins are no longer present to be targeted. Notable examples include SMARCB1-mutant cancers, which are highly lethal malignancies driven by the inactivation of a subunit of SWI/SNF (also known as BAF) chromatin-remodelling complexes. Here, to generate mechanistic insights into the consequences of SMARCB1 mutation and to identify vulnerabilities, we contributed 14 SMARCB1-mutant cell lines to a near genome-wide CRISPR screen as part of the Cancer Dependency Map Project1-3. We report that the little-studied gene DDB1-CUL4-associated factor 5 (DCAF5) is required for the survival of SMARCB1-mutant cancers. We show that DCAF5 has a quality-control function for SWI/SNF complexes and promotes the degradation of incompletely assembled SWI/SNF complexes in the absence of SMARCB1. After depletion of DCAF5, SMARCB1-deficient SWI/SNF complexes reaccumulate, bind to target loci and restore SWI/SNF-mediated gene expression to levels that are sufficient to reverse the cancer state, including in vivo. Consequently, cancer results not from the loss of SMARCB1 function per se, but rather from DCAF5-mediated degradation of SWI/SNF complexes. These data indicate that therapeutic targeting of ubiquitin-mediated quality-control factors may effectively reverse the malignant state of some cancers driven by disruption of tumour suppressor complexes.
Asunto(s)
Complejos Multiproteicos , Mutación , Neoplasias , Proteína SMARCB1 , Animales , Femenino , Humanos , Masculino , Ratones , Línea Celular Tumoral , Sistemas CRISPR-Cas , Edición Génica , Neoplasias/genética , Neoplasias/metabolismo , Proteína SMARCB1/deficiencia , Proteína SMARCB1/genética , Proteína SMARCB1/metabolismo , Proteínas Supresoras de Tumor/deficiencia , Proteínas Supresoras de Tumor/genética , Proteínas Supresoras de Tumor/metabolismo , Complejos Multiproteicos/química , Complejos Multiproteicos/metabolismo , Proteolisis , Ubiquitina/metabolismoRESUMEN
For cells to initiate and sustain a differentiated state, it is necessary that a 'memory' of this state is transmitted through mitosis to the daughter cells1-3. Mammalian switch/sucrose non-fermentable (SWI/SNF) complexes (also known as Brg1/Brg-associated factors, or BAF) control cell identity by modulating chromatin architecture to regulate gene expression4-7, but whether they participate in cell fate memory is unclear. Here we provide evidence that subunits of SWI/SNF act as mitotic bookmarks to safeguard cell identity during cell division. The SWI/SNF core subunits SMARCE1 and SMARCB1 are displaced from enhancers but are bound to promoters during mitosis, and we show that this binding is required for appropriate reactivation of bound genes after mitotic exit. Ablation of SMARCE1 during a single mitosis in mouse embryonic stem cells is sufficient to disrupt gene expression, impair the occupancy of several established bookmarks at a subset of their targets and cause aberrant neural differentiation. Thus, SWI/SNF subunit SMARCE1 has a mitotic bookmarking role and is essential for heritable epigenetic fidelity during transcriptional reprogramming.
Asunto(s)
Diferenciación Celular , Proteínas Cromosómicas no Histona , Epigénesis Genética , Mitosis , Animales , Ratones , Diferenciación Celular/genética , Cromatina/genética , Ensamble y Desensamble de Cromatina/genética , Proteínas Nucleares/metabolismo , Factores de Transcripción/metabolismo , Mitosis/genética , Proteínas Cromosómicas no Histona/deficiencia , Proteínas Cromosómicas no Histona/genética , Proteínas Cromosómicas no Histona/metabolismo , Subunidades de Proteína/metabolismo , Células Madre Embrionarias de Ratones/metabolismo , Elementos de Facilitación Genéticos/genética , Regiones Promotoras Genéticas/genética , División Celular/genética , Epigénesis Genética/genéticaRESUMEN
The identification of mechanisms to promote memory T (Tmem) cells has important implications for vaccination and anti-cancer immunotherapy1-4. Using a CRISPR-based screen for negative regulators of Tmem cell generation in vivo5, here we identify multiple components of the mammalian canonical BRG1/BRM-associated factor (cBAF)6,7. Several components of the cBAF complex are essential for the differentiation of activated CD8+ T cells into T effector (Teff) cells, and their loss promotes Tmem cell formation in vivo. During the first division of activated CD8+ T cells, cBAF and MYC8 frequently co-assort asymmetrically to the two daughter cells. Daughter cells with high MYC and high cBAF display a cell fate trajectory towards Teff cells, whereas those with low MYC and low cBAF preferentially differentiate towards Tmem cells. The cBAF complex and MYC physically interact to establish the chromatin landscape in activated CD8+ T cells. Treatment of naive CD8+ T cells with a putative cBAF inhibitor during the first 48 h of activation, before the generation of chimeric antigen receptor T (CAR-T) cells, markedly improves efficacy in a mouse solid tumour model. Our results establish cBAF as a negative determinant of Tmem cell fate and suggest that manipulation of cBAF early in T cell differentiation can improve cancer immunotherapy.
Asunto(s)
Linfocitos T CD8-positivos , Diferenciación Celular , ADN Helicasas , Complejos Multiproteicos , Proteínas Nucleares , Proteínas Proto-Oncogénicas c-myc , Factores de Transcripción , Animales , Linfocitos T CD8-positivos/citología , ADN Helicasas/metabolismo , Modelos Animales de Enfermedad , Memoria Inmunológica , Inmunoterapia , Células T de Memoria/citología , Ratones , Complejos Multiproteicos/química , Complejos Multiproteicos/metabolismo , Neoplasias , Proteínas Nucleares/metabolismo , Proteínas Proto-Oncogénicas c-myc/metabolismo , Receptores Quiméricos de Antígenos , Factores de Transcripción/metabolismoRESUMEN
Mouse embryonic stem cells derived from the epiblast contribute to the somatic lineages and the germline but are excluded from the extra-embryonic tissues that are derived from the trophectoderm and the primitive endoderm upon reintroduction to the blastocyst. Here we report that cultures of expanded potential stem cells can be established from individual eight-cell blastomeres, and by direct conversion of mouse embryonic stem cells and induced pluripotent stem cells. Remarkably, a single expanded potential stem cell can contribute both to the embryo proper and to the trophectoderm lineages in a chimaera assay. Bona fide trophoblast stem cell lines and extra-embryonic endoderm stem cells can be directly derived from expanded potential stem cells in vitro. Molecular analyses of the epigenome and single-cell transcriptome reveal enrichment for blastomere-specific signature and a dynamic DNA methylome in expanded potential stem cells. The generation of mouse expanded potential stem cells highlights the feasibility of establishing expanded potential stem cells for other mammalian species.
Asunto(s)
Blastómeros/citología , Células Madre Embrionarias de Ratones/citología , Animales , Blastocisto/citología , Blastómeros/metabolismo , Linaje de la Célula , Células Cultivadas , Quimera , Embrión de Mamíferos/citología , Endodermo/citología , Epigénesis Genética , Epigenómica , Femenino , Masculino , Ratones , Células Madre Embrionarias de Ratones/metabolismo , Placenta/citología , Células Madre Pluripotentes/citología , Células Madre Pluripotentes/metabolismo , Embarazo , Análisis de la Célula Individual , Transcriptoma , Trofoblastos/citologíaRESUMEN
Signaling pathways transmit extracellular cues into cells and regulate transcriptome and epigenome to maintain or change the cell identity. Protein kinases and phosphatases are critical for signaling transduction and regulation. Here, we report that CDK11, a member of the CDK family, is required for the maintenance of human embryonic stem cell (hESC) self-renewal. Our results show that, among the three main isoforms of CDK11, CDK11p46 is the main isoform safeguarding the hESC identity. Mechanistically, CDK11 constrains two important mitogen-activated protein kinase (MAPK) signaling pathways (JNK and p38 signaling) through modulating the activity of protein phosphatase 1. Furthermore, CDK11 knockdown activates transforming growth factor ß (TGF-ß)/SMAD2/3 signaling and upregulates certain nonneural differentiation-associated genes. Taken together, this study uncovers a kinase required for hESC self-renewal through fine-tuning MAPK and TGF-ß signaling at appropriate levels. The kinase-phosphatase axis reported here may shed new light on the molecular mechanism sustaining the identity of hESCs.
Asunto(s)
Quinasas Ciclina-Dependientes/metabolismo , Células Madre Embrionarias/fisiología , Transducción de Señal/fisiología , Proliferación Celular , Quinasas Ciclina-Dependientes/genética , Regulación hacia Abajo , Regulación de la Expresión Génica , Técnicas de Silenciamiento del Gen , Humanos , MAP Quinasa Quinasa 4/genética , MAP Quinasa Quinasa 4/metabolismo , Quinasas de Proteína Quinasa Activadas por Mitógenos/genética , Quinasas de Proteína Quinasa Activadas por Mitógenos/metabolismo , Isoformas de Proteínas , Proteína Smad2/genética , Proteína Smad2/metabolismo , Proteína smad3/genética , Proteína smad3/metabolismo , Factor de Crecimiento Transformador beta/genética , Factor de Crecimiento Transformador beta/metabolismo , Regulación hacia Arriba , Proteínas Quinasas p38 Activadas por Mitógenos/genética , Proteínas Quinasas p38 Activadas por Mitógenos/metabolismoRESUMEN
In this study, the porous graphite phase carbon nitride photocatalyst (P-g-C3N4) is prepared by the CaCO3 template method, and then P-g-C3N4/T-polyethylene terephthalate (T-PET) catalytic fibre is prepared by the padding method. P-g-C3N4 can provide more active sites than g-C3N4 as proved by the Brunauer-Emmett-Teller and the UV-Visible diffuse reflectance test. P-g-C3N4 powder catalyst successfully supports PET fibre as proved by scanning electron microscope, Fourier infrared spectroscopy and X-ray diffraction spectroscopy. The photocatalytic performance of P-g-C3N4/T-PET catalytic fibre is tested by constructing a single hexavalent chromium or hexavalent chromium/organic pollutant binary pollution system. The potential application value of P-g-C3N4/T-PET catalytic fibre is further explored by simulating the complex actual water environment. After five recycles, P-g-C3N4/T-PET catalytic fibre shows good catalytic performance. The mechanism of P-g-C3N4/PET photocatalytic degradation of organic pollutants is proposed through the capture agent experiment and electron paramagnetic resonance spectroscopy. Among them, â¢O2- is the most important active species of P-g-C3N4 catalytic fibre, which is used for the oxidation of organic pollutants. At the same time, photoelectrons generated by the catalytic fibre are used to reduce hexavalent chromium. The efficiency of P-g-C3N4 to remove pollutants is improved by using PET fibre as a carrier, which not only solves the problem of difficult recovery of powder catalysts but also provides more active sites.
RESUMEN
Iron (II) phthalocyanine (FePc) is loaded on the surface of the tourmaline (TM) by the reflow method to obtain FePc/TM. This research effectively prevents the π-π stacking of FePc, increased the effective utilization rate of PMS activation under solar light, and further improved the catalytic performance of the catalytic system. The catalytic oxidation efficiency of FePc/TM on carbamazepine (CBZ) and sulfadiazine (SD) can reach 99% under solar light for 15 and 5â min, the total organic carbon (TOC) removal rate can reach 58% and 69% under solar light for 120â min. After 6 cycles, the CBZ removal rate remained above 95%. In addition, the FePc/TM catalytic system has an excellent removal rate for other pharmaceuticals. The results of spin-trapped electron paramagnetic resonance and classical quenching experiments show that FePc/TM can effectively activate PMS to generate active species under solar light, including superoxide radical (â¢O2-), singlet oxygen (1O2), hydroxyl radicals(â¢OH), and sulphate radicals (SO4â¢-). The intermediates of CBZ were identified by Ultra-high performance liquid chromatography and high resolution mass spectrometry, and the degradation pathway was proposed. As the reaction progresses, all CBZ and intermediates are reduced and converted into small acids, or mineralized to H2O, CO2. This work provides an alternative method for the design of efficient activation of PMS activation catalysts under solar light to eliminate residual pharmaceuticals in actual water bodies.
Asunto(s)
Hierro , Peróxidos , Hierro/química , Peróxidos/química , Preparaciones FarmacéuticasRESUMEN
In this study, each cobalt tetra-aminophthalocyanine (CoTAPc) molecule was immobilised with four isonicotinic acid (INA) molecules by amide bonding, a novel and highly efficient catalyst pyridine-bridged cobalt tetra-aminophthalocyanine (CoTAPc-TINA) was synthesised. The introduction of INA molecules promoted CoTAPc to expose more active sites, and increased the electron cloud density of cobalt ions promoting O-O bond homolysis of PMS to generate more active species, which significantly enhanced catalytic activity. With the pharmaceutical of carbamazepine (CBZ) as model pollutant, 0.1 g/L CoTAPc-TINA in dark in the presence of 0.4 mM PMS, 98.8% CBZ was removed within 10 min. However, under the same conditions the removed of CBZ was only 58.9% by CoTAPc/PMS system. Radical capture experiments combined electron paramagnetic resonance technology demonstrate that hydroxyl radicals, sulphate radicals, superoxide radicals and singlet oxygen are the main active species in the CoTAPc-TINA/PMS system. As the reaction proceeded, all aromatic intermediates were transformed to small molecular acids by these active species. This investigation provided a new insight for application of metal phthalocyanine in wastewater treatment.
RESUMEN
The current environmental problems urgently require researchers to seek an environmentally friendly, effective and easy to operate sewage treatment method. Graphite carbon nitride (g-C3N4), which has the advantages of simple preparation, safety, non-toxicity and chemical resistance, was expected to become a photocatalyst for solving environmental pollution. However, the performances of g-C3N4 still have some limitations that the electron hole recombination is fast and the powder is not easy to recover. In this study, zinc-doped graphite carbon nitride photocatalyst (Zn-g-C3N4) was mixed with polyacrylonitrile (PAN) to produce photocatalyst fibres by electrospinning. It not only solves the problem that the powder catalyst is difficult to recycle, but also effectively inhibits the recombination of photoelectron-hole pairs. Zn-g-C3N4/PAN has good photocatalytic activity for the simultaneous reduction of hexavalent chromium and degradation of pharmaceuticals. When organic pollutants are present, the reduction efficiency of hexavalent chromium was improved without affecting its own removal efficiency. The potential application value of Zn-g-C3N4/PAN catalytic fibre was further explored by simulating the complex actual water environment. The composite fibre can be easily reused and keep its superior photocatalytic performance. The mechanism of pharmaceuticals degradation was proposed, in which âO2- is the most important active species, which leads to the oxidation of pharmaceuticals. Besides, the photoelectrons generated by the catalyst can reduce the toxic hexavalent chromium. The efficiency of Zn-g-C3N4 to remove pollutants is improved by PAN fibre as a carrier, which not only solves the problem of difficult recovery of powder catalysts, but also provides more active sites.
Asunto(s)
Contaminantes Ambientales , Grafito , Catálisis , Cromo , Grafito/química , Compuestos de Nitrógeno , Compuestos Orgánicos , Polvos , ZincRESUMEN
The local coordination structure of metal atoms in single-atom catalysts (SACs) greatly influences their catalytic performance. And for most SACs, single metal atoms were anchored on carbon materials with N or C coordination. However, the rational design of oxygen-containing SACs and analyzing its structure-performance relationship remain challenging. Herein, we used amino-rich compounds to tailor the metatungstate and fix the W atoms and finally obtained the oxygen-containing W-SACs. The structural evolution of tungsten and its coordination atoms were tracked by electrospray ionization high-definition mass spectrometry. Furthermore, aberration-corrected transmission electron microscopy, X-ray absorption fine-structure spectroscopy, and first-principles calculation results revealed that different from the traditional SACs, the WO2N2 moiety (W coordinated with two O atoms and two N atoms) may be the favored structure for W species. This special structure promoted the energy transfer for enhancing singlet oxygen generation. This work presents an efficient way to prepare more high-efficiency SACs by atomic-scale tailoring and structural evolution tracking at the molecular level.
RESUMEN
The overuse of antimicrobials has resulted in serious damage to the ecosystem and human health. Therefore, the development of an efficient, stable, and reusable catalyst to eliminate antimicrobials under mild conditions is highly desired. Drawing inspiration from the metabolism of drugs by the enzymes in the human body, such as heme catalase, we developed a simulated enzyme catalyst, perchloride iron phthalocyanine (FePcCl16), immobilized on pyridine-modified multiwalled carbon nanotubes (FePcCl16-Py-MWCNTs). In the catalyst, FePcCl16 worked as the active site, and the axial fifth ligand, 4-aminopyridine, was introduced to cleave H2O2 heterolytically. Inspired by the reaction mechanism of heme catalase and H2O2, the catalytic system was designed based on FePcCl16-Py-MWCNTs for oxidizing 4-chloro-3,5-dimethylphenol (PCMX) by H2O2 activation. The results showed that the catalytic activity of the system was significantly increased under simulated solar light irradiation, which can promote electron transfer for heterolytic cleavage of H2O2. The enzyme-like catalyst achieved much higher catalytic activity than the Fenton reaction when the pH was close to neutral. It turned out that the main active species was high-valent iron-oxo (Fe(â £) = O) rather than hydroxyl radial (â¢OH) or superoxide radical (â¢O2-), different from most mechanisms. Ultraperformance liquid chromatography-high-definition mass spectrometry showed that the substrate was degraded to small molecule acids by Fe(â £) = O active species and further mineralization indicated by total organic carbon. The catalytic system exhibited highly efficient, stable, recyclable catalytic performance under mild conditions and did not cause secondary pollution to the environment. This study of a simulated enzyme catalytic system offers important insight into sewage treatment.
Asunto(s)
Antiinfecciosos , Nanotubos de Carbono , Catálisis , Ecosistema , Humanos , Peróxido de Hidrógeno , Hierro , Oxidación-Reducción , PiridinasRESUMEN
BAF complexes are composed of different subunits with varying functional and developmental roles, although many subunits have not been examined in depth. Here we show that the Baf45 subunit Dpf2 maintains pluripotency and ESC differentiation potential. Dpf2 co-occupies enhancers with Oct4, Sox2, p300, and the BAF subunit Brg1, and deleting Dpf2 perturbs ESC self-renewal, induces repression of Tbx3, and impairs mesendodermal differentiation without dramatically altering Brg1 localization. Mesendodermal differentiation can be rescued by restoring Tbx3 expression, whose distal enhancer is positively regulated by Dpf2-dependent H3K27ac maintenance and recruitment of pluripotency TFs and Brg1. In contrast, the PRC2 subunit Eed binds an intragenic Tbx3 enhancer to oppose Dpf2-dependent Tbx3 expression and mesendodermal differentiation. The PRC2 subunit Ezh2 likewise opposes Dpf2-dependent differentiation through a distinct mechanism involving Nanog repression. Together, these findings delineate distinct mechanistic roles for specific BAF and PRC2 subunits during ESC differentiation.
Asunto(s)
Diferenciación Celular , Proteínas de Unión al ADN/fisiología , Células Madre Embrionarias/citología , Complejo Represivo Polycomb 2/metabolismo , Proteínas de Dominio T Box/metabolismo , Factores de Transcripción/fisiología , Animales , Apoptosis , Ciclo Celular , Células Madre Embrionarias/metabolismo , Histonas/genética , Histonas/metabolismo , Ratones , Ratones Noqueados , Proteína Homeótica Nanog/genética , Proteína Homeótica Nanog/metabolismo , Complejo Represivo Polycomb 2/genética , Subunidades de Proteína , Proteínas de Dominio T Box/genéticaRESUMEN
Loss-of-function studies are critically important in gene functional analysis of model organisms and cells. However, conditional gene inactivation in diploid cells is difficult to achieve, as it involves laborious vector construction, multifold electroporation, and complicated genotyping. Here, a strategy is presented for generating biallelic conditional gene and DNA regulatory region knockouts in mouse embryonic stem cells by codelivery of CRISPR-Cas9 and short-homology-arm targeting vectors sequentially or simultaneously. Collectively, a simple and rapid method was presented to knock out any DNA element conditionally. This approach will facilitate the functional studies of essential genes and regulatory regions during development.
RESUMEN
The chromatin landscape and cellular metabolism both contribute to cell fate determination, but their interplay remains poorly understood. Using genome-wide siRNA screening, we have identified prohibitin (PHB) as an essential factor in self-renewal of human embryonic stem cells (hESCs). Mechanistically, PHB forms protein complexes with HIRA, a histone H3.3 chaperone, and stabilizes the protein levels of HIRA complex components. Like PHB, HIRA is required for hESC self-renewal. PHB and HIRA act together to control global deposition of histone H3.3 and gene expression in hESCs. Of particular note, PHB and HIRA regulate the chromatin architecture at the promoters of isocitrate dehydrogenase genes to promote transcription and, thus, production of α-ketoglutarate, a key metabolite in the regulation of ESC fate. Our study shows that PHB has an unexpected nuclear role in hESCs that is required for self-renewal and that it acts with HIRA in chromatin organization to link epigenetic organization to a metabolic circuit.
Asunto(s)
Proteínas de Ciclo Celular/metabolismo , Epigénesis Genética , Chaperonas de Histonas/metabolismo , Células Madre Embrionarias Humanas/metabolismo , Proteínas Represoras/metabolismo , Factores de Transcripción/metabolismo , Autorrenovación de las Células/genética , Cromatina/metabolismo , Inmunoprecipitación de Cromatina , Genes del Desarrollo , Genoma Humano , Células HEK293 , Histonas/metabolismo , Células Madre Embrionarias Humanas/citología , Humanos , Isocitrato Deshidrogenasa/metabolismo , Ácidos Cetoglutáricos/metabolismo , Masculino , Células Madre Pluripotentes/citología , Células Madre Pluripotentes/metabolismo , Prohibitinas , Regiones Promotoras Genéticas , Unión Proteica/genética , ARN Interferente Pequeño/metabolismoRESUMEN
Iron (II) phthalocyanine (FePc) molecules were isolated in polyacrylonitrile (PAN) nanofibers by electrospinning to prevent the formation of dimers and oligomers. Carbamazepine (CBZ) and Rhodamine B (RhB) degradation was investigated during a Fenton-like process with FePc/PAN nanofibers. Classical quenching tests with isopropanol and electron paramagnetic resonance tests with 5,5-dimethyl-pyrroline-oxide as spin-trapping agent were performed to determine the formation of active species during hydrogen peroxide (H2O2) decomposition by FePc/PAN nanofibers. After eight recycles for CBZ degradation over the FePc/PAN nanofibers/H2O2 system, the removal ratios of CBZ remained at 99%. Seven by-products of RhB and twelve intermediates of CBZ were identified using ultra-performance liquid chromatography and high-resolution mass spectrometry. Pathways of CBZ and RhB degradation were proposed based on the identified intermediates. As the reaction proceeded, all CBZ and RhB aromatic nucleus intermediates decreased and were transformed to small acids, but also to potentially toxic epoxide-containing intermediates and acridine, because of the powerful oxidation ability of â¢OH in the catalytic system.
Asunto(s)
Resinas Acrílicas/química , Peróxido de Hidrógeno/química , Indoles/química , Hierro/química , Nanofibras/química , Contaminantes Químicos del Agua/química , Carbamazepina/química , Carbamazepina/aislamiento & purificación , Catálisis , Cromatografía Líquida de Alta Presión , Isoindoles , Espectrometría de Masas/métodos , Modelos Químicos , Estructura Molecular , Oxidación-Reducción , Rodaminas/química , Espectroscopía Infrarroja por Transformada de Fourier , Eliminación de Residuos Líquidos/métodos , Aguas Residuales/química , Contaminantes Químicos del Agua/aislamiento & purificación , Difracción de Rayos XRESUMEN
For powder catalysts to be recycled easily and to be applied in practical wastewater treatment, it is imperative to search suitable carriers that can be applied to support catalytic particles. Herein, we highlight a facile route to synthesize an easily recycled photocatalyst using polyethylene terephthalate (PET) to disperse graphitic carbon nitride (g-C3N4) via electrospinning and subsequent hydrothermal treatment. The resultant nanofiber is labeled T-g-C3N4/PET. The design concept is to expose the g-C3N4 on the PET surface and convert it from inactivation to re-emergence. g-C3N4 is embedded into the PET, which avoids the reunion and unrecyclable deficiencies of powder catalysts. T-g-C3N4/PET was characterized by field-emission scanning electronic microscopy, transmission electron microscopy, UV-vis diffuse reflectance spectra, two-dimensional X-ray diffraction, Fourier-transform infrared spectroscopy, and thermogravimetric analysis technologies. T-g-C3N4/PET showed a high photocatalytic activity for the degradation of antibiotics such as sulfaquinoxaline and sulfadiazine under solar irradiation, and the activity was almost unaffected in a high background. The as-obtained catalysts could be reused several times with no loss in performance in cycling photodegradation tests. Finally, a possible pathway and mechanism for degrading sulfaquinoxaline with T-g-C3N4/PET was proposed, respectively, in which holes and the superoxide radical were the predominant active species, and resulted in the oxidative degradation of antibiotics. These results demonstrate that the preparation method may provide a novel idea for supporting nanoscale catalysts for reuse.
RESUMEN
The effective elimination of micropollutants by an environmentally friendly method has received extensive attention recently. In this study, a photocatalyst based on polyacrylonitrile (PAN)-supported graphitic carbon nitride coupled with zinc phthalocyanine nanofibers (g-C3N4/ZnTcPc/PAN nanofibers) was successfully prepared, where g-C3N4/ZnTcPc was introduced as the catalytic entity and the PAN nanofibers were employed as support to overcome the defects of easy aggregation and difficult recycling. Herein, rhodamine B (RhB), 4-chlorophenol and carbamazepine (CBZ) were selected as the model pollutants. Compared with the typical hydroxyl radical-dominated catalytic system, g-C3N4/ZnTcPc/PAN nanofibers displayed the targeted adsorption and degradation of contaminants under visible light or solar irradiation in the presence of high additive concentrations. According to the results of the radical scavenging techniques and the electron paramagnetic resonance technology, the degradation of target substrates was achieved by the attack of active species, including photogenerated hole, singlet oxygen, superoxide radicals and hydroxyl radicals. Based on the results of ultra-performance liquid chromatography and mass spectrometry, the role of free radicals on the photocatalytic degradation intermediates was identified and the final photocatalytic degradation products of both RhB and CBZ were some biodegradable small molecules.
RESUMEN
Mesenchymal stem cells (MSCs) have great potential for treating various diseases, especially those related to tissue damage involving immune reactions. Various studies have demonstrated that MSCs are strongly immunosuppressive in vitro and in vivo. Our recent studies have shown that un-stimulated MSCs are indeed incapable of immunosuppression; they become potently immunosuppressive upon stimulation with the supernatant of activated lymphocytes, or with combinations of IFN-gamma with TNF-alpha, IL-1alpha or IL-1beta. This observation revealed that under certain circumstances, inflammatory cytokines can actually become immunosuppressive. We showed that there is a species variation in the mechanisms of MSC-mediated immunosuppression: immunosuppression by cytokine-primed mouse MSCs is mediated by nitric oxide (NO), whereas immunosuppression by cytokine-primed human MSCs is executed through indoleamine 2, 3-dioxygenase (IDO). Additionally, upon stimulation with the inflammatory cytokines, both mouse and human MSCs secrete several leukocyte chemokines that apparently serve to attract immune cells into the proximity with MSCs, where NO or IDO is predicted to be most active. Therefore, immunosuppression by inflammatory cytokine-stimulated MSCs occurs via the concerted action of chemokines and immune-inhibitory NO or IDO produced by MSCs. Thus, our results provide novel information about the mechanisms of MSC-mediated immunosuppression and for better application of MSCs in treating tissue injuries induced by immune responses.