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1.
PLoS One ; 19(4): e0302406, 2024.
Article in English | MEDLINE | ID: mdl-38635551

ABSTRACT

Natural killer (NK) cells play a crucial role in immunosurveillance independent of antigen presentation, which is regulated by signal balance via activating and inhibitory receptors. The anti-tumor activity of NK cells is largely dependent on signaling from target recognition to cytolytic degranulation; however, the underlying mechanism remains unclear, and NK cell cytotoxicity is readily impaired by tumor cells. Understanding the activation mechanism is necessary to overcome the immune evasion mechanism, which remains an obstacle in immunotherapy. Because calcium ions are important activators of NK cells, we hypothesized that electrical stimulation could induce changes in intracellular Ca2+ levels, thereby improving the functional potential of NK cells. In this study, we designed an electrical stimulation system and observed a correlation between elevated Ca2+ flux induced by electrical stimulation and NK cell activation. Breast cancer MCF-7 cells co-cultured with electrically stimulated KHYG-1 cells showed a 1.27-fold (0.5 V/cm) and 1.55-fold (1.0 V/cm) higher cytotoxicity, respectively. Electrically stimulated KHYG-1 cells exhibited a minor increase in Ca2+ level (1.31-fold (0.5 V/cm) and 1.11-fold (1.0 V/cm) higher), which also led to increased gene expression of granzyme B (GZMB) by 1.36-fold (0.5 V/cm) and 1.58-fold (1.0 V/cm) by activating Ca2+-dependent nuclear factor of activated T cell 1 (NFAT1). In addition, chelating Ca2+ influx with 5 µM BAPTA-AM suppressed the gene expression of Ca2+ signaling and lytic granule (granzyme B) proteins by neutralizing the effects of electrical stimulation. This study suggests a promising immunotherapeutic approach without genetic modifications and elucidates the correlation between cytolytic effector function and intracellular Ca2+ levels in electrically stimulated NK cells.


Subject(s)
Calcium , Neoplasms , Humans , Granzymes/metabolism , Calcium/metabolism , Killer Cells, Natural , Lymphocyte Activation , Neoplasms/metabolism , Cytotoxicity, Immunologic
2.
Bioengineering (Basel) ; 10(12)2023 Dec 15.
Article in English | MEDLINE | ID: mdl-38136019

ABSTRACT

Non-contact remote photoplethysmography can be used in a variety of medical and healthcare fields by measuring vital signs continuously and unobtrusively. Recently, end-to-end deep learning methods have been proposed to replace the existing handcrafted features. However, since the existing deep learning methods are known as black box models, the problem of interpretability has been raised, and the same problem exists in the remote photoplethysmography (rPPG) network. In this study, we propose a method to visualize temporal and spectral representations for hidden layers, deeply supervise the spectral representation of intermediate layers through the depth of networks and optimize it for a lightweight model. The optimized network improves performance and enables fast training and inference times. The proposed spectral deep supervision helps to achieve not only high performance but also fast convergence speed through the regularization of the intermediate layers. The effect of the proposed methods was confirmed through a thorough ablation study on public datasets. As a result, similar or outperforming results were obtained in comparison to state-of-the-art models. In particular, our model achieved an RMSE of 1 bpm on the PURE dataset, demonstrating its high accuracy. Moreover, it excelled on the V4V dataset with an impressive RMSE of 6.65 bpm, outperforming other methods. We observe that our model began converging from the very first epoch, a significant improvement over other models in terms of learning efficiency. Our approach is expected to be generally applicable to models that learn spectral domain information as well as to the applications of regression that require the representations of periodicity.

3.
Sci Rep ; 11(1): 7267, 2021 03 31.
Article in English | MEDLINE | ID: mdl-33790394

ABSTRACT

Although immunotherapy holds promising cytotoxic activity against lymphoma or leukemia, the immunosuppressive mechanisms of solid tumors remain challenging. In this study, we developed and applied a hypergravity exposure system as a novel strategy to improve the responsiveness of breast cancer cells to natural killer (NK) cells for efficient immunotherapy. Following exposure to hypergravity, either in the presence or absence of NK cells, we investigated for changes in the cell cytoskeletal structure, which is related to the F-actin mediated immune evasion mechanism (referred to as "actin response") of cancer cells. Breast cancer cell line MDA-MB-231 cells were exposed thrice to a 20 min hypergravitational condition (10 × g), with a 20 min rest period between each exposure. The applied hypergravity induces changes in the intracellular cytoskeleton structure without decreasing the cell viability but increasing the cytotoxicity of MDA-MB-231 from 4 to 18% (4.5-fold) at a 3:1 ratio (NK-to-target). Analyses related to F-actin further demonstrate that the applied hypergravity results in rearrangement of the cytoskeleton, leading to inhibition of the actin response of MDA-MB-231. Taken together, our results suggest that the mechanical load increases through application of hypergravity, which potentially improves efficiency of cell-based immunotherapies by sensitizing tumors to immune cell-mediated cytotoxicity.


Subject(s)
Actins/immunology , Breast Neoplasms/immunology , Hypergravity , Killer Cells, Natural/immunology , Neoplasm Proteins/immunology , Breast Neoplasms/therapy , Cytoskeleton/immunology , Female , Humans , Immunotherapy , MCF-7 Cells , Tumor Escape
4.
J Nanosci Nanotechnol ; 16(5): 4808-13, 2016 May.
Article in English | MEDLINE | ID: mdl-27483826

ABSTRACT

The effects of dry cleaning of a HfO2 gate stack using NF3 only and a NF3/NH3 gas mixture plasma were investigated. The plasma dry cleaning process was carried out after HfO2 deposition using an indirect down-flow capacitively coupled plasma (CCP) system. An analysis of the chemical composition of the HfO2 gate stacks by XPS indicated that fluorine was incorporated into the HfO2 films during the plasma dry cleaning. Significant changes in the HfO2 chemical composition were observed as a result of the NF3 dry cleaning, while they were not observed in this case of NF3/NH3 dry cleaning. TEM results showed that the interfacial layer (IL) between the HfO2 and Si thickness was increased by the plasma dry cleaning. However, in the case of NF3/NH3 dry cleaning using 150 W, the IL thickness was suppressed significantly compared to the sample that had not been dry cleaned. Its electrical properties were also improved, including the low gate leakage currents, and reduced EOT. Finally, the finding show that the IL thickness of the HfO2 gate stack can be controlled by using the novel NF3/NH3 dry cleaning process technique without any the significant changes in chemical composition and metal-oxide-semiconductor (MOS) capacitor characteristics.

5.
Mol Cells ; 39(2): 141-8, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26743902

ABSTRACT

Oriental melon (Cucumis melo L. var. makuwa) is one of six subspecies of melon and is cultivated widely in East Asia, including China, Japan, and Korea. Although oriental melon is economically valuable in Asia and is genetically distinct from other subspecies, few reports of genome-scale research on oriental melon have been published. We generated 30.5 and 36.8 Gb of raw RNA sequence data from the female and male flowers, leaves, roots, and fruit of two oriental melon varieties, Korean landrace (KM) and Breeding line of NongWoo Bio Co. (NW), respectively. From the raw reads, 64,998 transcripts from KM and 100,234 transcripts from NW were de novo assembled. The assembled transcripts were used to identify molecular markers (e.g., single-nucleotide polymorphisms and simple sequence repeats), detect tissue-specific expressed genes, and construct a genetic linkage map. In total, 234 single-nucleotide polymorphisms and 25 simple sequence repeats were screened from 7,871 and 8,052 candidates, respectively, between the KM and NW varieties and used for construction of a genetic map with 94 F2 population specimens. The genetic linkage map consisted of 12 linkage groups, and 248 markers were assigned. These transcriptome and molecular marker data provide information useful for molecular breeding of oriental melon and further comparative studies of the Cucurbitaceae family.


Subject(s)
Cucumis melo/genetics , Genome, Plant , Microsatellite Repeats , Polymorphism, Single Nucleotide , Transcriptome , Chromosome Mapping , Cucumis melo/classification , Flowers/genetics , Fruit/genetics , Gene Expression Profiling , Genetic Linkage , Plant Leaves/genetics , Plant Roots/genetics , Sequence Analysis, DNA
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