• 제목/요약/키워드: Migration Agent

검색결과 211건 처리시간 0.024초

Construction of Chimeric Human Epidermal Growth Factor Containing Short Collagen-Binding Domain Moieties for Use as a Wound Tissue Healing Agent

  • Kim, Dong-Gyun;Kim, Eun-Young;Kim, Yu-Ri;Kong, In-Soo
    • Journal of Microbiology and Biotechnology
    • /
    • 제25권1호
    • /
    • pp.119-126
    • /
    • 2015
  • Among the various human growth factors, epidermal growth factor (hEGF, consisting of 53 amino acids) has various effects on cell regeneration, stimulation of proliferation, migration of keratinocytes, formation of granulation tissues, and stimulation of fibroblast motility, which are important for wound healing. Owing to their multiple activities, EGFs are used as pharmaceutical and cosmetic agents. However, their low productivity, limited target specificity, and short half-life inhibit their application as therapeutic agents. To overcome these obstacles, we fused the collagen-binding domain (CBD) of Vibrio mimicus metalloprotease to EGF protein. About 18 or 12 amino acids (aa) (of the 33 total amino acids), which were essential for collagen-binding activity, were combined with the N- and C-termini of EGF. We constructed, expressed, and purified EGF (53 aa)-CBD (18 aa), EGF (53 aa)-CBD (12 aa), CBD (18 aa)-EGF (53 aa), and CBD (12 aa)-EGF (53 aa). These purified recombinant proteins increased the numbers of cells in treated specimens compared with non-treated specimens and control hEGF samples. The collagen-binding activities were also evaluated. Furthermore, CBD-hybridized hEGF induced phosphorylation of the EGF receptor. These results suggested that these fusion proteins could be applicable as small therapeutic agents in wound tissue healing.

Corosolic acid의 유방암세포 증식 및 전이에 미치는 영향 (Effect of corosolic acid on apoptosis and angiogenesis in MDA-MB-231 human breast cancer cells)

  • 손건호;황진현;김동하;조영은
    • Journal of Nutrition and Health
    • /
    • 제53권2호
    • /
    • pp.111-120
    • /
    • 2020
  • 본 연구는 인간 유래 유방 암세포 MDA-MB-231를 대상으로 CA에 의한 세포사멸, 세포 이동 및 침윤 효과를 조사하였다. 암세포의 증식 억제 효과는 CA 농도 의존적으로 증식률이 감소하는 것을 확인하였다. CA에 의한 apoptosis 양성 세포를 확인하기 위해 DAPI stain를 진행한 결과, CA 농도 의존적으로 죽은 세포를 확인하였다. MDA-MB-231 세포에서 CA에 의한apoptosis marker 단백질 발현 증가와 ROS production증가를 확인할 수 있었다. 또한 CA에 의한 MDA-MB-231의 세포 이동률이 유의적으로 감소하는 것을 확인하였다. 마지막으로 세포의 이동과 전이 능력 또한 CA를 처리한 군에서 통계적으로 감소하는 것을 확인하였다. 본 연구 결과를 통해서 CA의 암세포 증식률 억제, 세포사멸 증가, 그리고 세포 이동 및 전이 억제 효과가 나타나는 것을 확인했으며, 이 결과를 통해서 향후 유방암에 대한 항암제로 개발될 수 있는 가능성을 가지고 있는 것으로 사료된다.

Anti-metastatic Effects on B16F10 Melanoma Cells of Extracts and Two Prenylated Xanthones Isolated from Maclura amboinensis Bl. Roots

  • Siripong, Pongpun;Rassamee, Kitiya;Piyaviriyakul, Suratsawadee;Yahuafai, Jantana;Kanokmedhakul, Kwanjai
    • Asian Pacific Journal of Cancer Prevention
    • /
    • 제13권7호
    • /
    • pp.3519-3528
    • /
    • 2012
  • Inhibitory effects of Maclura amboinenesis Bl, one plant used traditionally for the treatment of cancers, on metastatic potential of highly metastatic B16F10 melanoma cells were investigated in vitro. Cell proliferation was assessed using the MTT colorimetric assay. Details of metastatic capabilities including invasion, migration and adhesion of B16F10 melanoma cells were examined by Boyden Chamber invasion and migration, scratch motility and cell attachment assays, respectively. The results demonstrated that n-hexane and chloroform extracts exhibited potent anti-proliferative effects (p<0.01), whereas the methanol and aqueous extracts had less pronounced effects after 24 h exposure. Bioactivity-guided chromatographic fractionation of both active n-hexane and chloroform extracts led to the isolation of two main prenylated xanthones and characterization as macluraxanthone and gerontoxanthone-I, respectively, their structures being identified by comparison with the spectral data. Interestingly, both exhibited potent effective effects. At non-toxic effective doses, n-hexane and chloroform extracts (10 and $30{\mu}g/ml$) as well as macluraxanthone and gerontoxanthone-I (3 and $10{\mu}M$) significantly inhibited B16F10 cell invasion, to a greater extent than $10{\mu}m$ doxorubicin, while reducing migration of cancer cells without cellular cytotoxicity. Moreover, exposure of B16F10 melanoma cells to high concentrations of chloroform ($30{\mu}g/ml$) and geratoxanthone-I ($20{\mu}M$) for 24 h resulted in delayed adhesion and retarded colonization. As insights into mechanisms of action, typical morphological changes of apoptotic cells e.g. membrane blebbing, chromatin condensation, nuclear fragmentation, apoptotic bodies and loss of adhesion as well as cell cycle arrest in the G1 phase with increase of sub-G1 cell proportions, detected by Hoechst 33342 staining and flow cytometry were observed, suggesting DNA damage and subsequent apoptotic cell death. Taken together, our findings indicate for the first time that active n-hexane and chloroform extracts as well as macluraxanthone and gerontoxanthone-I isolated from Maclura amboinensis Bl. roots affect multistep of cancer metastasis processes including proliferation, adhesion, invasion and migration, possibly through induction of apoptosis of highly metastatic B16F10 melanoma cells. Based on these data, M. amboinensis Bl. represents a potential candidate novel chemopreventive and/or chemotherapeutic agent. Additionally, they also support its ethno-medicinal usage for cancer prevention and/or chemotherapy.

Effect of remifentanil on pre-osteoclast cell differentiation in vitro

  • Jeon, Hyun-Ook;Choi, In-Seok;Yoon, Ji-Young;Kim, Eun-Jung;Yoon, Ji-Uk;Cho, Ah-Reum;Kim, Hyung-Joon;Kim, Cheul-Hong
    • Journal of Dental Anesthesia and Pain Medicine
    • /
    • 제18권1호
    • /
    • pp.9-17
    • /
    • 2018
  • Background: The structure and function of bone tissue is maintained through a constant remodeling process, which is maintained by the balance between osteoblasts and osteoclasts. The failure of bone remodeling can lead to pathological conditions of bone structure and function. Remifentanil is currently used as a narcotic analgesic agent in general anesthesia and sedation. However, the effect of remifentanil on osteoclasts has not been studied. Therefore, we investigated the effect of remifentanil on pre-osteoclast (pre-OCs) differentiation and the mechanism of osteoclast differentiation in the absence of specific stimulus. Methods: Pre-OCs were obtained by culturing bone marrow-derived macrophages (BMMs) in osteoclastogenic medium for 2 days and then treated with various concentration of remifentanil. The mRNA expression of NFATc1 and c-fos was examined by using real-time PCR. We also examined the effect of remifentanil on the osteoclast-specific genes TRAP, cathepsin K, calcitonin receptor, and DC-STAMP. Finally, we examined the influence of remifentanil on the migration of pre-OCs by using the Boyden chamber assay. Results: Remifentanil increased pre-OC differentiation and osteoclast size, but did not affect the mRNA expression of NFATc1 and c-fos or significantly affect the expression of TRAP, cathepsin K, calcitonin receptor, and DC-STAMP. However, remifentanil increased the migration of pre-OCs. Conclusions: This study suggested that remifentanil promotes the differentiation of pre-OCs and induces maturation, such as increasing osteoclast size. In addition, the increase in osteoclast size was mediated by the enhancement of pre-OC migration and cell fusion.

Lycopene의 새로운 혈관내피세포 생리활성 (Novel Function of Lycopene in Vascular Endothelial Cell)

  • 조진구;김성현;서정화;안선영;정은실;박헌용
    • 생명과학회지
    • /
    • 제20권7호
    • /
    • pp.1093-1099
    • /
    • 2010
  • 항암 효과와 항산화 기능을 가지는 것으로 알려진 lycopene은 심혈관에서의 기능이 현재까지 잘 알려져 있지 않다. 본 연구에서는 lycopene의 심혈관 기능을 알기 위해 혈관내피세포를 이용해 다양한 세포실험을 수행하였다. 그 결과, lycopene은 내피세포의 성장 및 이동을 촉진하였으나 세포사멸에는 영향이 없었다. 또한, 백혈구의 혈관내피세포 부착을 억제하였고 내피세포 내 신호전달물질인 MAPK들의 활성을 촉발하였다. MAPK의 활성 억제제를 이용한 신호전달기전 연구실험 결과, ERK와 p38 MAPK의 활성은 세포성장에 관여하고, JNK의 활성은 세포이동에 관여함을 확인하였다. 종합하면, lycopene은 혈관내피세포의 신호전달 물질인 MAPK들를 통해 세포성장 및 이동을 촉진시키며, LPS에 의한 THP-1의 내피세포 부착을 억제 하는 등 혈관내피세포의 다양한 생리활성을 조절한다. Lycopene의 이러한 혈관내피세포 기능들은 lycopene이 혈관질환 치료제로 응용될 가능성이 있음을 의미한다.

Betulinic Acid Inhibits LPS-Induced MMP-9 Expression by Suppressing NF-kB Activation in BV2 Microglial Cells

  • Lee, Jae-Won;Choi, Yong-Joon;Kim, Song-In;Lee, Sue-Young;Kang, Sang-Soo;Kim, Nam-Ho;Kwon, Yong-Soo;Lee, Hee-Jae;Chun, Wan-Joo;Kim, Sung-Soo
    • Biomolecules & Therapeutics
    • /
    • 제19권4호
    • /
    • pp.431-437
    • /
    • 2011
  • Aberrant activation of microglia has been reported to cause neuronal damages by releasing a variety of pro-inflammatory cytokines. Besides where microglia become active, damages have been also observed in remote places, which is considered due to the migration of activated microglia. Therefore, an agent that could suppress abnormal activation of microglia and their subsequent migration might be valuable in activated microglia-related brain pathologies. The objective of the present study was to evaluate anti-inflammatory effects of betulinic acid on lipopolysaccharide (LPS)-stimulated BV2 microglial cells. Pretreatment of betulinic acid significantly attenuated LPS-induced NO production and protein expression of iNOS. Betulinic acid also significantly suppressed LPS-induced release and expression of cytokines such as TNF-${\alpha}$ and IL-$1{\beta}$. Furthermore, betulinic acid significantly uppressed LPS-induced MMP-9 expression, which has been suggested to play an important role in the migration of activated microglia. In order to understand the possible mechanism by which betulinic acid suppresses LPS-induced cytokine production and migration of microglia, the role of NF-kB, a major pro-inflammatory transcription factor, was examined. Betulinic acid significantly suppressed LPS-induced degradation of IKB, which retains NF-kB in the cytoplasm. Therefore, nuclear translocation of NF-kB upon LPS stimulation was significantly suppressed with betulinic acid. Taken together, the present study for the first time demonstrates that betulinic acid possesses anti-inflammatory activity through the suppression of nuclear translocation of NF-kB in BV2 microglial cells.

순수 P2P 네트워크 환경에서 에이전트 이주를 위한 자원 예약 기반 동적 부하 균형 기법 (Dynamic Load Balancing Scheme Based on Resource Reservation for Migration of Agents in Pure P2P Network Environments)

  • 김경인;김영진;엄영익
    • 정보처리학회논문지A
    • /
    • 제11A권4호
    • /
    • pp.257-266
    • /
    • 2004
  • 이동 에이전트는 자율성을 가지고 비동기적으로 수행이 가능한 개체로, 네트워크상의 여러 호스트들을 이동하면서 사용자를 대신해 특정한 작업을 수행하고 다른 에이전트들과 상호 협력할 수 있는 프로세스로 정의된다. 현재 이동 에이전트는 전자 상거래, 이동 통신, 병렬처리, 정보의 검색 및 복구 둥 여러 분야에서 사용된다. 그러나 순수 P2P 환경에서 컴퓨팅 자원을 사용하고자 하는 이동 에이전트들이 이주할 피어의 가용한 자원을 고려하지 않고 이주할 경우, 이주된 에이전트로 인해 해당 시스템의 부하가 증가 된다는 문제점이 발생하게 된다. 이러한 문제점을 해결하기 위해 본 논문에서는 각 피어들에 상주하는 자원 관리 에이전트를 이용하여 부하 정보를 모니터링 하고 이주할 에이전트와 목적지 피어를 결정하게 된다. 이동 에이전트가 이주하는 과정에서 특정 피어의 자원이 예약 선점 되었을 경우 해당 자원이 다른 에이전트에게 할당되는 것을 방지하는 자원 예약 기법을 기반으로 피어들 간의 균형 있는 이주 기법을 제안한다.

A Novel Anti-cancer Agent, SJ-8029, Inhibits Angiogenesis and Induces Apoptosis

  • Yi Eui-Yeun;Jeong Eun-Joo;Song Hyun-Seok;Kang Dong-Wook;Joo Jeong-Ho;Kwon Ho-Seok;Lee Sun-Hwan;Park Si-Kyung;Chung Sun-Gan;Cho Eui-Hwan;Kim Yung-Jin
    • 대한의생명과학회지
    • /
    • 제12권3호
    • /
    • pp.161-170
    • /
    • 2006
  • A new piperazine derivative, 8J-8029, is a synthetic anti-cancer agent which exhibits both microtubule and topoisomerase II inhibiting activities. In this study, we investigated the ability of 8J-8029 for anti-angiogenesis and apoptosis. 8J-8029 decreased the bFGF-induced angiogenesis in the CAM and the mouse Matrigel implants, in vivo. 8J-8029 inhibited the proliferation, migration, invasion, tube fonnation, and expression of MMP-2 in BAECs. In addition, 8J-8029 reduced the cell viability in HepG2 cells, caused the production of fragmented DNA and the morphological changes corresponding to apoptosis. 8J-8029 also elicited the release of cytochrome c and the activation of caspase-3. Taken together, these results suggest 8J-8029 may be a candidate for anti-cancer agent with the ability to inhibit the angiogenesis of endothelial cells and to induce the apoptosis of tumor cells.

  • PDF

Use of Imaging Agent to Determine Postoperative Indwelling Epidural Catheter Position

  • Uchino, Tetsuya;Hagiwara, Satoshi;Iwasaka, Hideo;Kudo, Kyosuke;Takatani, Junji;Mizutani, Akio;Miura, Masahiro;Noguchi, Takayuki
    • The Korean Journal of Pain
    • /
    • 제23권4호
    • /
    • pp.247-253
    • /
    • 2010
  • Background: Epidural anesthesia is widely used to provide pain relief, whether for surgical anesthesia, postoperative analgesia, treatment of chronic pain, or to facilitate painless childbirth. In many cases, however, the epidural catheter is inserted blindly and the indwelling catheter position is almost always uncertain. Methods: In this study, the loss-of-resistance technique was used and an imaging agent was injected through the indwelling epidural anesthesia catheter to confirm the position of its tip and examine the migration rate. Study subjects were patients scheduled to undergo surgery using general anesthesia combined with epidural anesthesia. Placement of the epidural catheter was confirmed postoperatively by injection of an imaging agent and X-ray imaging. Results: The indwelling epidural catheter was placed between upper thoracic vertebrae (n = 83; incorrect placement, n = 5), lower thoracic vertebrae (n = 123; incorrect placement, n = 5), and lower thoracic vertebra-lumbar vertebra (n = 46; incorrect placement, n = 7). In this study, a relatively high frequency of incorrectly placed epidural catheters using the loss-of-resistance technique was observed, and it was found that incorrect catheter placement resulted in inadequate analgesia during surgery. Conclusions: Although the loss-of-resistance technique is easy and convenient as a method for epidural catheter placement, it frequently results in inadequate placement of epidural catheters. Care should be taken when performing this procedure.

모세관 전기 영동을 이용한 퀴놀린계 항생제의 광학 이성질체 분석 (Chiral Separation of Quinolone Antibacterial Agent by Capillary Electrophoresis)

  • 강대천;조승일;정두수;최규성;김용성
    • 대한화학회지
    • /
    • 제46권5호
    • /
    • pp.412-429
    • /
    • 2002
  • (+)(18crown6)-tetracarboxylic acid ($18C6H_4$)를 퀴놀린계 항생제인 gemifloxacin을 모세관 전기영동법으로 키랄 분리하였다. Body fluid에서 퀴놀린계 항생제인 gemifloxacin의 직접적인 분석은 빠른 분석 시간, 다성분 분석등의 여러 가지 장점을 가진다. 그러나 Body fluid내의 높은 농도의 나트륨 이온은 $18C6H_4$와 강한 전하 상호작용으로 인하여 gemifoxacin과 $18C6H_4$의 상호작용을 방해한다. 키랄 선택제와 나트륨 이온 사이의 상호 작용을 줄이기 위해 완충 용액에 킬레이트 리간드 EDTA를 첨가하였다. 시료 용액에 150mM의 나트륨 이온이 존재 할 때에도 분리 효율의 향상과 이동 시간의 감소를 관찰 할 수 이었다.