• 제목/요약/키워드: TGF

검색결과 936건 처리시간 0.03초

TGF-β1 upregulates the expression of hyaluronan synthase 2 and hyaluronan synthesis in culture models of equine articular chondrocytes

  • Ongchai, Siriwan;Somnoo, Oraphan;Kongdang, Patiwat;Peansukmanee, Siriporn;Tangyuenyong, Siriwan
    • Journal of Veterinary Science
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    • 제19권6호
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    • pp.735-743
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    • 2018
  • We investigated the effect of transforming growth factor beta 1 ($TGF-{\beta}1$) on equine hyaluronan synthase 2 (HAS2) gene expression and hyaluronan (HA) synthesis in culture models of articular chondrocytes. Equine chondrocytes were treated with $TGF-{\beta}1$ at different concentrations and times in monolayer cultures. In three-dimensional cultures, chondrocyte-seeded gelatin scaffolds were cultured in chondrogenic media containing 10 ng/mL of $TGF-{\beta}1$. The amounts of HA in conditioned media and in scaffolds were determined by enzyme-linked immunosorbent assays. HAS2 mRNA expression was analyzed by semi-quantitative reverse transcription polymerase chain reaction. The uronic acid content and DNA content of the scaffolds were measured by using colorimetric and Hoechst 33258 assays, respectively. Cell proliferation was evaluated by using the alamarBlue assay. Scanning electron microscopy (SEM), histology, and immunohistochemistry were used for microscopic analysis of the samples. The upregulation of HAS2 mRNA levels by $TGF-{\beta}1$ stimulation was dose and time dependent. $TGF-{\beta}1$ was shown to enhance HA and uronic acid content in the scaffolds. Cell proliferation and DNA content were significantly lower in $TGF-{\beta}1$ treatments. SEM and histological results revealed the formation of a cartilaginous-like extracellular matrix in the $TGF-{\beta}1$-treated scaffolds. Together, our results suggest that $TGF-{\beta}1$ has a stimulatory effect on equine chondrocytes, enhancing HA synthesis and promoting cartilage matrix generation.

Transforming growth factor-beta and liver injury in an arginine vasopressin-induced pregnant rat model

  • Govender, Nalini;Ramdin, Sapna;Reddy, Rebecca;Naicker, Thajasvarie
    • Clinical and Experimental Reproductive Medicine
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    • 제48권2호
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    • pp.124-131
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    • 2021
  • Objective: Approximately 30% of preeclamptic pregnancies exhibit abnormal liver function tests. We assessed liver injury-associated enzyme levels and circulating transforming growth factor beta (TGF-β) levels in an arginine vasopressin (AVP)-induced pregnant Sprague-Dawley rat model. Methods: Pregnant and non-pregnant Sprague-Dawley rats (n=24) received AVP (150 ng/hr) subcutaneously via mini-osmotic pumps for 18 days. Blood pressure was measured, urine samples were collected, and all animals were euthanized via isoflurane. Blood was collected to measure circulating levels of TGF-β1-3 isomers and liver injury enzymes in pregnant AVP (PAVP), pregnant saline (PS), non-pregnant AVP (NAVP), and non-pregnant saline (NS) rats. Results: The PAVP group showed significantly higher systolic and diastolic blood pressure than both saline-treated groups. The weight per pup was significantly lower in the AVP-treated group than in the saline group (p<0.05). Circulating TGF-β1-3 isomer levels were significantly higher in the PAVP rats than in the NS rats. However, similar TGF-β1 and TGF-β3 levels were noted in the PS and PAVP rats, while TGF-β2 levels were significantly higher in the PAVP rats. Circulating liver-type arginase-1 and 5'-nucleotidase levels were higher in the PAVP rats than in the saline group. Conclusion: This is the first study to demonstrate higher levels of TGF-β2, arginase, and 5'-nucleotidase activity in PAVP than in PS rats. AVP may cause vasoconstriction and increase peripheral resistance and blood pressure, thereby elevating TGF-β and inducing the preeclampsia-associated inflammatory response. Future studies should explore the mechanisms through which AVP dysregulates liver injury enzymes and TGF-β in pregnant rats.

마황(麻黃)과 Silymarin의 병용이 TGF-β/Smad 경로 억제를 통한 간섬유화 억제효능 (Combination of EHE and Silymarin ameliorates liver fibrosis by inhibiting TGF-β/Smad pathway in LX-2 cells)

  • 박상미;진효정;김예림;박숙자;김상찬
    • 대한본초학회지
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    • 제39권4호
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    • pp.19-28
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    • 2024
  • Objectives : Ephedrae Herba has been used in the East Asian traditional medicine, for treatment of asthma, cold and influenza. Silymarin is an effective antioxidant and its anti-fibrogenic, anti-inflammatory, and hepatoprotective properties have been reported. This study was performed to explore an anti-fibrogenic potential of Ephedrae Herba extract (EHE) + silymarin on immortalized human hepatic stellate cell line, LX-2 cells. Methods : We studied the anti-fibrogenic effects of EHE + silymarin on transforming growth factor β1 (TGF-β1) signaling pathway in LX-2 cells. Cell viability was measured using the MTT assay. mRNA levels were detected by real-time PCR. TGF-β1 signaling-related proteins expression were detected by Western blot. Results : Silymarin 30 ㎍/mL and EHE 100 ㎍/mL showed cytotoxicity on LX-2 cells. Therefore, the concentrations of silymarin and EHE were studied at 10 ㎍/mL, respectively. Silymarin significantly reduced PAI-1 protein expression, Smad binding element (SBE) luciferase activity, and mRNA (PAI-1, MMP2 and 9) expression compared to TGF-β1. EHE significantly reduced SBE luciferase activity and mRNA (PAI-1, MMP2 and 9) expression compared to TGF-β1. More importantly, EHE + silymarin significantly reduced all parameters compared to TGF-β1, and also significantly reduced compared to EHE alone and silymarin alone. Conclusion : The results indicate that EHE + silymarin has anti-fibrogenic effect in LX-2 cells induced by TGF-β1. Additionally, EHE + silymarin shows more effective anti-fibrogenic effect than EHE alone and silymarin alone.

Regulation of Tumor Immune Surveillance and Tumor Immune Subversion by TGF-$\beta$

  • Park, Hae-Young;Wakefield, Lalage M;Mamura, Mizuko
    • IMMUNE NETWORK
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    • 제9권4호
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    • pp.122-126
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    • 2009
  • Transforming growth factor-$\beta$ (TGF-$\beta$) is a highly pleiotropic cytokine playing pivotal roles in immune regulation. TGF-$\beta$ facilitates tumor cell survival and metastasis by targeting multiple cellular components. Focusing on its immunosuppressive functions, TGF-$\beta$ antagonists have been employed for cancer treatment to enhance tumor immunity. TGF-$\beta$ antagonists exert anti-tumor effects through #1 activating effector cells such as NK cells and cytotoxic $CD8^+$ Tcells (CTLs), #2 inhibiting regulatory/suppressor cell populations, #3 making tumor cells visible to immune cells, #4 inhibiting the production of tumor growth factors. This review focuses on the effect of TGF-$\beta$ on T cells, which are differentiated into effector T cells or newly identified tumor-supporting T cells.

Histopathologic Study and Expression of $TGF-{\beta}1$ of Choanal Polyp

  • Ahn, Byung-Hoon
    • The Korean Journal of Physiology and Pharmacology
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    • 제5권4호
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    • pp.353-357
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    • 2001
  • The pathogenesis of the nasal polyp is multifactorial and choanal polyps can be defined by its origin of genesis: antrochoanal (maxillochoanal), ethmochoanal and sphenochoanal polyp. Transforming growth $factor-{\beta}\;(TGF-{\beta})$ has various biologic activities, including the regulation of epithelial proliferation, the promotion of extracellular matrix formation and the induction of angiogenesis, hence closely related to pathogenesis of nasal polyp. Twenty cases of choanal polyps (13 antrochoanal, 4 ethmochoanal and 3 sphenochoanal polyps) were included in this study. Each polyp was subdivided into its origin, pedicle and choanal part. Hematoxylin and eosin stain for routine histopathology and immunohistochemistry were employed to detect expression of $TGF-{\beta}1.$ According to polyp type, edematous type is common at origin part and fibrous type at choanal part, and showed no difference at pedicle part in frequency. In ethmochoanal and sphenochoanal polyps, glandulocystic and edematous type is more common than fibrous type. $TGF-{\beta}1$ was expressed in epithelial cells, endothelial cells, eosinophils and lymphocytes. There was no different expression of $TGF-{\beta}1$ in each kind of choanal polyps and separate parts in each polyp. But histologic finding of choanal polyp is different between origin, pedicle and choanal part. Also infiltration of inflammatory cells including eosinophils has no difference between origin site. The expression of $TGF-{\beta}1$ was observed at all the choanal polyps and no difference between origin site and each portions was noted.

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돼지 난소의 황체세포의 체외배양시 TGF-${\beta}$1의 분비

  • 최재혁;김봉기;정학재;박진기;우제현;양병철;장유민;박수봉;성환후
    • 한국동물번식학회:학술대회논문집
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    • 한국동물번식학회 2003년도 학술발표대회 발표논문초록집
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    • pp.89-89
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    • 2003
  • 본 연구는 난소의 황체를 체외배양시 TGF-$\beta$1의 황체내 발현을 조사하기 위해 수행되었다. 돼지 황체는 축산기술연구소에서 사육중인 돼지(체중 145$\pm$kg) 12두로부터 발정을 유도시켜 배란 후 약 48시간째 도축하여 난소를 회수하였다. 회수된 난소로부터 황체를 분리하여 세절한 후 0.25% collagenase용액(0.025mg DNase, 50mM EDTA, 50mM Dithio-threitol)으로 37$^{\circ}C$의 진탕 수조에서 30분간 배양하여 황체세포를 분리 회수하였다. 회수된 황체세포는 D-MEM용액(GIBCO, 10% FCS와 antibiotics 첨가)으로 2회 세척하여 1$\times$$10^{6}$live cell/$m\ell$이 되도록 희석하여 24 well culture plate(Corning, New Tork 14831)에 분주하여 $CO_2$ 배양기($CO_2$: 5%)에서 24시간 간격으로 2회 배양액을 교환해 48시간 동안 배양하였다. 배양된 황체 세포는 immunocytochemistry 방법으로 TGF-$\beta$1의 발현을 관찰함과 동시에 황체조직도 같은 방법을 사용하여 TGF-$\beta$1 의 발현 유ㆍ무을 관찰하였다. 그 결과 황체세포 그리고 황체 조직 뚜렷한 TGF$\beta$1의 발현을 확인할 수 있었다. 이 결과로서 TGF$\beta$1은 황체기능을 유지하는데 하나의 인자로서 작용하며 다른 인자들과의 상호작용을 시사하고 있다.

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The Signaling Mechanism of TGF-β1 Induced Bovine Mammary Epithelial Cell Apoptosis

  • Di, He-Shuang;Wang, Li-Gang;Wang, Gen-Lin;Zhou, Lei;Yang, Yuan-Yuan
    • Asian-Australasian Journal of Animal Sciences
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    • 제25권3호
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    • pp.304-310
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    • 2012
  • The present study showed that Transforming growth factor beta 1 (TGF-${\beta}_1$) can induce apoptosis of bovine mammary epithelial cells. This apoptosis was also observed with phosphorylation of Smad2/3 within 0.5-2 h. Afterwards the signal transferred into the nucleus. Moreover, intracellular free $Ca^{2+}$ concentration was significantly elevated as well as Caspase-3 activated and DNA lysised, thereby inducing the programmed cell death. This signaling pathway of TGF-${\beta}_1$ was blocked by SB-431542 ($10^{-2}{\mu}M$) via inhibiting ALK-5 kinase activity, which thus reversed the anti-proliferation and apoptosis effect of TGF-${\beta}_1$ in mammary epithelial cells. These results indicated that TGF-${\beta}_1$ induced apoptosis of bovine mammary epithelial cells through the ALK-5-Smad2/3 pathway, which plays an important role in inhibiting survival of mammary epithelial cells. Moreover, intracellular $Ca^{2+}$ also played a critical role in TGF-${\beta}_1$-induced cell apoptosis.

Role of the transforming growth factor (TGF)-β1 and TGF-β1 signaling pathway on the pathophysiology of respiratory pneumococcal infections

  • Andrade, Maria Jose;Lim, Jae Hyang
    • Journal of Yeungnam Medical Science
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    • 제34권2호
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    • pp.149-160
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    • 2017
  • Streptococcus pneumoniae, pneumococcus, is the most common cause of community-acquired pneumonia (CAP). CAP is an important infectious disease with high morbidity and mortality, and it is still one of the leading causes of death worldwide. Many genetic factors of the host and various environmental factors surrounding it have been studied as important determinants of the pathophysiology and outcomes of pneumococcal infections. Various cytokines, including transforming growth factor $(TGF)-{\beta}1$, are involved in different stages of the progression of pneumococcal infection. $TGF-{\beta}1$ is a cytokine that regulates a wide range of cellular and physiological functions, including immune and inflammatory responses. This cytokine has long been known as an anti-inflammatory cytokine that is critical to preventing the progression of an acute infection to a chronic condition. On the other hand, recent studies have unveiled the diverse roles of $TGF-{\beta}1$ on different stages of pneumococcal infections other than mitigating inflammation. This review summarizes the recent findings of the role of $TGF-{\beta}1$ on the pathophysiology of pneumococcal infections, which is fundamental to developing novel therapeutic strategies for such infections in immune-compromised patients.

TGF-$\beta$1와 IGF-I이 소 난포란의 체외성숙 및 체외수정란의 배양에 미치는 영향 (Effect of TGF-$\beta$1 and IGF-I on Bovine In Vitro Maturation and Embryo Culture)

  • 서태광
    • 한국가축번식학회지
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    • 제20권2호
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    • pp.111-117
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    • 1996
  • 본 연구는 혈청첨가 또는 무첨가에 따른 소 난포란의 체외성숙에 있어서 참가된 TGF-$\beta$1과 IGF-I이 그후의 수정 및 발생에 미치는 영향과, 이들 growth factor의 농도에 따른 8세포기 소 체외수정란의 발달에 미치는 영향을 조사하고자 실시하였다. 도축장에서 얻어진 난소로부터 채취된 난포란을 20% FBS가 첨가 또는 첨가되지 않은 TCM-199에 TGF-$\beta$1, IGF-I 또는 TGF-$\beta$1+IGF-I을 각각 10ng/ml 첨가하여 38.5$^{\circ}C$에서 24시간 배양하여 체외성숙을 유기하였다. 성숙된 난자를 1$\times$106/ml 정자농도로 수정후 24시간에 glucoserk 첨가되지 않은 CZB 배양액으로 옮겨 48시간 배양한 다음, TCM-199+20%FBS에서 96시간 추가배양하였다. 본 연구에서 혈청이 첨가된 난포란의 체외성숙배양액에 첨가된 growth factor들은 수정후의 배분할 및 배발생에 영향을 미치지 않았다. 혈청이 첨가되지 않은 경우에서는 TGF-$\beta$1의 첨가는 배분할 및 배발생율을 향상시켰다(P<0.05). 한편 TCM-199+20%FBS에 5, 10ng/ml의 TGF-$\beta$1 및 5, 10, 50, 100ng/ml의 IGF-I을 각각 첨가후 8세포기 체외수정란을 배양한 결과, 10ng/ml TGF-$\beta$1의 첨가는 배반포기로의 발생율을 향상시켰다(P<0.05). 결론적으로, 혈청이 포함되지 않은 소 난포란의 체외성숙 배양액, 또는 수정란의 체외배양액에 10ng/ml TGF-1의 첨가는 배반포기로의 발생율을 향상시킨다.

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자연기흉환자의 폐기포에서 TGF-${\beta}1$ 단백질 발현에 대한 연구 (TGF-${\beta}1$ Protein Expression in Bullae of Patients with Spontaneous Pneumothorax)

  • 김광호;조정수;김영삼;윤용한;김정택;백완기;김루시아;송순욱
    • Journal of Chest Surgery
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    • 제39권11호
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    • pp.805-809
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    • 2006
  • 배경: Transforming growth factor-beta 1 receptor II(TGF-${\beta}1RII$) 단백질의 과발현이 폐기포 조직의 형성에 관여할 수 있다는 연구 결과를 본 연구팀은 발표한 바 있다. 이와 관련하여 폐기포벽에서 발견되는 섬유화에 관계될 것으로 생각되는 Transforming growth factor-beta 1(TGF-${\beta}1$) ligand의 발현의 변화를 보기 위하여 자연기흉 환자에서 폐기포 절제슬로 획득한 폐 기포조직을 면역조직화학적 염색법으로 염색하여 관찰하려 하였다. 대상 및 방법: 36명의 자연기흉의 환자에서 비디오흉강경 폐기포절제술 시 획득된 폐기포조직을 획득하였다. 36명 환자 중 남자가 34명, 여자가 2명이었고 연령은 14세에서 38세였다. 획득된 폐기포조직을 면역조직화학적 염색방법으로 염색하였다. 결과: 36명 중 19예에서 TGF-${\beta}1$ 양성이었고 24예에서는 transforming growth factor-beta 1 receptor II(TGF-${\beta}1RII$)가 양성이었다. 19예의 TGF-${\beta}1$ 양성 예 중 15예에서 TGF-${\beta}1RII$에도 양성으로 관찰되었다. 이 같은 양성 변화는 폐기포조직과 정상 폐 조직과의 경계선에서 가장 강하게 관찰되었다. 결론: TGF-${\beta}1$의 과발현은 TGF-${\beta}1RII$ 발현의 변이 여부와 마찬가지로 폐기포벽의 섬유화를 초래하여 폐기포 형성에 영향을 미치는 것으로 생각되며 확실한 규명을 위하여 분자생물학적 및 기타 추가적인 연구가 더 필요할 것으로 생각된다.