Jae Myun Lee
연세대학교 의과대학 · 의학
Jae Myun Lee 교수의 연구실은 바이러스 감염과 면역조절, 특히 에피스타트바이러스(EBV)가 숙주 세포에 미치는 영향에 중점을 두고 있습니다. EBNA2 단백질이 Notch 신호 경로를 모방하며 세포 증식을 유도하고, Nur77 단백질과의 상호작용을 통해 세포 사멸을 억제하는 메커니즘을 규명하고 있습니다. 또한 항우울제의 약물 반응에 영향을 미치는 MRP1 유전자 다형성과 암 미세환경에서 자연살해세포(NK cell) 기능 저하의 원인을 탐구하며, 바이오안전 및 백신 전달 시스템 개발에도 기여하고 있습니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
Epstein-Barr virus infection in vitro immortalizes primary B cells. EBNA2 is an Epstein-Barr virus-encoded transcriptional transactivator that mimics the effects of activated Notch signaling and is essential for this proliferative response. An assay using Sindbis virus (SV) as a cell death inducer revealed that, like Notch, EBNA2 also has antiapoptotic activity. We show that Nur77 is a mediator of SV-induced cell death and that EBNA2 antiapoptotic activity results from interaction with Nur77. EB
Reduction of CD56(bright) cells may precede NK cell dysfunction, leading to impaired cytotoxicity against PCa cells. These observations may explain one of the mechanisms behind NK cell dysfunction observed in PCa microenvironment and lend support to the development of future cancer immunotherapeutic strategies.
Although smallpox has been eradicated globally, the potential use of the smallpox virus in bioterrorism indicates the importance of stockpiling smallpox vaccines. Considering the advantages of microneedle-based vaccination over conventional needle injections, in this study, we examined the feasibility of microneedle-based smallpox vaccination as an alternative approach for stockpiling smallpox vaccines. We prepared polylactic acid (PLA) microneedle array patches by micromolding and loaded a seco
The replication of flaviviruses results in the secretion of four virus-coded proteins into the extracellular environment. Three of these proteins, E, C and M (or pre-M), are found in purified virions. A fourth virus-specified extracellular protein which was not present in either the slowly sedimenting haemagglutinin particles or in virions is described. The relationship of this protein to the intracellular NS1 polypeptide was investigated along with its similarity to the soluble complement-fixin
Multidrug resistance protein 1 (MRP1, ABCC1) transports antidepressive agents in the endothelial cells of the blood-brain barrier. Therefore, polymorphisms in the MRP1 gene may affect the treatment response of antidepressants. This study was aimed to identify the association between genetic variations in MRP1/ABCC1 and the therapeutic response to the antidepressant citalopram. One hundred and twenty-three patients who had been treated with citalopram monotherapy to control their major depressive
In addition to functioning as a transcriptional transactivator, Epstein-Barr virus EBNA2 interacts with Nur77 to protect against Nur77-mediated apoptosis. Estrogen-regulated EBNA2 in EREB2-5 cells was replaced by either EBNA2 or EBNA2 with a deletion of conserved region 4 (EBNA2DeltaCR4). Both EBNA2-converted and EBNA2DeltaCR4-converted EREB2-5 cells grew in the absence of estrogen and expressed LMP1. Treatment with tumor necrosis factor alpha did not induce apoptosis of EBNA2- or EBNA2DeltaCR4-
In this paper, we study multirate transversal adaptive digital filters (ADF's) based on the block least-mean-square (BLMS) algorithms. These include an ADF with decimation (ADFD) and an ADF with interpolation (ADFI). We first formulate these filters based on the block mean-squared error (BMSE) criterion and derive BLMS multi-rate weight-adjustment algorithms, and then study efficient realization of those filters. It is shown that the BLMS ADFD can be realized efficiently in the direct form or in