• Title/Summary/Keyword: TSG-6

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Tumor necrosis factor-inducible gene 6 interacts with CD44, which is involved in fate-change of hepatic stellate cells

  • Wang, Sihyung;Kim, Jieun;Lee, Chanbin;Jung, Youngmi
    • BMB Reports
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    • v.53 no.8
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    • pp.425-430
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    • 2020
  • Tumor necrosis factor-inducible gene 6 protein (TSG-6) is a cytokine secreted by mesenchymal stem cells (MSCs) and regulates MSC stemness. We previously reported that TSG-6 changes primary human hepatic stellate cells (pHSCs) into stem-like cells by activating yes-associated protein-1 (YAP-1). However, the molecular mechanism behind the reprogramming action of TSG-6 in pHSCs remains unknown. Cluster of differentiation 44 (CD44) is a transmembrane protein that has multiple functions depending on the ligand it is binding, and it is involved in various signaling pathways, including the Wnt/β-catenin pathway. Given that β-catenin influences stemness and acts downstream of CD44, we hypothesized that TSG-6 interacts with the CD44 receptor and stimulates β-catenin to activate YAP-1 during TSG-6-mediated transdifferentiation of HSCs. Immunoprecipitation assays showed the interaction of TSG-6 with CD44, and immunofluorescence staining analyses revealed the colocalization of TSG-6 and CD44 at the plasma membrane of TSG-6-treated pHSCs. In addition, TSG-6 treatment upregulated the inactive form of phosphorylated glycogen synthase kinase (GSK)-3β, which is a negative regulator of β-catenin, and promoted nuclear accumulation of active/nonphosphorylated β-catenin, eventually leading to the activation of YAP-1. However, CD44 suppression in pHSCs following CD44 siRNA treatment blocked the activation of β-catenin and YAP-1, which inhibited the transition of TSG-6-treated HSCs into stem-like cells. Therefore, these findings demonstrate that TSG-6 interacts with CD44 and activates β-catenin and YAP-1 during the conversion of TSG-6-treated pHSCs into stem-like cells, suggesting that this novel pathway is an effective therapeutic target for controlling liver disease.

2,3,5,4'-Tetrahydroxystilbene-2-O-β-D-Glucoside modulated human umbilical vein endothelial cells injury under oxidative stress

  • Guo, Yan;Fan, Wenxue;Cao, Shuyu;Xie, Yuefeng;Hong, Jiancong;Zhou, Huifen;Wan, Haitong;Jin, Bo
    • The Korean Journal of Physiology and Pharmacology
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    • v.24 no.6
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    • pp.473-479
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    • 2020
  • Endothelial cell injury is a major contributor to cardiovascular diseases. The 2,3,5,4'-Tetrahydroxystilbene-2-O-β-D-Glucoside (TSG) contributes to alleviate human umbilical vein endothelial cells (HUVECs) injury through mechanisms still know a little. This study aims to clarify the TSG effects on gene expression (mRNA and microRNA) related to oxidative stress and endoplasmic reticulum stress induced by H2O2 in HUVECs. We found that TSG significantly reduced the death rate of cells and increased intracellular superoxide dismutase activity. At qRT-PCR, experimental data showed that TSG significantly counteracted the expressions of miR-9-5p, miR-16, miR-21, miR-29b, miR-145-5p, and miR-204-5p. Besides, TSG prevented the expression of ATF6 and CHOP increasing. In contrast, TSG promoted the expression of E2F1. In conclusion, our results point to the obvious protective effect of TSG on HUVECs injury induced by H2O2, and the mechanism may through miR16/ATF6/ E2F1 signaling pathway.

Thermosalinograph Measurements in the Western Pacific Ocean in May and June, 2001 (2001년 5월과 6월 서태평양에서의 Thermosalinograph 관측)

  • Lee, Jae-Hak;Chung, Byoung-Chul;Hwang, Keun-Choon;Jeon, Dong-Chull;Hwang, Sang-Chul;Lee, Ha-Woong
    • Ocean and Polar Research
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    • v.24 no.3
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    • pp.207-213
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    • 2002
  • We have analyzed sea surface temperature and salinity data collected in the western Pacific Ocean by using an automated Thermosalinograph (TSG) installed on the RV Onnuri during May - June of 2001. The TSG data exhibit characteristics of water masses distributed in the near surface layer of the cruise area very well. Especially, they reveal the diurnal surface temperature cycle and the effect of rainfall on temperature and salinity in the equatorial region, showing the effectiveness of the use of TSG. Problems to be improved for the better TSG operation are the method of water sampling and calibration of TSG sensors. Installation of a pressure gauge in the TSG system and periodical sensor calibration are strongly recommended to ensure reliability of data.

Standardization Trends of 3GPP TSG RAN WG 2 (3GPP TSG RAN WG 2의 표준화 동향 분석)

  • Choi, J.H.;Song, P.J.
    • Electronics and Telecommunications Trends
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    • v.16 no.6 s.72
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    • pp.126-132
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    • 2001
  • WCDMA 비동기 방식의 IMT-2000 규격 정립을 위해, 3GPP의 여러 실무 그룹에서 Release ’99, Release ’4 및 Release ’5에 대한 표준화가 동시에 이루어지고 있다. 본 고에서는 UTRA 프로토콜의 계층 2와 3 표준화를 담당하고 있는 3GPP TSG RAN WG 2의 규격의 표준화 현황 및 새로이 규격에 반영될 기술들에 대해 살펴본다.

A study on the authentication mechanism of W-CDMA IMT-2000 system (W-CDMA 방식 IMT-2000 시스템에서의 인증에 관한 연구)

  • 김건우;정배은;장구영;류희수
    • Journal of the Korea Institute of Information Security & Cryptology
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    • v.11 no.6
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    • pp.53-65
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    • 2001
  • Authentication mechanism for W-CMDA IMT-2000 system is developed by 3GPP TSG SA WG3. We simulated the mechanism and algorithms. In this paper, we overview 3GPP authentication procedures and present results of our simulation. We validate the mechanism and parameters transmitted during authentication procedures and we also discuss parameters which are unclear in specification.

Changes in the components of salivary exosomes due to initial periodontal therapy

  • Arisa Yamaguchi;Yuto Tsuruya;Kazuma Igarashi;Zhenyu Jin;Mizuho Yamazaki-Takai;Hideki Takai;Yohei Nakayama;Yorimasa Ogata
    • Journal of Periodontal and Implant Science
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    • v.53 no.5
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    • pp.347-361
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    • 2023
  • Purpose: Exosomes are membrane vesicles that are present in body fluids and contain proteins, lipids, and microRNA (miRNA). Periodontal tissue examinations assess the degree of periodontal tissue destruction according to the probing depth (PD), clinical attachment loss (CAL), bleeding on probing, and X-ray examinations. However, the accurate evaluation of the prognosis of periodontitis is limited. In this study, we collected saliva from patients before and after initial periodontal therapy (IPT) and compared changes in the clinical parameters of periodontitis with changes in the components of salivary exosomes. Methods: Saliva was collected from patients with stage III and IV periodontitis at the first visit and post-IPT. Exosomes were purified from the saliva, and total protein and RNA were extracted. Changes in expression levels of C6, CD81, TSG101, HSP70, and 6 kinds of miRNA were analyzed by western blots and real-time polymerase chain reaction. Results: Patients with increased C6 expression after IPT had significantly higher levels of periodontal inflamed surface area (PISA), miR-142, and miR-144 before and after IPT than patients with decreased C6 expression after IPT. Patients with decreased and unchanged CD81 expression after IPT showed significantly higher PD, CAL, and PISA before IPT than after IPT. Patients with decreased and unchanged TSG101 expression after IPT had significantly higher PD before IPT than after IPT. Patients with increased HSP70 expression after IPT had significantly higher PD and PISA before and after IPT than patients with unchanged HSP70 after IPT. The expression levels of miR-142, miR-144, miR-200b, and miR-223 changed with changes in the levels of C6, CD81, TSG101, and HSP70 in the salivary exosomes of periodontitis patients before and after IPT. Conclusions: The expression levels of proteins and miRNAs in salivary exosomes significantly changed after IPT in periodontitis patients, suggesting that the components of exosomes could serve as biomarkers for periodontitis.

3GPP의 IMT-2000 인증 체계에서의 취약성 분석

  • 이덕규;이임영;안정철;김춘수
    • Review of KIISC
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    • v.11 no.6
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    • pp.63-73
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    • 2001
  • 3세대 방식인 IMT-2000 (International Mobile Telecommunication-2000)시스템은 GSM이나 IS-95 CDMA 시스템과 같은 2세대 이동통신 시스템과 비교하여 고속의 멀티미디어 서비스 제공 및 글로벌 로밍을 특징으로 한다. W-CDMA 방식 IMT-2000에 대한 인증 메커니즘은 3GPP TSG SA WG3에 의해서 개발되었다. 본 논문에서는 3GPP에서의 AKA(Authentication & Key Agreement)를 분석하고 이를 통해 안전성 분석 및 취약성을 분석한다. 본 논문에서 제기하는 안전성 분석 및 취약성 분석은 앞으로의 더 좋은 서비스를 제공할 것이다.