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We have entered the Fourth Industrial Revolution, which has brought widespread digital transformation with advanced and broadened technologies including artificial intelligence (AI). To help students prosper in a world full of AI applications, it is important for us to offer students sufficient AI-integrated learning opportunities across different subjects, including science. In this position paper, a pedagogical approach to AI-integrated science education through facilitating epistemic discourse is proposed. To establish a foundation for this integration, epistemic similarities and differences between how scientific knowledge is constructed and how AI agents learn are compared, referring to Chinn et al.’s (2014) epistemic cognition framework that attends to epistemic aims, ideals, and processes. Four bins of instructional strategies for facilitating epistemic discourse in AI-integrated science classrooms is suggested, which will help students more readily act as informed knowledge constructors, critics, and users of AI and science, who can pose questions that matter to their lives.

Hyperbilirubinemia is the most common neonatal disease and is observed in about 80% of newborns worldwide in neonatal period within a week after birth. Untreated infant hyperbilirubinemia may lead to brain damage and even death, so it is very important to diagnose it quickly and accurately. In this study, a total bilirubin measurement system was developed that is portable and easy to use without pre-processing using a commercial smartphone. This system measures using the LED and camera of the smartphone without the need for additional devices, and because a small amount of blood is injected without pre-treatment, anyone can easily measure it in the field. In a comparative study with Cobas c111 results, accuracy meets CLIA guidelines with 94% (17/18) within ±0.4 mg/dL below 3 mg/dL and 98% within ±20% above 3 mg/dL (276/282). This system offers a simple, fast and accurate diagnosis for jaundice in infants and young children in low-resource settings.

SYNOPSIS The purpose of this paper is to encourage and support academic research related to U.S. state and local government financial reporting. We provide an overview of U.S. state and local governments and their financial reporting, discuss sources of government data available to researchers, review key streams of academic research on governmental financial reporting, and suggest opportunities for future research in this area. JEL Classifications: H50; H70; H71; H72; H83; M41; M48.

Science textbooks, as one of the main tools for school science education, contain knowledge and practices valued by Western epistemological culture. As those who (will) live in a world expanding fr...

Extracellular vesicles (EVs) are cell derivatives containing diverse cellular molecules, have various physiological properties and are also present in stem cells used for regenerative therapy. We selected a “multiplexed target” that demonstrates multiple effects on various cardiovascular cells, while functioning as a cargo of EVs. We screened various microRNAs (miRs) and identified miR-210 as a candidate target for survival and angiogenic function. We confirmed the cellular and biological functions of EV-210 (EVs derived from ASCmiR-210) secreted from adipose-derived stem cells (ASCs) transfected with miR-210 (ASCmiR-210). Under hypoxic conditions, we observed that ASCmiR-210 inhibits apoptosis by modulating protein tyrosine phosphatase 1B (PTP1B) and death-associated protein kinase 1 (DAPK1). In hypoxic endothelial cells, EV-210 exerted its angiogenic capacity by inhibiting Ephrin A (EFNA3). Furthermore, EV-210 enhanced cell survival under the control of PTP1B and induced antiapoptotic effects in hypoxic H9c2 cells. In cardiac fibroblasts, the fibrotic ratio was reduced after exposure to EV-210, but EVs derived from ASCmiR-210 did not communicate with fibroblasts. Finally, we observed the functional restoration of the ischemia/reperfusion-injured heart by maintaining the intercommunication of EVs and cardiovascular cells derived from ASCmiR-210. These results suggest that the multiplexed target with ASCmiR-210 is a useful tool for cardiovascular regeneration., Heart disease: Boosting microRNA activity may restore heart function A therapy designed to enhance the activity of a small regulatory RNA molecule could prompt the restoration of cellular communication and improve heart function during heart disease. Heart cells struggle to function and regenerate under the reduced oxygen conditions caused by narrowed or blocked blood vessels. Stem cell-derived therapies may restore damaged heart tissues, and can be designed to secrete specific factors that boost regeneration. To identify factors that may improve heart recovery chances, Woochul Chang at Pusan National University, Busan, Korea and co-workers examined stem cell-derived extracellular vesicles (EVs), cellular membrane sacs that carry proteins and RNAs to surrounding tissues and boost intercellular communication. The team identified microRNA-210 as a key factor that inhibits heart cell death, reduces fibrosis, and enhances regeneration of heart cell populations. EVs secreting microRNA-210 may prove a useful therapeutic tool.

Addressing ways in which systemic injustices manifest in learning environments has been a significant challenge to the field of informal science learning (ISL). The dominant discourses of equity are framed around calls for inclusion and the extension of rights for quality learning opportunities for all youth. In this paper, we move beyond inclusionary approaches to use the justice-oriented framework of rightful presence. Grounded in participatory design research, the findings show how possibilities for rightful presence arise when educators and youths collaboratively engage in exposing, disrupting, and transforming unjust narratives and practices that position youths as knowledge recipients and temporary guests in the host ISL institutions. These possibilities are characterized by opportunities to foreground youths’ lived lives and community wisdom in ways that shift the boundaries of who and what science is for. We discuss insights, dilemmas, and implications regarding justice-oriented pedagogies and their possibilities for rightful presence in science education.

An amphipathic PAA-POSS@DOX drug delivery system that responds sensitively to pH changes in the cancer microenvironment has been developed using a nanoparticle based on inorganic polyhedral oligomeric silsesquioxane (POSS). POSS was introduced to the carboxylic acid group of polyacrylic acid to which doxorubicin anticancer drug was loaded to prepare 480 ± 192 nm self-assembled nanoparticles. PAA-POSS had a high loading efficiency of over 75% and doxorubicin was quickly released to the target area responding sensitively to weakly acidic conditions. The possibility of employing PAA-POSS as a targeted drug delivery system has been confirmed by observing the death of cells of the MDA-MB-231 breast cancer line.

Self-regulated “smart” insulin administration system that mimic pancreatic endocrine function would be highly desirable for diabetes management. Here, a glucose-responsive continuous insulin delivery system is developed, where novel polyhedral oligosilsesquioxane (POSS) modified with 3‐aminophenylboronic acid (APBA) were used to encapsulate insulin (insulin entrapment efficiency: 73.2%) to prepare a fast response, high stability, good distribution, and excellent biocompatible system. Due to the strong hydrophobicity of POSS, the POSS moiety is located at the core in aqueous solution and combines with the boronic group of APBA and the diol generated in PEG-insulin to form a nanomicelle structure, that is, nanoparticles naturally. Micelles self‐assembled from these molecules possess glucose‐responsiveness at varying glucose concentrations. The interaction of the PBA and diol containing insulin via boronate ester bond and its interchange with glucose was investigated by FT-IR, 1H NMR and XPS. Furthermore, the successful glucose-triggered release of insulin from the POSS-APBA micelles was investigated at neutral pH. A linear graph was plotted with the measured released insulin vs glucose concentrations, with a linear correlation coefficient (R2) value close to 1. Circular dichroism (CD) spectroscopy analysis was performed to measure insulin activity by comparing secondary structures of insulin, PEG-Insulin, and POSS-APBA@insulin. When confirming intracellular apoptosis signaling, cleaved caspase 3 and caspase 9 were not increased by 640 μg/ml POSS-APBA and POSS-APBA@insulin in HeLa, HDF and HUVE cells. Application in the biomedical field for controlled delivery of insulin appear to be promising.

In this chapter, we explore how Olga, her partner educators and researchers, and youth re-imagined their science museum through a research-practice partnership (RPP) initiated in 2015. Initially formed to design a maker space, over time, the RPP enacted these imaginaries, which altered both the space of the science museum and how we related to the space. We share how our RPP team co-produced new and more just spatial imaginaries in/for the science museum through both transforming discourses (i.e., how we talked about what science is, who can do science, and where science happens in relation to our lives as it is taken up and represented in the Center) and transforming practices (i.e., the practices we collectively took up to enact these discourses toward altering the spaces of the Center). These transforming discourses and practices helped to make visible the histories and present of youths’ lived lives and created foundations upon which the RPP could organize for justice-oriented action. We share three vignettes to explore the co-production of spatial imaginaries for reclaiming the Center. Across these vignettes, we illustrate how youth took up familiar spaces in new and multimodal ways through their discourses and practices.

In order to make informed decisions about socioscientific issues (SSIs), people must evaluate the trustworthiness of associated knowledge claims. In this chapter, we apply Duncan et al.’s (J Res Sci Teach 55(7):907–937, 2018) Grasp of Evidence (GOE) framework to empirical data. We analysed scenario-based interviews in which 15 undergraduate students evaluated SSI-related scientific knowledge claims to make hypothetical decisions. Based on a content analysis of these interviews, we illustrate the utility of the GOE framework for distinguishing between understandings of experts’ and laypeople’s use of evidence and among understandings of different evidentiary practices used by experts. Through grounded theory analysis in parallel with concurrent review of relevant literature, we further identified epistemic concepts that seemed to underlie students’ GOE and to account for meaningful differences in their evaluations of SSI-related knowledge claims. We discuss implications of these findings for researchers and science educators.

In the chemical mechanical polishing process of semiconductor manufacturing, the concentration of ‘large’ particles (\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\ge $$\end{document}≥0.5 μm) in the slurry, which is considerably larger in size than the main abrasives (\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\approx $$\end{document}≈ 0.1 μm), is a critical parameter that strongly influences manufacturing defects, yields, and reliabilities of large-scale-integrated circuits. Various instruments, so-called particle counters, based on light scattering, light extinction, and holography techniques have been developed to measure and monitor the large particle concentration in semiconductor fabs in real time. However, sizeable fluctuation in the measured particle concentration complicates the statistical process control in the fabs worldwide. Here, we show that an inherent fluctuation exists in the counting of large particles, which is universal, independent of instrument type, and quantitatively determined by the instrument’s operation parameters. We analytically derive a statistical theory of the fluctuation based on Poisson statistics and validate the theory through experiments and Monte-Carlo simulation. Furthermore, we provide a strategy to enhance the measurement accuracy by statistically adjusting the instrumental parameters commonly involved in the particle counters. The present results and analyses could be useful for statistical process control in semiconductor fabs to prevent large particle-induced defects such as micro-scratches and pits on wafers.

Macrophages are re-educated and polarized in response to myocardial infarction (MI). The M2 anti-inflammatory phenotype is a known dominator of late stage MI. Mesenchymal stem cells (MSCs) represent a promising tool for cell therapy, particularly heart related diseases. In general, MSCs induce alteration of the macrophage subtype from M1 to M2, both in vitro and in vivo. We conjectured that hypoxic conditions can promote secretome productivity of MSCs. Hypoxia induces TGF-β1 expression, and TGF-β1 mediates M2 macrophage polarization for anti-inflammation and angiogenesis in infarcted areas. We hypothesized that macrophages undergo advanced M2 polarization after exposure to MSCs in hypoxia. Treatment of MSCs derived hypoxic conditioned medium (hypo-CM) promoted M2 phenotype and neovascularization through the TGF-β1/Smad3 pathway. In addition, hypo-CM derived from MSCs improved restoration of ischemic heart, such as attenuating cell apoptosis and fibrosis, and ameliorating microvessel density. Based on our results, we propose a new therapeutic method for effective MI treatment using regulation of macrophage polarization. [BMB Reports 2020; 53(11): 600-604].

Room-temperature fabrication of TiO2/Cu composite films for embedded passive components were attempted via aerosol deposition process. XRD analysis and observation of internal microstructures revealed that TiO2/Cu composite films using 500 nm-sized TiO2 had further tight bonding between particles compared to 25 nm-sized TiO2, due to effect of initial TiO2 particle size on densification of internal microstructures. Then, to optimize their adhesive strength and temperature coefficient of resistance (TCR), electrical and mechanical properties of TiO2 (500 nm)/Cu composite films with different content of TiO2 were evaluated for applications as advanced composite film resistors. Results showed that TiO2/Cu (50 wt%/50 wt%) composite films had sufficient electrical resistivity (5.8 ×10−3 Ω cm), excellent near-zero TCR (−3 ppm/℃), and improved adhesive strength (~ 7.37 N/mm2) resulting from proper coexistence of anchoring bonds and mechanical interlocking formed during deposition.

Exosomes are small membranous vesicles which contain abundant RNA molecules, and are transferred from releasing cells to uptaking cells. MicroRNA (miRNA) is one of the transferred molecules affecting the adopted cells, including glioma cells. We hypothesized that mesenchymal stem cells (MSCs) can secrete exosomes loading miRNA and have important effects on the progress of gliomas. To determine these effects by treating exosomal miRNA in culture media of miRNA mimic transfected MSCs, we assessed the in vitro cell proliferation and invasion capabilities, and the expression level of relative proteins associated with cell apoptosis, growth and migration. For animal studies, the mice injected with U87 cells were exposed to exosomes derived from miRNA-584-5p transfected MSCs, to confirm the influence of exosomal miRNA on the progress of glioma. Based on our results, we propose a new targeted cancer therapy wherein exosomes derived from miRNA transfected MSCs could be used to modulate tumor progress as the anticancer vehicles. [BMB Reports 2018; 51(8): 406-411].

Light-emitting diodes (LEDs) have been widely applied for backlight unit for displays, general lighting, and automotive illumination because they have a high light efficiency and long life time, and are environmentally friendly. These diverse applications require smaller and slim LED chip scale packages (CSPs). CSP LEDs have been developed to produce white LED chips by forming a thin phosphor film on blue LED chips. In this study, we investigated the effect of phosphor layer thickness and area on the optical and thermal properties of the CSP LEDs. The phosphor-conversion of chips is maximized by varying the thickness and area of the phosphor layer. Eight different types of phosphor-converted white CSPs with normal performance (CRI > 70, CCT ~ 5700 K) were prepared by using mixed multicolor phosphor materials. In other words, for five samples whose CSP area was fixed at 1.8 x 1.8 mm2, flip-chip area was 1.4 x 1.4 mm2, and flip-chip thickness was 250 μm, the thickness of the phosphor layers was varied from 100 to 500 μm at intervals of 100 μm. For other three samples where the phosphor layer thickness was fixed at 300 μm, the flip-chip area was 1.4 x 1.4 mm2, and flip-chip thickness was 250 μm, the CSPs had three different areas of 1.6 x 1.6, 1.8 x 1.8, and 2.0 x 2.0 mm2. First, the relative luminous flux and LED beam distribution were characterized using integrating sphere and a goniometer. It was shown that as the thickness of the phosphor layer increased, the luminous flux and the directivity angle increased. On the other hand, as the CSP area increased, the luminous flux and the directivity angle decreased. This could be attributed to the fact that CSP does not have a reflector (namely, a housing material) and so the blue light of the chip does not excite the whole area of the phosphor. This may be confirmed by the images showing light distribution and luminescence characteristics, which is currently under investigation. Furthermore, a junction temperature measurement system was used to characterize the junction temperatures of the five different samples whose phosphor layer thicknesses were varied from 100 to 500 μm. It was found that when the thickness of the phosphor layer exceeded the thickness of the chips (250 μm), the junction temperature of the samples dramatically increased. Further details regarding the phosphor layer thickness of the junction temperature characteristics will be investigated and described.

The performance of glucose sensors based on non-enzymatic receptors is often limited because of the aggregation of receptors and the resulting lowered binding efficiency. To improve the limit of detection (LOD) in glucose sensors, a polyoligomeric silsesquioxane (POSS) is introduced as a support to enhance the binding efficiency between glucose and non-enzymatic receptor. POSS support reduces the aggregation and partially grants orientation to ensure that non-enzymatic receptors can productively react with targets. The synthesized amine@POSS-aminophenylboronic acid (APBA) conjugate was immobilized on the surface of gold nanoparticles, which were fastened on the optical fiber. Optical fiber-based sensors using localized surface plasmon resonance (LSPR) enabled rapid detection, ease of handling, and remote sensing. After confirming the response characteristics to the refractive index, a suitable concentration of amine@POSS-APBA receptor was selected for the fabricated fiber optic sensor. Glucose detection was performed at various concentrations using non-enzymatic receptors with and without POSS support. The experimental results demonstrated that increased responses were observed in the designed method than when only the non-enzymatic receptor was applied. The LOD for glucose was quantified as 25.0 μM. We believe that improved glucose sensors based on fiber optic LSPR and POSS support has the potential to be applied to field detection in various fields, such as medicine, food safety, and the environment.

Lysine-specific demethylase 1 (LSD1) has become a biologically important and validated epigenetic target for cancer therapy since its identification in 2004. LSD1 mediates many cellular signaling pathways and is involved in the initiation and development of cancers. Aberrant overexpression of LSD1 has been observed in different types of cancers, and such epigenetic dysregulation plays a critical role in pathogenesis of various types of cancers such as acute myeloid leukemia (AML) or small cell lung cancer (SCLC). In this study, we introduce HM97346 and its derivatives as novel LSD1 inhibitors, and report a therapeutic potential for AML and SCLC patients based on several preclinical characterization and assessment. HM97346 and its derivatives were designed and synthesized as novel reversible inhibitors of LSD1. Standard cell proliferation assay, immunoblotting, biomarker expression, and apoptosis analysis were carried out to validate their potency in vitro studies using different AML and SCLC cell lines. The in vivo antitumor activity was evaluated in AML and SCLC cell xenograft mouse models. Tumor sizes were measured and tumor samples were analyzed to define the mechanisms of action. HM97346 and its derivatives showed strong inhibition on LSD1 enzymatic activity in biochemical assay and promoted the methylations of histone H3 lysine 4 (H3K4) in both SCLC and AML cells. They reduced the expression of neuroendocrine factors ASCL1 in SCLC cells, effectively and dose-dependently. Moreover, in human AML cell lines, they stimulated cellular differentiation by disrupting LSD1-GFI1 complex and induced transcription factor PU.1 as well as myeloid differentiation markers CD86 and CD11b. As a result, they significantly inhibited cellular proliferation and induced apoptosis in studies using AML and SCLC cells. Oral administration of HM97346 and its derivatives inhibited tumor growth in human AML and SCLC cell xenograft mouse models studies. These antitumor effects dramatically increased in combination with standard chemotherapies. In conclusion, HM97346 and its derivatives, new synthesized reversible LSD1 inhibitors, showed potential anticancer activity in preclinical AML and SCLC models. Moreover, these compounds could provide a new insight and possibility in cancer therapy through epigenetic modulation as not only monotherapy but also combination therapy. Citation Format: Joo-Yun Byun, Won Jong Lee, Won jung Kim, Minjeong Kim, Inhwan Bae, Seokhyun Hong, Yu-Yon Kim, Hyunjin Park, Eunyoung Kim, Young Hoon Kim, Young Gil Ahn, Kwee Hyun Suh. Antitumor activity of novel reversible LSD1 inhibitors in preclinical models of AML and SCLC [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 1135.