김락균 교수
Nak-Kyun Kim
연세대학교 의생명과학부
연구실 소개
김락균 교수의 연구실은 면역세포의 노화와 관련된 면역기능 저하(면역노화)가 만성 폐질환, 특히 만성폐쇄성폐질환(COPD)의 발병 메커니즘과 어떻게 연관되는지 규명하는 데 초점을 맞추고 있습니다. 특히, 만성적인 저항성 염증 상태인 '인플라마징(inflammaging)'과 면역세포 기능 저하가 폐 조직에 미치는 영향을 분자생물학적·유전자 조절 수준에서 탐구하고 있습니다. 또한, 마이코박테리아 감염 시 면역 반응을 조절하는 신호전달 분자들(예: CD11b, Mincle)과 바이러스 감염에 대한 인터페론 반응 조절 메커니즘(예: OASL1, eRNA)에 이르기까지 면역 조절의 핵심 분자들을 규명하고 있습니다. 이와 더불어 간세포암에서의 염증 및 유전자 조절 네트워크를 연구하며, 질병의 기전을 밝히는 데 기여하고 있습니다.
연구 현황
연구 성과 추이
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
주요 논문
8Although chronic obstructive pulmonary disease (COPD) is regarded as a chronic inflammatory lung disease, the disease mechanismis still not known. Intriguingly, aging lungs are quite similar to COPD-affected lungs in many ways, and COPD has beenviewed as a disease of accelerated premature aging of the lungs. In this paper, based on a literature review, we would like to proposeimmunosenescence, age-associated decline in immunity, as a critical mechanism for the development of COPD. Immunosenescen
During mycobacteria infection, anti-inflammatory responses allow the host to avoid tissue damage caused by overactivation of the immune system; however, little is known about the negative modulators that specifically control mycobacteria-induced immune responses. Here we demonstrate that integrin CD11b is a critical negative regulator of mycobacteria cord factor-induced macrophage-inducible C-type lectin (Mincle) signaling. CD11b deficiency resulted in hyperinflammation following mycobacterial i
Oligoadenylate synthetase (OAS) protein family is the major interferon (IFN)-stimulated genes responsible for the activation of RNase L pathway upon viral infection. OAS-like (OASL) is also required for inhibition of viral growth in human cells, but the loss of one of its mouse homolog, OASL1, causes a severe defect in termination of type I interferon production. To further investigate the antiviral activity of OASL1, we examined its subcellular localization and regulatory roles in IFN productio
Cell type specification is a delicate biological event in which every step is under tight regulation. From a molecular point of view, cell fate commitment begins with chromatin alteration, which kickstarts lineage-determining factors to initiate a series of genes required for cell specification. Several important neuronal differentiation factors have been identified from ectopic over-expression studies. However, there is scarce information on which DNA regions are modified during induced pluripo
The complement is a part of the immune system that plays several roles in removing pathogens. Despite the importance of the complement system, the exact role of each component has been overlooked because the complement system was thought to be a nonspecific humoral immune mechanism that worked against pathogens. Decay-accelerating factor (DAF or CD55) is a known inhibitor of the complement system and has recently attracted substantial attention due to its role in various diseases, such as cancer
Enhancers have been conventionally perceived as cis-acting elements that provide binding sites for trans-acting factors. However, recent studies have shown that enhancers are transcribed and that these transcripts, called enhancer RNAs (eRNAs), have a regulatory function. Here, we identified putative eRNAs by profiling and determining the overlap between noncoding RNA expression loci and eRNA-associated histone marks such as H3K27ac and H3K4me1 in hepatocellular carcinoma (HCC) cell lines. Of th
Cells must fine-tune their gene expression programs for optimal cellular activities in their natural growth conditions. Transcriptional memory, a unique transcriptional response, plays a pivotal role in faster reactivation of genes upon environmental changes, and is facilitated if genes were previously in an active state. Hyper-activation of gene expression by transcriptional memory is critical for cellular differentiation, development, and adaptation. TREM (Transcriptional REpression Memory), a
Hepatocellular carcinoma is a major health burden, and thoughvarious treatments through much research are available, difficultiesin early diagnosis and drug resistance to chemotherapy-basedtreatments render several ineffective. Cancer stem cell model hasbeen used to explain formation of heterogeneous cell populationwithin tumor mass, which is one of the underlying causesof high recurrence rate and acquired chemoresistance, highlightingthe importance of CSC identification and understandingthe mol
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