최민이 교수
Minee-Liane Choi
KAIST 뇌인지과학과 · 생화학·유전·분자생물학
연구실 소개
최민이 교수의 연구실은 해마의 신경 발생과 뇌의 기억 기능, 특히 패턴 분리 기전에 초점을 맞추고 있으며, 신경세포 생성이 공간 기억 및 인식 능력에 미치는 영향을 동물 모델을 통해 규명하고 있습니다. 또한 파킨슨병과 같은 신경 퇴행성 질환에서 성질화된 아교세포의 염증 반응과 RNA 편집 메커니즘의 역할을 인간 induced pluripotent stem cell(ipsC)을 활용해 연구하고 있습니다. 산화 스트레스, 세포 사멸, 단백질 축적 등 신경세포 손상의 분자 기전을 실시간 세포 영상과 생화학적 분석을 통해 탐색하고 있습니다.
연구 현황
연구 성과 추이
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
주요 논문
12The dentate gyrus (DG) of the mammalian hippocampus is hypothesized to mediate pattern separation-the formation of distinct and orthogonal representations of mnemonic information-and also undergoes neurogenesis throughout life. How neurogenesis contributes to hippocampal function is largely unknown. Using adult mice in which hippocampal neurogenesis was ablated, we found specific impairments in spatial discrimination with two behavioral assays: (i) a spatial navigation radial arm maze task and (
RNA editing is a posttranscriptional mechanism that targets changes in RNA transcripts to modulate innate immune responses. We report the role of astrocyte-specific, ADAR1-mediated RNA editing in neuroinflammation in Parkinson's disease (PD). We generated human induced pluripotent stem cell-derived astrocytes, neurons and cocultures and exposed them to small soluble alpha-synuclein aggregates. Oligomeric alpha-synuclein triggered an inflammatory glial state associated with Toll-like receptor act
This protocol describes a method to perform calcium imaging with Fura-2 (live-cell imaging)
ABSTRACT Human induced pluripotent stem cells (hiPSCs) aim to replicate the developmental and functional capacity of human embryonic stem cells (hESCs). Here, we identify neuronal resilience under metabolic stress as a critical parameter for benchmarking equivalence. Without medium replenishment, hESC-derived cortical neurons underwent neural resurrection —a spontaneous recovery marked by increased cell density, preserved morphology, and sustained calcium signaling and mitochondrial function for
This protocol describes the method to perform patch-clamp recordings of iPSC-derived neurons.
This protocol describes a method of generating aggregation of human recombinant alpha-synuclein.
Abstract Mitochondrial dysfunction is a convergent hallmark of neurodegenerative diseases and represents a promising biomarker for early diagnosis and therapy. However, current in vitro assays rely on fluorescence or electron microscopy, which are invasive, low-throughput, and incompatible with longitudinal analysis. Here, we present a noninvasive framework by integrating label-free optical diffraction tomography (ODT) with organelle-aware representation learning to detect subtle mitochondrial d
This is a modified protocol that describes how to generate cortical region-specific astrocytes based on Gupta et al., 2012, Serio et al., 2013 and Seto-Salvia et al., 2021
This protocol contains instructions for examining cell death in live-cell imaging.
This protocol details the packaging of plasmids that are on a lentivirus backbone into a lentiviral construct, as well as cell transduction.
This protocol contains the instruction for measuring superoxide using dihydroethidium (HEt) which allows the rate of superoxide generation to be measured which is present as the ratio of the oxidized form of the dye over the reduced form. HEt allows the rate of cytosolic superoxide generation to be measured, by the slope of the ratio of oxidized dye to reduced dye.
This protocol details the packaging of plasmids that are on a lentivirus backbone into a lentiviral construct, as well as cell transduction.
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