김태진 교수
Tae-jin Kim
성균관대학교 의학과 · 의학
연구실 소개
김태진 교수의 연구실은 장내 면역 반응과 미생물군의 상호작용을 중심으로, 병원성 미생물 제거를 위한 생리적 기전과 면역 세포의 활성화 경로를 규명하고 있습니다. 특히 곤충 모델(Drosophila)을 활용해 과산화물과 같은 반응성 산소종이 장내에서 어떻게 면역 반응을 유도하는지, 그리고 TRPA1 수용체와 같은 신호전달 수용체가 병원체 감지에 기여하는 메커니즘을 연구하고 있습니다. 또한 면역세포의 신호 전달 경로, 특히 MAPK 및 PI3K 경로를 통한 세포 반응 조절 메커니즘을 분석하며, 암 미세환경 내 면역세포의 기능적 역할도 탐색하고 있습니다.
연구 현황
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주요 논문
15Pathogen expulsion from the gut is an important defense strategy against infection, but little is known about how interaction between the intestinal microbiome and host immunity modulates defecation. In Drosophila melanogaster, dual oxidase (Duox) kills pathogenic microbes by generating the microbicidal reactive oxygen species (ROS), hypochlorous acid (HOCl) in response to bacterially excreted uracil. The physiological function of enzymatically generated HOCl in the gut is, however, unknown asid
A 120-kDa protein that is tyrosine-phosphorylated upon antigen receptor ligation in B lymphocytes has been identified as the product of the c-cbl protooncogene. Tyrosine phosphorylation of Cbl depends on the efficient association of membrane immunoglobulin heavy chains with the Ig alpha/beta heterodimer but is unimpaired in splenic B cells from the Xid mouse. Cross-linking of membrane IgM and membrane IgG, but not of CD40, leads to the tyrosine phosphorylation of Cbl. In receptor-ligated B lymph
The molecular basis for the modulatory properties of CD99 is not well understood. Treatment of human Jurkat T lymphocytes with anti-CD99 antibody led to activation of three mitogen-activated protein kinase (MAPK) members, ERK, JNK, and p38 MAPK, along with homotypic aggregation. While phosphorylation of ERK and JNK was inhibited by the pretreatment of a PKC inhibitor, bisindolylmaleimide I, activation of p38 MAPK was upregulated by the same pretreatment. The signaling pathways to MAPKs by CD99 e
The objective of this study is to describe the clinical outcomes of patients treated for cervical pregnancy with or without methotrexate (MTX) and to evaluate the effects of MTX in the treatment of cervical pregnancy. Between January 1993 and February 2000, 31 patients were diagnosed with cervical pregnancy. Twenty-two patients were treated with MTX chemotherapy and nine patients were treated with surgical procedures without MTX treatment. In the non-MTX treatment group, three patients underwent
EDITORIAL article Front. Immunol., 28 January 2020Sec. B Cell Biology Volume 11 - 2020 | https://doi.org/10.3389/fimmu.2020.00045
We have used a surface plasmon resonance biosensor (SPR, BIACORE 2000) to detect antibodies against glucose 6-phosphate isomerase (GPI) in synovial fluids of rheumatoid arthritis (RA) and osteoarthritis (OA). Recombinant human GPI proteins fused with or without NusA were expressed in E. coli, purified to homogeneity and immobilized in flow cells of CM5 sensor chips. The flow cells immobilized with NusA protein or bovine serum albumin were used to monitor non-specific binding. Synovial fluid samp
Large volumetric expansion and structural pulverization have been major problems in Si-based anode materials for Li-ion batteries. To overcome this limitation, yolk-shell structured Si-carbon structures have been proposed to allow for the reversible structural breathing of Si nanoparticles confined inside the carbon shell. However, initial coulombic efficiency (ICE) of the yolk-shell structured anodes is highly decreased mainly due to their extremely high specific surface area (SSA) and the resu
Glioblastoma multiforme (GBM) is clinically highly aggressive as a result of evolutionary dynamics induced by cross-talk between cancer cells and a heterogeneous group of immune cells in tumor microenvironment. The brain harbors limited numbers of immune cells with few lymphocytes and macrophages; thus, innate-like lymphocytes, such as γδ T cells, have important roles in antitumor immunity. Here, we characterized GBM-infiltrating γδ T cells, which may have roles in regulating the GBM tumor micro
Biophotons emitted from the center of fingernails and fingerprints from living humans are measured for twenty healthy subjects. We devised a dark box with a photo multiplier tube (H6180-01, Hamamatsu, Japan) whose spectral range is 300 nm to approximately 650 nm and a mount with a light-receiving hole of diameter 8 mm such that biophotons from the small circular area of nail or print of each finger are detected. Significantly more biophotons are emitted from fingernail than fingerprint for each
ENV motif of FcRL1 to provide a docking site for c-Abl, an SH2 domain-containing kinase. The FcRL1 and c-Abl signaling module, in turn, potently augmented B cell activation and proliferation. FcRL1-deficient mice exhibited markedly impaired formation of extrafollicular plasmablasts and germinal centers, along with decreased antibody production upon antigen stimulation. These findings reveal a critical BCR signal-enhancing function of FcRL1 through its intrinsic recruitment to B cell immunologica
Changes of glycosylation pattern in serum proteins have been linked to various diseases including cancer, suggesting possible development of novel biomarkers based on the glycomic analysis. In this study, N-linked glycans from human serum were quantitatively profiled by matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry (MS) and compared between healthy controls and ovarian cancer patients. A training set consisting of 40 healthy controls and 40 ovarian canc
We studied the role of lipid rafts and actin cytoskeleton in CD99-mediated signaling to elucidate the mechanism of protein transport upon CD99 engagement. CD99 engagement in Jurkat cells elicited the exocytic transport of GM1 as well as several surface molecules closely related with CD99 functions. In addition, CD99 molecules were rapidly incorporated into lipid rafts and appeared to rearrange the actin cytoskeleton upon CD99 stimulation. Association of CD99 with actin cytoskeleton was inhibited
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