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허남칠,김선민,박은령,박평심,김경수,이명렬 조선대학교 기초과학연구소 1998 自然科學硏究 Vol.21 No.1
This study was designed to investigate the free amino acid compositions of salt-fermented fish products in the markets of Chonnam area. The results were as follows : The free amino acid compositions of salt-fermented fish products had varying figures according to the species of raw materials, that is, lysine and leucine were relatively abundant in Myul-chi jeot (salt-fermented anchovy), arginine inSae-woo jeot (salt-fermented small shrimp), glutamic acid inJa-oi jeot (salt-fermented small shrimp). lysine, arginine, alanine and phenylalanine in To-h jeot (salt-fermented trout), etc. Essential amino acid contents were contained 31.02%∼83.46% of total amino acids in all sample, and lysine and leucine were most abundant among essential amino acids. Especially tryptophan was the richest in Cham-jo-gae jeot, phenylalanine in To-ha jeot, Kal-chi-nae-jang jeot and Song-eo jeot in other essential amino acids. because the degree of protein degradation wouldl be influenced on fermentation periods, salt-concentration, fermentation temperature, etc, we expected more systemic research by some varied conditions and the developed analytical techniques on the salt-fermented fish products should be followed.
S6K1 Negatively Regulates TAK1 Activity in the Toll-Like Receptor Signaling Pathway
Kim, So Yong,Baik, Kyung-Hwa,Baek, Kwan-Hyuck,Chah, Kyong-Hwa,Kim, Kyung Ah,Moon, Gyuyoung,Jung, Eunyu,Kim, Seong-Tae,Shim, Jae-Hyuck,Greenblatt, Matthew B.,Chun, Eunyoung,Lee, Ki-Young American Society for Microbiology 2014 Molecular and cellular biology Vol.34 No.3
<P>Transforming growth factor β (TGF-β)-activated kinase 1 (TAK1) is a key regulator in the signals transduced by proinflammatory cytokines and Toll-like receptors (TLRs). The regulatory mechanism of TAK1 in response to various tissue types and stimuli remains incompletely understood. Here, we show that ribosomal S6 kinase 1 (S6K1) negatively regulates TLR-mediated signals by inhibiting TAK1 activity. S6K1 overexpression causes a marked reduction in NF-κB and AP-1 activity induced by stimulation of TLR2 or TLR4. In contrast, S6K1<SUP>−/−</SUP> and S6K1 knockdown cells display enhanced production of inflammatory cytokines. Moreover, S6K1<SUP>−/−</SUP> mice exhibit decreased survival in response to challenge with lipopolysaccharide (LPS). We found that S6K1 inhibits TAK1 kinase activity by interfering with the interaction between TAK1 and TAB1, which is a key regulator protein for TAK1 catalytic function. Upon stimulation with TLR ligands, S6K1 deficiency causes a marked increase in TAK1 kinase activity that in turn induces a substantial enhancement of NF-κB-dependent gene expression, indicating that S6K1 is negatively involved in the TLR signaling pathway by the inhibition of TAK1 activity. Our findings contribute to understanding the molecular pathogenesis of the impaired immune responses seen in type 2 diabetes, where S6K1 plays a key role both in driving insulin resistance and modulating TLR signaling.</P>
Performance of prototype neutron detectors for Large Acceptance Multi-Purpose Spectrometer at RAON
Shim, Hyunha,Lee, Jong-Won,Hong, Byungsik,Ahn, Jung Keun,Bak, Gyeonghwan,Jo, Jamin,Kim, Minho,Kim, Young Jin,Kim, Young Jun,Lee, Hanseul,Lee, Hyo Sang,Lee, Kyong Sei,Mulilo, Benard,Moon, Dong Ho,Ryu, Elsevier 2019 Nuclear Instruments & Methods in Physics Research. Vol.927 No.-
<P><B>Abstract</B></P> <P>The performance of the prototype modules of neutron detectors for the Large Acceptance Multi-Purpose Spectrometer (LAMPS) was investigated, using cosmic muons and neutron beams at 65 and 392 MeV, provided by the Research Center for Nuclear Physics (RCNP). The timing and position resolutions were estimated using cosmic muons as 309 ps and 4.8 cm, respectively. The energy resolution depended on the incident energy of neutrons: 1.3% at 65 MeV and 3.1% at 392 MeV. The neutron-detection efficiency also showed weak energy dependence as it decreased from (9.0 ± 1.6)% at 65 MeV to (6.3 ± 1.0)% at 392 MeV.</P>
Conceptual Design of Soft X-ray Microscopy for Live Biological Samples
Kim, Kyong-Woo,Nam, Ki-Yong,Kwon, Young-Man,Shim, Seong-Taek,Kim, Kyu-Gyeom,Yoon, Kwon-Ha Optical Society of Korea 2003 Current Optics and Photonics Vol.7 No.4
This study describes the conceptual design of a soft x-ray microscope system based on a laserbased source for biomedical application with high resolution (${\leq}$50nm). The laboratory scale soft x-ray microscope consists of high power laser plasma x-ray source and grazing incidence mirrors with high reflectivity. The laser plasma source used for developing this system employs Q-switched Nd-YAG pulsed laser. The laser beam is focused on a tantalum (Ta) target. The Wolter type I mirror was used as condenser optics for sample illumination and as objective mirror for focusing on a detector. The fabrication of the Wolter type I mirror was direct internal cutting using ultraprecision DTM. A hydrated biological specimen was put between the two silicon wafers, the center of which was $Si_3N_4$ windows of 100㎚ thickness. The main issues in the future development work are to make a stable, reliable and reproducible x-ray microscope system.
Kim, Jaewook,Shim, In Kyong,Hwang, Dong Gyu,Lee, Yu Na,Kim, Myungji,Kim, Hyeonji,Kim, Seok-Won,Lee, Song,Kim, Song Cheol,Cho, Dong-Woo,Jang, Jinah The Royal Society of Chemistry 2019 Journal of materials chemistry. B, Materials for b Vol.7 No.10
<P>Type 1 diabetes mellitus (T1DM) is a form of diabetes that inhibits or halts insulin production in the pancreas. Although various therapeutic options are applied in clinical settings, not all patients are treatable with such methods due to the instability of the T1DM or the unawareness of hypoglycemia. Islet transplantation using a tissue engineering-based approach may mark a clinical significance, but finding ways to increase the function of islets in 3D constructs is a major challenge. In this study, we suggest pancreatic tissue-derived extracellular matrix as a potential candidate to recapitulate the native microenvironment in transplantable 3D pancreatic tissues. Notably, insulin secretion and the maturation of insulin-producing cells derived from human pluripotent stem cells were highly up-regulated when cultured in pdECM bioink. In addition, co-culture with human umbilical vein-derived endothelial cells decreased the central necrosis of islets under 3D culture conditions. Through the convergence of 3D cell printing technology, we validated the possibility of fabricating 3D constructs of a therapeutically applicable transplant size that can potentially be an allogeneic source of islets, such as patient-induced pluripotent stem cell-derived insulin-producing cells.</P>
Kim, Hyun Jong,Choi, Ji Hyun,Hwang, Jung-Hwan,Kim, Kyong-Shim,Noh, Jung-Ran,Choi, Dong-Hee,Moon, Sung Je,Kim, Hyun-Yong,Kim, Sang-Woo,Choi, Sangho,Eum, Sang Mi,Bach, Tran The,Rho, Jaerang,Lee, Ju Yong UNKNOWN 2018 INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE Vol.42 No.5
<P><I>Melicope ptelefolia</I> has been traditionally used to treat rheumatism and fever. The present study aimed to investigate the therapeutic effect of 3,5-di-C-<I>β</I>-<SUB><SMALL>D</SMALL></SUB>-glucopyranosyl phloroacetophenone (βGP), a main component of <I>M. ptelefolia</I>, on rheumatoid arthritis (RA). A model of collagen-induced arthritis (CIA) was established in mice using the RAW 264.7 murine macrophage cell line and mouse embryonic fibroblasts (MEFs). The clinical scores of arthritis, swelling, histopathological findings, and micro-computed tomography in CIA mouse paws were assessed. The levels of anti-type II collagen antibody and cytokines were determined in the plasma and cell culture supernatant, respectively. Protein and gene expression levels were analyzed by western blot and reverse transcription-quantitative polymerase chain reaction analyses. βGP significantly decreased the gross arthritic scores of CIA mice and joint swelling, and decreased articular inflammation, cartilage degradation and bone erosion. However, βGP did not exert any effect on anti-type II collagen immunoglobulin G plasma levels or inflammatory cytokine expression in macrophages. βGP significantly suppressed the expression of interleukin-6 and leukemia inhibitory factor and decreased the phosphorylation of signal transducer and activator of transcription 3, and expression of receptor activator of nuclear factor-κB ligand in tumor necrosis factor-α-stimulated MEFs and in CIA mouse paws. Osteoclast-related gene expression was significantly reduced in CIA mouse paws. Taken together, βGP suppressed the development of RA by regulating the activation of synovial fibroblasts.</P>
Jae Kyong Kim, Se Eun Kim, Chun-Sik Bae, Kyung Mi Shim, Seok Hwa Choi, Soon-Jeong Jeong, Seong Soo Kang 충북대학교 동물의학연구소 2013 Journal of Biomedical and Translational Research Vol.14 No.1
This study was conducted in order to examine the effects of alcohol-free cetylpyridinium chloride drinking water additive and oral gel on clinical parameters related to periodontal disease in beagle dogs. This study was conducted with healthy 15 beagle dogs. Following a professional teeth cleaning procedure, dogs were divided into three groups. Dogs in the control group received nothing, those in the drinking water additive (DWA) group received 800 ml water with 15 ml of alcohol-free cetylpyridinium chloride drinking water additive daily, and those in the Oral gel (OG) group were treated with oral gel containing alcohol-free cetylpyridinium chloride and 0.05% chlorhexidine gluconate daily. Clinical parameters, including plaque index (PI), calculus index (CI), and gingivitis index (GI) were evaluated at two and four weeks. Dogs in the DWA and OG groups had significantly less plaque than dogs in the control group at two and four weeks (P<0.01, P<0.05). And, at four weeks, CI was significantly lower in the OG group compared to the control group (P<0.05). On GI, similar scores were recorded for all groups during the experimental period. No significant difference was observed between the DWA group and the OG group. The effect of alcohol-free cetylpyridinium chloride drinking water additive was similar to the result for alcohol containing cetylpyridinium chloride mouthwash reported in a previous study. The effect in control of periodontal disease was better in the OG group because of additional chlorhexidine gluconate. However, use of drinking water additive will be more convenient for owners; thus, it will be more effective for achievement of long-term results.
Effects of mesenchymal stem cells treated with BMP-2 and VEGF on regeneration of large bone defects
Jae Kyong Kim, Se Eun Kim, Kyung Mi Shim, Chun-Sik Bae, Seok Hwa Choi, Seong Soo Kang 충북대학교 동물의학연구소 2014 Journal of Biomedical and Translational Research Vol.15 No.1
This study evaluated the possibility of clinical application using matrigel-based bioceramic/polymer scaffolds treated with bone morphogenetic protein, angiogenic factor, and mesenchymal stem cells (MSCs) for new bone formation. In the in vitro study, bone morphogenetic protein (BMP-2) and vascular endothelial growth factor (VEGF) containing matrigel, which is a basement membrane gel, was injected into HA/PCL scaffolds to estimate the release rates of growth factors. In the in vivo study, BMP-2, VEGF, and MSCs with matrigel-based scaffolds were implanted into rat femoral segmental defects, and new bone formation was evaluated at 4 and 8 weeks. In the results, the release rates of BMP-2 and VEGF explosively increased by day 5. For the in vivo study results, radiological evaluation revealed that the matrigel-based HA/PCL scaffolds with BMP-2 and VEGF grafted (M+B+V) and matrigel-based HA/PCL scaffolds with BMP-2, VEGF, and MSC grafted (MSC) groups showed increased bone volume and bone mineral density. Moreover, in the histological evaluation, large new bone formation was observed in the M+B+V group, and high cellularity in the scaffold was observed in the MSC group. In conclusion, grafted matrigel-based HA/PCL scaffolds with BMP-2, angiogenic factor, and MSCs increased new bone formation, and in clinical cases, it may be effective and useful to enhance healing of delayed fractures.