Search

BACKGROUND AND AIMS: The scarcity of suitable donor livers highlights a continuing need for innovation to recover organs with reversible injuries in liver transplantation. APPROACH AND RESULTS: Explanted human donor livers (n = 5) declined for transplantation were supported using xenogeneic cross-circulation of whole blood between livers and xeno-support swine. Livers and swine were assessed over 24 hours of xeno-support. Livers maintained normal global appearance, uniform perfusion, and preservation of histologic and subcellular architecture. Oxygen consumption increased by 75% ( p = 0.16). Lactate clearance increased from -0.4 ± 15.5% to 31.4 ± 19.0% ( p = 0.02). Blinded histopathologic assessment demonstrated improved injury scores at 24 hours compared with 12 hours. Vascular integrity and vasoconstrictive function were preserved. Bile volume and cholangiocellular viability markers improved for all livers. Biliary structural integrity was maintained. CONCLUSIONS: Xenogeneic cross-circulation provided multisystem physiological regulation of ex vivo human livers that enabled functional rehabilitation, histopathologic recovery, and improvement of viability markers. We envision xenogeneic cross-circulation as a complementary technique to other organ-preservation technologies in the recovery of marginal donor livers or as a research tool in the development of advanced bioengineering and pharmacologic strategies for organ recovery and rehabilitation.

The prolonged COVID-19 pandemic has disrupted the TVET professional development training, which was planned to be carried out in a face-to-face manner. This study aims to examine TVET professional development training based on the ADDIE model and provide implications for ODA and TVET professional development training in the post-COVID era. In this case study, a TVET training program for Botswana was developed based on the ADDIE model in an untact environment. Accordingly, the performance activities for each phase of analysis, design, development, implementation, and evaluation were analyzed, and based on this, implications for ODA and TVET were provided. This study identified the applicability of non-face-to-face education in the ODA project. Also, this study explored how to develop systematic and dimensional programs based on the ADDIE model in a non-face-to-face manner. In addition, sustainability could be secured through cooperative partnerships between donor and beneficiary countries from the perspective of SDGs Goal.

This data publication contains the compilation of global heat-flow data by the International Heat Flow Commission (IHFC; http://www.ihfc-iugg.org/) of the International Association of Seismology and Physics of the Earth's Interior (IASPEI). The presented data release 2021 contains data generated between 1939 and 2021 and constitutes an updated and extended version of the 2012 IHFC database release (IHFC 2012; later re-published as PANGAEA release: Global Heat Flow Compilation Group, 2013). The 2021 release contains 74,548 heat-flow data from 1,403 publications. 55% of the reported heat-flow values are from the continental domain (n ~ 40,870), while the remaining 45% are located in the oceanic domain (n ~ 33,678). The data are provided in csv and Excel formats. Compared to earlier compilations, which followed the structure defined by Jessop et al. (1976), the new data release was transformed to the recently redefined structure for reporting and storing heat-flow data in the Global Heat Flow Database (Fuchs et al., 2021). Therefore, the notation and structure of the database was adopted, transforming the database field entries defined after Jessop et al. (1976) to the new field structure. Old code notations are not continued and the dataset was cleaned for entries without reporting any heat-flow value. Although successfully transformed, this release marks an intermediate step as the majority of the newly defined database fields have not been filled yet. Filling these fields, checking the existing entries and assessing the quality of each entry are the aim of the upcoming Global Heat Flow Data Assessment Project, for which this data set provides the basis. Consequently, we kindly ask the user to take notice that the current release still suffers similar problems as previously published compilations in terms of data heterogeneity, documentation and quality.

Extracellular vesicles and exomere nanoparticles are under intense investigation as sources of clinically relevant cargo. Here we report the discovery of a distinct extracellular nanoparticle, termed supermere. Supermeres are morphologically distinct from exomeres and display a markedly greater uptake in vivo compared with small extracellular vesicles and exomeres. The protein and RNA composition of supermeres differs from small extracellular vesicles and exomeres. Supermeres are highly enriched with cargo involved in multiple cancers (glycolytic enzymes, TGFBI, miR-1246, MET, GPC1 and AGO2), Alzheimer's disease (APP) and cardiovascular disease (ACE2, ACE and PCSK9). The majority of extracellular RNA is associated with supermeres rather than small extracellular vesicles and exomeres. Cancer-derived supermeres increase lactate secretion, transfer cetuximab resistance and decrease hepatic lipids and glycogen in vivo. This study identifies a distinct functional nanoparticle replete with potential circulating biomarkers and therapeutic targets for a host of human diseases.

This data publication contains the compilation of global heat-flow data by the International Heat Flow Commission (IHFC; http://www.ihfc-iugg.org/) of the International Association of Seismology and Physics of the Earth's Interior (IASPEI). The presented data release 2021 contains data generated between 1939 and 2021 and constitutes an updated and extended version of the 2012 IHFC database release (IHFC 2012; later re-published as PANGAEA release: Global Heat Flow Compilation Group, 2013). The 2021 release contains 74,548 heat-flow data from 1,403 publications. 55% of the reported heat-flow values are from the continental domain (n ~ 40,870), while the remaining 45% are located in the oceanic domain (n ~ 33,678). The data are provided in csv and Excel formats. Compared to earlier compilations, which followed the structure defined by Jessop et al. (1976), the new data release was transformed to the recently redefined structure for reporting and storing heat-flow data in the Global Heat Flow Database (Fuchs et al., 2021). Therefore, the notation and structure of the database was adopted, transforming the database field entries defined after Jessop et al. (1976) to the new field structure. Old code notations are not continued and the dataset was cleaned for entries without reporting any heat-flow value. Although successfully transformed, this release marks an intermediate step as the majority of the newly defined database fields have not been filled yet. Filling these fields, checking the existing entries and assessing the quality of each entry are the aim of the upcoming Global Heat Flow Data Assessment Project, for which this data set provides the basis. Consequently, we kindly ask the user to take notice that the current release still suffers similar problems as previously published compilations in terms of data heterogeneity, documentation and quality.

This data publication contains the compilation of global heat-flow data by the International Heat Flow Commission (IHFC; http://www.ihfc-iugg.org/) of the International Association of Seismology and Physics of the Earth's Interior (IASPEI). The presented data release 2021 contains data generated between 1939 and 2021 and constitutes an updated and extended version of the 2012 IHFC database release (IHFC 2012; later re-published as PANGAEA release: Global Heat Flow Compilation Group, 2013). The 2021 release contains 74,548 heat-flow data from 1,403 publications. 55% of the reported heat-flow values are from the continental domain (n ~ 40,870), while the remaining 45% are located in the oceanic domain (n ~ 33,678). The data are provided in csv and Excel formats. Compared to earlier compilations, which followed the structure defined by Jessop et al. (1976), the new data release was transformed to the recently redefined structure for reporting and storing heat-flow data in the Global Heat Flow Database (Fuchs et al., 2021). Therefore, the notation and structure of the database was adopted, transforming the database field entries defined after Jessop et al. (1976) to the new field structure. Old code notations are not continued and the dataset was cleaned for entries without reporting any heat-flow value. Although successfully transformed, this release marks an intermediate step as the majority of the newly defined database fields have not been filled yet. Filling these fields, checking the existing entries and assessing the quality of each entry are the aim of the upcoming Global Heat Flow Data Assessment Project, for which this data set provides the basis. Consequently, we kindly ask the user to take notice that the current release still suffers similar problems as previously published compilations in terms of data heterogeneity, documentation and quality.

The prolonged COVID-19 pandemic has disrupted the TVET professional development training, which was planned to be carried out in a face-to-face manner. This study aims to examine TVET professional development training based on the ADDIE model and provide implications for ODA and TVET professional development training in the post-COVID era. In this case study, a TVET training program for Botswana was developed based on the ADDIE model in an untact environment. Accordingly, the performance activities for each phase of analysis, design, development, implementation, and evaluation were analyzed, and based on this, implications for ODA and TVET were provided. This study identified the applicability of non-face-to-face education in the ODA project. Also, this study explored how to develop systematic and dimensional programs based on the ADDIE model in a non-face-to-face manner. In addition, sustainability could be secured through cooperative partnerships between donor and beneficiary countries from the perspective of SDGs Goal.

The prolonged COVID-19 pandemic has disrupted the TVET professional development training, which was planned to be carried out in a face-to-face manner. This study aims to examine TVET professional development training based on the ADDIE model and provide implications for ODA and TVET professional development training in the post-COVID era. In this case study, a TVET training program for Botswana was developed based on the ADDIE model in an untact environment. Accordingly, the performance activities for each phase of analysis, design, development, implementation, and evaluation were analyzed, and based on this, implications for ODA and TVET were provided. This study identified the applicability of non-face-to-face education in the ODA project. Also, this study explored how to develop systematic and dimensional programs based on the ADDIE model in a non-face-to-face manner. In addition, sustainability could be secured through cooperative partnerships between donor and beneficiary countries from the perspective of SDGs Goal.

UnlabelledWe have developed a novel model for depleting mouse hepatic stellate cells (HSCs) that has allowed us to clarify their contributions to hepatic injury and fibrosis. Transgenic (Tg) mice expressing the herpes simplex virus thymidine kinase gene (HSV-Tk) driven by the mouse GFAP promoter were used to render proliferating HSCs susceptible to killing in response to ganciclovir (GCV). Effects of GCV were explored in primary HSCs and in vivo. Panlobular damage was provoked to maximize HSC depletion by combining CCl(4) (centrilobular injury) with allyl alcohol (AA) (periportal injury), as well as in a bile duct ligation (BDL) model. Cell depletion in situ was quantified using dual immunofluorescence (IF) for desmin and GFAP. In primary HSCs isolated from both untreated wild-type (WT) and Tg mice, GCV induced cell death in ≈ 50% of HSCs from Tg, but not WT, mice. In TG mice treated with CCl(4) +AA+GCV, there was a significant decrease in GFAP and desmin-positive cells, compared to WT mice (≈ 65% reduction; P < 0.01), which was accompanied by a decrease in the expression of HSC-activation markers (alpha smooth muscle actin, beta platelet-derived growth factor receptor, and collagen I). Similar results were observed after BDL. Associated with HSC depletion in both fibrosis models, there was marked attenuation of fibrosis and liver injury, as indicated by Sirius Red/Fast Green, hematoxylin and eosin quantification, and serum alanine/aspartate aminotransferase. Hepatic expression of interleukin-10 and interferon-gamma was increased after HSC depletion. No toxicity of GCV in either WT or Tg mice accounted for the differences in injury.ConclusionActivated HSCs significantly amplify the response to liver injury, further expanding this cell type's repertoire in orchestrating hepatic injury and repair.

Controlling the crystallographic structure in olivine lithium phosphates is crucial for obtaining superior electronic (J. Electrochem. Soc., 2002, 149, A1184-A1189) and ionic conductivities (Electrochem. Solid-State Lett., 2006, 9, A352-A355; Electrochem. Solid-State Lett., 2006, 9, A439-A442; Nat. Mater., 2002, 1, 123-128), and stability, for use as cathodes in lithium batteries. Here, we report a completely new approach to enhance Li+ extraction and transport in LiCoPO4 through Fe doping. We show that preferential Fe occupation of the 4c sites suppresses 4a–4c antisite mixing of Li and Co, thereby stabilizing the olivine structure by compensating for the Co-encapsulating oxygen octahedron shrinkage due to Co2+ oxidation during Li+ extraction. The structural stabilization gives rise to 10% higher charge capacity at a two-fold lower resistance than the undoped counterparts besides accelerating the intercalation/extraction kinetics. Our findings provide key atomistic-level insights that pave the way for the rational design and realization of new types of metal-doped cathode materials for lithium batteries and related applications.

Controlling the crystallographic structure in olivine lithium phosphates is crucial for obtaining superior electronic (J. Electrochem. Soc., 2002, 149, A1184-A1189) and ionic conductivities (Electrochem. Solid-State Lett., 2006, 9, A352-A355; Electrochem. Solid-State Lett., 2006, 9, A439-A442; Nat. Mater., 2002, 1, 123-128), and stability, for use as cathodes in lithium batteries. Here, we report a completely new approach to enhance Li+ extraction and transport in LiCoPO4 through Fe doping. We show that preferential Fe occupation of the 4c sites suppresses 4a–4c antisite mixing of Li and Co, thereby stabilizing the olivine structure by compensating for the Co-encapsulating oxygen octahedron shrinkage due to Co2+ oxidation during Li+ extraction. The structural stabilization gives rise to 10% higher charge capacity at a two-fold lower resistance than the undoped counterparts besides accelerating the intercalation/extraction kinetics. Our findings provide key atomistic-level insights that pave the way for the rational design and realization of new types of metal-doped cathode materials for lithium batteries and related applications.

Controlling the crystallographic structure in olivine lithium phosphates is crucial for obtaining superior electronic (J. Electrochem. Soc., 2002, 149, A1184-A1189) and ionic conductivities (Electrochem. Solid-State Lett., 2006, 9, A352-A355; Electrochem. Solid-State Lett., 2006, 9, A439-A442; Nat. Mater., 2002, 1, 123-128), and stability, for use as cathodes in lithium batteries. Here, we report a completely new approach to enhance Li+ extraction and transport in LiCoPO4 through Fe doping. We show that preferential Fe occupation of the 4c sites suppresses 4a–4c antisite mixing of Li and Co, thereby stabilizing the olivine structure by compensating for the Co-encapsulating oxygen octahedron shrinkage due to Co2+ oxidation during Li+ extraction. The structural stabilization gives rise to 10% higher charge capacity at a two-fold lower resistance than the undoped counterparts besides accelerating the intercalation/extraction kinetics. Our findings provide key atomistic-level insights that pave the way for the rational design and realization of new types of metal-doped cathode materials for lithium batteries and related applications.

Controlling the morphology and size of titanium dioxide (TiO2) nanostructures is crucial to obtain superior photocatalytic, photovoltaic, and electrochemical properties. However, the synthetic techniques for preparing such structures, especially those with complex configurations, still remain a challenge because of the rapid hydrolysis of Ti-containing polymer precursors in aqueous solution. Herein, we report a completely novel approach—three-dimensional (3D) TiO2 nanostructures with favorable dendritic architectures—through a simple hydrothermal synthesis. The size of the 3D TiO2 dendrites and the morphology of the constituent nano-units, in the form of nanorods, nanoribbons, and nanowires, are controlled by adjusting the precursor hydrolysis rate and the surfactant aggregation. These novel configurations of TiO2 nanostructures possess higher surface area and superior electrochemical properties compared to nanoparticles with smooth surfaces. Our findings provide an effective solution for the synthesis of complex TiO2 nano-architectures, which can pave the way to further improve the energy storage and energy conversion efficiency of TiO2-based devices.

Controlling the morphology and size of titanium dioxide (TiO2) nanostructures is crucial to obtain superior photocatalytic, photovoltaic, and electrochemical properties. However, the synthetic techniques for preparing such structures, especially those with complex configurations, still remain a challenge because of the rapid hydrolysis of Ti-containing polymer precursors in aqueous solution. Herein, we report a completely novel approach—three-dimensional (3D) TiO2 nanostructures with favorable dendritic architectures—through a simple hydrothermal synthesis. The size of the 3D TiO2 dendrites and the morphology of the constituent nano-units, in the form of nanorods, nanoribbons, and nanowires, are controlled by adjusting the precursor hydrolysis rate and the surfactant aggregation. These novel configurations of TiO2 nanostructures possess higher surface area and superior electrochemical properties compared to nanoparticles with smooth surfaces. Our findings provide an effective solution for the synthesis of complex TiO2 nano-architectures, which can pave the way to further improve the energy storage and energy conversion efficiency of TiO2-based devices.

Controlling the morphology and size of titanium dioxide (TiO2) nanostructures is crucial to obtain superior photocatalytic, photovoltaic, and electrochemical properties. However, the synthetic techniques for preparing such structures, especially those with complex configurations, still remain a challenge because of the rapid hydrolysis of Ti-containing polymer precursors in aqueous solution. Herein, we report a completely novel approach—three-dimensional (3D) TiO2 nanostructures with favorable dendritic architectures—through a simple hydrothermal synthesis. The size of the 3D TiO2 dendrites and the morphology of the constituent nano-units, in the form of nanorods, nanoribbons, and nanowires, are controlled by adjusting the precursor hydrolysis rate and the surfactant aggregation. These novel configurations of TiO2 nanostructures possess higher surface area and superior electrochemical properties compared to nanoparticles with smooth surfaces. Our findings provide an effective solution for the synthesis of complex TiO2 nano-architectures, which can pave the way to further improve the energy storage and energy conversion efficiency of TiO2-based devices.

Controlling the morphology and size of titanium dioxide (TiO2) nanostructures is crucial to obtain superior photocatalytic, photovoltaic, and electrochemical properties. However, the synthetic techniques for preparing such structures, especially those with complex configurations, still remain a challenge because of the rapid hydrolysis of Ti-containing polymer precursors in aqueous solution. Herein, we report a completely novel approach—three-dimensional (3D) TiO2 nanostructures with favorable dendritic architectures—through a simple hydrothermal synthesis. The size of the 3D TiO2 dendrites and the morphology of the constituent nano-units, in the form of nanorods, nanoribbons, and nanowires, are controlled by adjusting the precursor hydrolysis rate and the surfactant aggregation. These novel configurations of TiO2 nanostructures possess higher surface area and superior electrochemical properties compared to nanoparticles with smooth surfaces. Our findings provide an effective solution for the synthesis of complex TiO2 nano-architectures, which can pave the way to further improve the energy storage and energy conversion efficiency of TiO2-based devices.

Controlling the morphology and size of titanium dioxide (TiO2) nanostructures is crucial to obtain superior photocatalytic, photovoltaic, and electrochemical properties. However, the synthetic techniques for preparing such structures, especially those with complex configurations, still remain a challenge because of the rapid hydrolysis of Ti-containing polymer precursors in aqueous solution. Herein, we report a completely novel approach-three- dimensional (3D) TiO2 nanostructures with favorable dendritic architectures-through a simple hydrothermal synthesis. The size of the 3D TiO2 dendrites and the morphology of the constituent nano-units, in the form of nanorods, nanoribbons, and nanowires, are controlled by adjusting the precursor hydrolysis rate and the surfactant aggregation. These novel configurations of TiO2 nanostructures possess higher surface area and superior electrochemical properties compared to nanoparticles with smooth surfaces. Our findings provide an effective solution for the synthesis of complex TiO2 nano-architectures, which can pave the way to further improve the energy storage and energy conversion efficiency of TiO 2-based devices.

Controlling the morphology and size of titanium dioxide (TiO2) nanostructures is crucial to obtain superior photocatalytic, photovoltaic, and electrochemical properties. However, the synthetic techniques for preparing such structures, especially those with complex configurations, still remain a challenge because of the rapid hydrolysis of Ti-containing polymer precursors in aqueous solution. Herein, we report a completely novel approach—three-dimensional (3D) TiO2 nanostructures with favorable dendritic architectures—through a simple hydrothermal synthesis. The size of the 3D TiO2 dendrites and the morphology of the constituent nano-units, in the form of nanorods, nanoribbons, and nanowires, are controlled by adjusting the precursor hydrolysis rate and the surfactant aggregation. These novel configurations of TiO2 nanostructures possess higher surface area and superior electrochemical properties compared to nanoparticles with smooth surfaces. Our findings provide an effective solution for the synthesis of complex TiO2 nano-architectures, which can pave the way to further improve the energy storage and energy conversion efficiency of TiO2-based devices.

Controlling the crystallographic structure in olivine lithium phosphates is crucial for obtaining superior electronic (J. Electrochem. Soc., 2002, 149, A1184-A1189) and ionic conductivities (Electrochem. Solid-State Lett., 2006, 9, A352-A355; Electrochem. Solid-State Lett., 2006, 9, A439-A442; Nat. Mater., 2002, 1, 123-128), and stability, for use as cathodes in lithium batteries. Here, we report a completely new approach to enhance Li+ extraction and transport in LiCoPO4 through Fe doping. We show that preferential Fe occupation of the 4c sites suppresses 4a–4c antisite mixing of Li and Co, thereby stabilizing the olivine structure by compensating for the Co-encapsulating oxygen octahedron shrinkage due to Co2+ oxidation during Li+ extraction. The structural stabilization gives rise to 10% higher charge capacity at a two-fold lower resistance than the undoped counterparts besides accelerating the intercalation/extraction kinetics. Our findings provide key atomistic-level insights that pave the way for the rational design and realization of new types of metal-doped cathode materials for lithium batteries and related applications.