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  • 1
    In: Cancers, MDPI AG, Vol. 14, No. 16 ( 2022-08-11), p. 3887-
    Abstract: Cancer cells communicate with each other via exosomes in the tumor microenvironment. However, measuring trace amounts of proteins in exosomes is difficult, and thus the cancer stemness-promoting mechanisms of exosomal proteins have not been elucidated. In the present study, we attempted to quantify trace amounts of 78-kDa glucose-regulated protein (GRP78), which is involved in cancer progression, in exosomes released from cultured gastric cancer cells using an ultrasensitive ELISA combined with thio-NAD cycling. We also evaluated the cancer stemness-promoting effects by the application of high-GRP78-containing exosomes to cultured gastric cancer cells. The ultrasensitive ELISA enabled the detection of GRP78 at a limit of detection of 0.16 pg/mL. The stemness of cancer cultured cells incubated with high-GRP78-containing exosomes obtained from GRP78-overexpressed cells was increased on the basis of both an MTT assay and a wound healing assay. Our results demonstrated that the ultrasensitive ELISA has strong potential to measure trace amounts of proteins in exosomes. Further, exosomes with a high concentration of GRP78 promote the cancer stemness of surrounding cells. The technique for quantifying proteins in exosomes described here will advance our understanding of cancer stemness progression via exosomes.
    Type of Medium: Online Resource
    ISSN: 2072-6694
    Language: English
    Publisher: MDPI AG
    Publication Date: 2022
    detail.hit.zdb_id: 2527080-1
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  • 2
    In: Current Issues in Molecular Biology, MDPI AG, Vol. 44, No. 12 ( 2022-12-06), p. 6145-6157
    Abstract: Exosomes containing glucose-regulated protein 78 (GRP78) are involved in cancer malignancy. GRP78 is thought to promote the tumor microenvironment, leading to angiogenesis. No direct evidence for this role has been reported, however, mainly because of difficulties in accurately measuring the GRP78 concentration in the exosomes. Recently, exosomal GRP78 concentrations were successfully measured using an ultrasensitive ELISA. In the present study, GRP78 concentrations in exosomes collected from gastric cancer AGS cells with overexpression of GRP78 (OE), knockdown of GRP78 (KD), or mock GRP78 (mock) were quantified. These three types of exosomes were then incubated with vascular endothelial cells to examine their effects on endothelial cell angiogenesis. Based on the results of a tube formation assay, GRP78-OE exosomes accelerated angiogenesis compared with GRP78-KD or GRP78-mock exosomes. To investigate the mechanisms underlying this effect, we examined the Ser473 phosphorylation state ratio of AKT, which is involved in the angiogenesis process, and found that AKT phosphorylation was increased by GRP78-OE exosome application to the endothelial cells. An MTT assay showed that GRP78-OE exosome treatment increased the proliferation rate of endothelial cells, and a wound healing assay showed that this treatment increased the migration capacity of the endothelial cells. These findings demonstrated that GRP78-containing exosomes promote the tumor microenvironment and induce angiogenesis.
    Type of Medium: Online Resource
    ISSN: 1467-3045
    Language: English
    Publisher: MDPI AG
    Publication Date: 2022
    detail.hit.zdb_id: 2090836-2
    SSG: 12
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  • 3
    In: International Journal of Molecular Sciences, MDPI AG, Vol. 22, No. 7 ( 2021-03-31), p. 3614-
    Abstract: Atractylodin (ATR) is a bioactive component found in dried rhizomes of Atractylodes lancea (AL) De Candolle. Although AL has accumulated empirical evidence for the treatment of pain, the molecular mechanism underlying the anti-pain effect of ATR remains unclear. In this study, we found that ATR increases transient receptor potential ankyrin-1 (TRPA1) single-channel activity in hTRPA1 expressing HEK293 cells. A bath application of ATR produced a long-lasting calcium response, and the response was completely diminished in the dorsal root ganglion neurons of TRPA1 knockout mice. Intraplantar injection of ATR evoked moderate and prolonged nociceptive behavior compared to the injection of allyl isothiocyanate (AITC). Systemic application of ATR inhibited AITC-induced nociceptive responses in a dose-dependent manner. Co-application of ATR and QX-314 increased the noxious heat threshold compared with AITC in vivo. Collectively, we concluded that ATR is a unique agonist of TRPA1 channels, which produces long-lasting channel activation. Our results indicated ATR-mediated anti-nociceptive effect through the desensitization of TRPA1-expressing nociceptors.
    Type of Medium: Online Resource
    ISSN: 1422-0067
    Language: English
    Publisher: MDPI AG
    Publication Date: 2021
    detail.hit.zdb_id: 2019364-6
    SSG: 12
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  • 4
    Online Resource
    Online Resource
    MDPI AG ; 2023
    In:  Journal of Nuclear Engineering Vol. 4, No. 1 ( 2023-01-20), p. 154-164
    In: Journal of Nuclear Engineering, MDPI AG, Vol. 4, No. 1 ( 2023-01-20), p. 154-164
    Abstract: The mechanical consequences of core disruptive accidents (CDAs) are a major safety concern in sodium-cooled fast reactors. Once core disruption occurs, liquefied core materials rapidly disperse vertically and radially. The dispersed materials penetrate the pin bundles and control rod guide tubes (CRGTs) before freezing at the edge of the penetration zone as heat is transferred to surrounding structures. Such freezing phenomena can suppress the negative reactivity feedback of fuel dispersion. The discharge of core materials can be impeded, resulting in a molten core pool formation when tight blockages occur inside CRGTs due to frozen material. Accordingly, freezing phenomena of core materials play a key role in governing the mechanical consequences of a CDA. To validate a freezing model implemented in our CDA analysis code, ASTERIA-SFR, a preliminary simulation of the THEFIS RUN#1 test, was performed. The calculation results show that freezing on the structural wall and crust formation were key phenomena affecting the penetration behavior, and the structural heat transfer is an important parameter. A remarkable reduction of the heat transfer coefficient was required to reproduce the penetration length observed in the experiment. This suggests that the momentum exchange and flow regime at the leading edge as well as heat transfer should be well modeled to predict the freezing phenomena in rapidly evolving CDAs.
    Type of Medium: Online Resource
    ISSN: 2673-4362
    Language: English
    Publisher: MDPI AG
    Publication Date: 2023
    detail.hit.zdb_id: 3040700-X
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