• 제목/요약/키워드: Th2 cell

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Supercapacitor용 $V_2O_5$-AC Composite의 충방전 특성 (Charge/discharge Properties of $V_2O_5$-AC Composite for Supercapacitor)

  • 김명산;김종욱;구할본
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 1999년도 추계학술대회 논문집
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    • pp.366-369
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    • 1999
  • The purpose of this study is to research and develop V2Os-AC(activated carbon) composite electrode for supercapacitor. Supaercapacitor cell of V2Os-AC composite electrode with 25P70FLiCIO$_{4}$/PC$_{10}$/EC$_{10}$ polymer electrolyte bring out good capacitor Performance below 3V. The discharge capacitance of V2Os-AC(30:70) composite with 70wt.% AC in 1st and 200th cycles was 9.6 and 8.2 F/g at current density of 1m7/cm2. The capacitance of V$_2$O$_{5}$-AC composite with 70wt.% AC capacitor was larger than that of others. The coulombic efficiency of supercapacitor at discharge process of 1 and 200 cycles were 96 and 100%, respectively. V$_2$O$_{5}$-AC composite supercapacitor with 70wt.% AC content showed good capacitance and stability with cycling.ing.ing.

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월국환합보중익기탕(越鞠丸合補中益氣湯)이 전기자극(電氣刺戟)스트레스를 받은 mouse의 면역기능(免疫機能)에 미치는 영향(影響) (Effects of Walgookwhanhab-Bojoongikgitang administration on immune-function in Balb/c mice stressed by electric footshock)

  • 권태식;이숙경;구병수
    • 동국한의학연구소논문집
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    • 제9권
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    • pp.51-71
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    • 2000
  • 본 실험은 월국환합보중익기탕(越鞠丸合補中益氣湯)의 항스트레스효과를 조사하기 위하여 시행되었다. 월국환합보중익기탕(越鞠丸合補中益氣湯)이 전기자극으로 스트레스 상황을 유발시킨 mouse에게 끼친 B 임파구 면역계 변화를 mouse 혈청의 면양적혈구(綿羊赤血球)에 대한 적혈구 응집소가와 비장세포에서 B 세포 및 T 세포가 차지하는 백분율의 변화를 통하여 측정하였으며 이를 대조군과 비교 분석하였다. 혈청 항체가의 측정에서 스트레스 자극하에서 월국환합보중익기탕(越鞠丸合補中益氣湯)을 투여받은 그룹에서 약제를 투여받지 않은 그룹에 비하여 유의성 있는 차이를 보여(p<0.01) 면역 기능을 정상군의 수준으로 유지하는 결과를 얻었다. T 세포와 B 세포의 백분율의 측정에서도 스트레스 자극하에서 월국환합보중익기탕(越鞠丸合補中益氣湯)을 투여 받은 그룹에서 약제를 투여 받지 않은 그룹에 비하여 유의성 있는 차이를 보여(p<0.01) 면역 기능을 정상군의 수준으로 유지하는 결과를 얻었다. 실험결과들로 보아 월국환합보중익기탕(越鞠丸合補中益氣湯)이 체액성 면역 반응과 비장 내 면역 세포의 백분율을 정상의 수준으로 유지하는 효과를 보여 면역 기능의 이상에 응용할 수 있는 가능성을 제시한다고 사료된다.

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신경성장촉진 인자가 인간 배아줄기세포 유래 도파민 분비 신경세포형성에 미치는 영향 (Effects of Neurotrophic Factors on the Generation of Functional Dopamine Secretory Neurons Derived from in vitro Differentiated Human Embryonic Stem Cells)

  • 이금실;김은영;신현아;조황윤;왕규창;김용식;이훈택;정길생;이원돈;박세필;임진호
    • Clinical and Experimental Reproductive Medicine
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    • 제31권1호
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    • pp.19-27
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    • 2004
  • Objective: This study was to examine the in vitro neural cell differentiation patterns of human embryonic stem (hES) cells following treatment of various neurotrophic factors [basic fibroblast growth factor (bFGF), retinoic acid (RA), brain derived neurotrophic factor (BDNF) and transforming growth factor (TGF)-$\alpha$], particulary in dopaminergic neuron formation. Methods: The hES cells were induced to differentiate by bFGF and RA. Group I) In bFGF induction method, embryoid bodies (EBs, for 4 days) derived from hES were plated onto gelatin dish, selected for 8 days in ITSFn medium and expanded at the presence of bFGF (10 ng/ml) for another 6 days followed by a final differentiation in N2 medium for 7, 14 and 21 days. Group II) For RA induction, EBs were exposed of RA ($10^{-6}M$) for 4 days and allowed to differentiate in N2 medium for 7, 14 and 21 days. Group III) To examine the effects of additional neurotrophic factors, bFGF or RA induced cells were exposed to either BDNF (10 ng/ml) or TGF-$\alpha$ (10 ng/ml) during the 21 days of final differentiation. Neuron differentiation and dopamine secretion were examined by indirect immunocytochemistry and HPLC, respectively. Results: The bFGF or RA treated hES cells were resulted in similar neural cell differentiation patterns at the terminal differentiation stage, specifically, 75% neurons and 11% glial cells. Additionally, treatment of hES cells with BDNF or TGF-$\alpha$ during the terminal differentiation stage led to significantly increased tyrosine hydroxylase (TH) expression of a dopaminergic neuron marker, compared to control (p<0.05). In contrast, no effect was observed on the rate of mature neuron (NF-200) or glutamic acid decarboxylase-positive neurons. Immunocytochemistry and HPLC analyses revealed the higher levels of TH expression (20.3%) and dopamine secretion (265.5 $\pm$ 62.8 pmol/mg) in bFGF and TGF-sequentially treated hES cells than those in $\alpha$ RA or BDNF treated hES cells. Conclusion: These results indicate that the generation of dopamine secretory neurons from in vitro differentiated hES cells can be improved by TGF-$\alpha$ addition in the bFGF induction protocol.

LPB용 MCMB 부극 도전재로 VGCF를 첨가한 부극의 특성 연구 (Characteristics of MCMB Anode with VGCF As a Conducting Agent for LPB)

  • 진봉수;도칠훈;문성인;윤문수;정재국;남효덕;박희구
    • 전기화학회지
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    • 제7권3호
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    • pp.143-147
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    • 2004
  • Vapor grown carbon fiber(VGCF)가 각기 달리 첨가된 부극으로 제조된 LPB의 특성을 조사하였다. MCMB를 활물질로, VGCF를 도전재로 사용하였을 경우, 전지의 내부저항과 1차 Ah효율은 VGCF첨가량이 많아질수록 감소하였고 방전 용량과 이용률은 증가하였다. $6wt\%$의 VGCF가 첨가된 부극으로 제조된 전지가 최저 임피던스를 나타내었고, $8wt\%$의 VGCF첨가한 경우는 VGCF를 첨가하지 않은 것과 유사한 임피던스를 나타내었다. $6wt\%$의 VGCF가 첨가된 부극으로 제조된 전지가 최고의 전지 특성을 나타내었다. 이 전지의 내부저항은 실온에서 $0.918\Omega$이였고, 2C에서의 고율 방전 시의 용량은 $93\%$였다. 율 특성과 수명 특성은 $4wt\%$$6wt\%$운의 VGCF가 첨가된 부극으로 제조된 전지가 타 전지에 비해 우수하였고 두 경우는 매우 유사한 결과를 나타내었다. $6wt\%$의 VGCF가 첨가된 부극으로 제조된 전지의 경우, 방전 용량은 충방전 사이클링을 진행함에 따라 서서히 감소하여 100회에서 178mAh/g의 비용량을 나타내었으며 이후에는 완만한 감소경향을 나타내었다. $6wt\%$의 VGCF첨가의 경우 이용률은 100회에서 $90\%$ 이상으로 $4wt\%$의 VGCF가 첨가된 부극으로 제조된 전지 보다 우수하였다.

개에서 땀샘 암종, 유선종양 및 방광 이행상피암종의 동시 발생 (Concurrence of Apocrine Carcinoma, Mammary Gland Tumors and Bladder Transitional Cell Carcinoma in a Dog)

  • 정연철;우계형;윤영민;김재훈
    • 한국임상수의학회지
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    • 제33권1호
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    • pp.74-79
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    • 2016
  • A 7-year-old female Pointer dog with multiple masses in the axilla, mammary gland, and bladder was submitted to the Pathology Department of the College of Veterinary Medicine in the Jeju National University. Grossly, mass between right axilla and 1st mammary gland, $15{\times}10cm$ in size, was well delineated and firm, slightly soft center, oval shape. And masses in right 1st, 3rd and 5th mammary gland were well delineated and sulphur yellow in color on the cut-surface. Numerous round to oval shaped masses, 0.3 to 2 cm in diameter were existed in the lung. Urinary bladder mucosa had rough and thick and round to oval papillary masses, 0.1 to 2 cm in diameter, on surface. Microscopically, masses in right axilla, 1st mammary gland, lung and axillary lymph node were composed of poorly differentiated tubules originated from apocrine gland. Lining neoplastic epithelium showed high mitotic figures, typical apical secretory blebs, and PAS-positive diastase-resistant cytoplasmic granules. Masses in 3rd and 5th mammary gland were confirmed as mammary complex adenoma and simple adenoma respectively. The masses in the urinary bladder were covered with stratified transitional epithelium with marked cellular atypia and high mitotic figures. Some neoplastic cells showed focal invasion into substantia propria of bladder. Immunohistochemaically, neoplastic transitional epithelium demonstrated positive reactions for cytokeratin 7, AE1/AE3, and MNF116. Based on the gross, histopathologic and immunohistochemical characteristics, this dog was diagnosed as apocrine carcinoma, mammary gland tumor including simple adenoma and complex adenoma and bladder transitional cell carcinoma. And distant metastases of apocrine carcinoma in right axilla were observed in axillary lymph node and lungs. This is the first report for concurrent occurrence of apocrine carcinoma, mammary gland tumor, and transitional cell carcinoma in a same dog.

17β-Estradiol이 progesterone target cell 분포에 미치는 영향에 대한 면역조직화학적 연구 I. 방사선자기법을 이용한 target cell의 분포에 대하여 (Immunohistochemical study on distribution of progesterone target cells by 17β-Estradiol I. Distribution of progesterone target cells by autoradiography)

  • 곽수동;고필옥;김종섭
    • 대한수의학회지
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    • 제36권1호
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    • pp.93-99
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    • 1996
  • This study was designed to investigate the effect of estrogen(Est) on the progestcrone(Prog) target cells by autoradiography. The spayed 16 mice(ICR, approximately 18~25g) were randomly alloted into 3 groups. $^3H$-Prog-treated group were injected with $40{\mu}Ci$ of $^3H$-Prog/mouse/day for 1 day, Est + $^3H$-Prog-treated group with $20{\mu}Ci$ of $17{\beta}$-Est/mouse/day for 3 days and then with $40{\mu}Ci$ of $^3H$-Prog/mouse at 4th day, and Est+$^3H$-thymidine(TdR)-treated group with $20{\mu}g$ of $17{\beta}$-Est/mouse/day for 3 days and then $80{\mu}Ci$ of $^3H$-TdR/mouse at 4th days. 1. Mice uteri of both Est+$^3H$-Prog-treated group and Est+$^3H$-TdR-treated group were hypemophied in gross finding and the endometrium and myometrium were thickened in microscopic findings. These findings were confirmed that Est enlarged the uteri of mice. 2. Cryo-preparations of mice organs were processed for autoradiography using Kodak NTB-2 emulsion following Kodak D-19 developer and hematoxylin counterstain. In each group, the number values of silver grain distribution appeared to be higher in the $^3H$-Prog-treated group than in the Est+$^3H$-Prog-treated group. It was considered that Est and Prog inhibit each other in action. 3. In both $^3H$-Prog-treated group and Est+$^3H$-Prog-treated group, the uteri have highest distribution rates of silver grains than in other organs, and the cerebral neurons, hepatocytes, bronchiolar epithelial cells and splenic reticular cells also contained some silver grains. 4. The orders of the cell types with more number of silver grains in the uteri were stromal cells, glandular epithelial cells, luminal surface cells and muscular cells and also were as above orders in distribution of proliferating cell type by $^3H$-TdR.

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Effects of in vitro vitamin D treatment on function of T cells and autophagy mechanisms in high-fat diet-induced obese mice

  • Kang, Min Su;Park, Chan Yoon;Lee, Ga Young;Cho, Da Hye;Kim, So Jeong;Han, Sung Nim
    • Nutrition Research and Practice
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    • 제15권6호
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    • pp.673-685
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    • 2021
  • BACKGROUND/OBJECTIVES: Obesity is associated with the impaired regulation of T cells characterized by increased numbers of Th1 and Th17 cells and the dysregulation of vitamin D metabolism. Both obesity and vitamin D have been reported to affect autophagy; however, a limited number of studies have investigated the effects of vitamin D on T cell autophagy in obese mice. Therefore, we aimed to determine whether in vitro treatment with vitamin D affects the proliferation, function, and autophagy of T cells from obese and control mice. MATERIALS/METHODS: Five-week-old male C57BL/6 mice were fed control or high-fat diets (10% or 45% kcal fat: CON or HFDs, respectively) for 12 weeks. Purified T cells were stimulated with anti-CD3 and anti-CD28 monoclonal antibodies and cultured with either 10 nM 1,25(OH)2D3 or 0.1% ethanol (vehicle control). The proliferative response; expression of CD25, Foxp3, RORγt, and autophagy-related proteins (LC3A/B, SQSTM1/P62, BECLIN-1, ATG12); and the production of interferon (IFN)-γ, interleukin (IL)-4, IL-17A, and IL-10 by T cells were measured. RESULTS: Compared with the CON group, T cell proliferation tended to be lower, and the production of IFN-γ was higher in the HFD group. IL-17A production was reduced by 1,25(OH)2D3 treatment in both groups. The LC3 II/I ratio was higher in the HFD group than the CON group, but P62 did not differ. We observed no effect of vitamin D treatment on T cell autophagy. CONCLUSIONS: Our findings suggest that diet-induced obesity may impair the function and inhibit autophagy of T cells, possibly leading to the dysregulation of T cell homeostasis, which may be behind the aggravation of inflammation commonly observed in obesity.

Human Organic Anion Transporting Polypeptide 1B3 Applied as an MRI-Based Reporter Gene

  • Song-Ee Baek;Asad Ul-Haq;Dae Hee Kim;Hyoung Wook Choi;Myeong-Jin Kim;Hye Jin Choi;Honsoul Kim
    • Korean Journal of Radiology
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    • 제21권6호
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    • pp.726-735
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    • 2020
  • Objective: Recent innovations in biology are boosting gene and cell therapy, but monitoring the response to these treatments is difficult. The purpose of this study was to find an MRI-reporter gene that can be used to monitor gene or cell therapy and that can be delivered without a viral vector, as viral vector delivery methods can result in long-term complications. Materials and Methods: CMV promoter-human organic anion transporting polypeptide 1B3 (CMV-hOATP1B3) cDNA or CMV-blank DNA (control) was transfected into HEK293 cells using Lipofectamine. OATP1B3 expression was confirmed by western blotting and confocal microscopy. In vitro cell phantoms were made using transfected HEK293 cells cultured in various concentrations of gadoxetic acid for 24 hours, and images of the phantoms were made with a 9.4T micro-MRI. In vivo xenograft tumors were made by implanting HEK293 cells transfected with CMV-hOATP1B3 (n = 4) or CMV-blank (n = 4) in 8-week-old male nude mice, and MRI was performed before and after intravenous injection of gadoxetic acid (1.2 µL/g). Results: Western blot and confocal microscopy after immunofluorescence staining revealed that only CMV-hOATP1B3-transfected HEK293 cells produced abundant OATP1B3, which localized at the cell membrane. OATP1B3 expression levels remained high through the 25th subculture cycle, but decreased substantially by the 50th subculture cycle. MRI of cell phantoms showed that only the CMV-hOATP1B3-transfected cells produced a significant contrast enhancement effect. In vivo MRI of xenograft tumors revealed that only CMV-hOATP1B3-transfected HEK293 tumors demonstrated a T1 contrast effect, which lasted for at least 5 hours. Conclusion: The human endogenous OATP1B3 gene can be non-virally delivered into cells to induce transient OATP1B3 expression, leading to gadoxetic acid-mediated enhancement on MRI. These results indicate that hOATP1B3 can serve as an MRI-reporter gene while minimizing the risk of long-term complications.

Pseudomonas sp. 의한 Benzoate와 m-Toluate 혼합물의 생분해 (Biodegradation of Mixture of Benzoate and m-Toluate with Pseudomonas sp.)

  • 정준영;김교창;조재민
    • 한국미생물·생명공학회지
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    • 제26권4호
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    • pp.352-357
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    • 1998
  • 방향족 화합물의 기본을 이루고 있는 benzoate와 m-toluate 혼합물 분해를 위한 45일간의 배양 결과 benzoate와 m-toluate 최적 기질 혼합비는 benzoate(75%): m-toluate(25%)일 때 가장 높은 균 생장율과 COD 제거율을 나타내었다. 또한 45일간의 배양 중 혼합기질의 농도가 2,000ppm으로 교체된 30일째의 benzoate와 m-toluate의 기질 분해율은 각각 94%와 79%였고 이때의 COD 제거율은 약 80%였다. 한편 효소 활성측정 결과 초기에 거의 검출되지 않았던 catechol 1,2-dioxygenase의 활성이 검출되어 m-toluate에 의해 본 균주의 효소 대사계가 유도 되었음을 알 수 있었다. 또한 배양 중 기질 농도에 대한 본 균주의 형태변화를 전자현미경으로 관찰한 결과, 기질의 농도가 높을수록 균 형태가 변화된 것으로 볼 때 일정 농도 이상의 방향족 화합물에 대한 내성은 대사에 관련된 효소 활성에 기인할 뿐만 아니라 아니라 세포벽 또는 세포막의 특성에 기인할 수도 있는 것으로 추측된다.

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Novel artesunate-metformin conjugate inhibits bladder cancer cell growth associated with Clusterin/SREBP1/FASN signaling pathway

  • Peiyu Lin;Xiyue Yang;Linghui Wang;Xin Zou;Lingli Mu;Cangcang Xu;Xiaoping Yang
    • The Korean Journal of Physiology and Pharmacology
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    • 제28권3호
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    • pp.219-227
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    • 2024
  • Bladder cancer remains the 10th most common cancer worldwide. In recent years, metformin has been found to have potential anti-bladder cancer activity while high concentration of IC50 at millimolar level is needed, which could not be reached by regular oral administration route. Thus, higher efficient agent is urgently demanded for clinically treating bladder cancer. Here, by conjugating artesunate to metformin, a novel artesunate-metformin dimer triazine derivative AM2 was designed and synthesized. The inhibitory effect of AM2 on bladder cancer cell line T24 and the mechanism underlying was determined. Anti-tumor activity of AM2 was assessed by MTT, cloning formation and wound healing assays. Decreasing effect of AM2 on lipogenesis was determined by oil red O staining. The protein expressions of Clusterin, SREBP1 and FASN in T24 cells were evaluated by Western blotting. The results show that AM2 significantly inhibited cell proliferation and migration at micromolar level, much higher than parental metformin. AM2 reduced lipogenesis and down-regulated the expressions of Clusterin, SREBP1 and FASN. These results suggest that AM2 inhibits the growth of bladder cancer cells T24 by inhibiting cellular lipogenesis associated with the Clusterin/SREBP1/FASN signaling pathway.