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Tae-yeon Lim

Hanyang University · 生化学・遺伝学・分子生物学

研究室紹介

Professor Tae-yeon Lim's research lab focuses on respiratory diseases, particularly asthma and pulmonary fibrosis, with an emphasis on developing innovative therapeutic strategies using advanced drug delivery systems. The lab investigates the pathophysiological roles of environmental pollutants—such as diesel exhaust particles and ozone—in exacerbating airway inflammation and remodeling. A key research direction involves designing targeted nanocarriers, including exosome-mimetic polymersomes and polymer-based systems like PEI–isoprenaline, for efficient siRNA and gene delivery to lung cells. The lab also explores stem cell therapy and regenerative approaches, aiming to restore lung function in fibrotic and inflammatory lung conditions.

asthma therapygene deliverynanocarrierspulmonary fibrosissiRNA delivery

Research Overview

Papers
7
Total Citations
127
Papers (5y)
6
Primary Field
生化学・遺伝学・分子生物学

Research Output Trend

Figures are computed from collected data and may differ slightly.

Publications per year (5y)
6total
2011
2014
2016
2024
2025
Citations per year (5y)
102total
20112014201620242025

Selected Papers

7
1
Article|68 citations·2014
Therapeutic Use of Stem Cell Transplantation for Cell Replacement or Cytoprotective Effect of Microvesicle Released from Mesenchymal Stem Cell
최문환, 반태현, 임태연

Idiopathic pulmonary fibrosis (IPF) is the most common and severe type of idiopathic interstitial pneumonias (IIP), and which is currently no method was developed to restore normal structure and function. There are several reports on therapeutic effects of adult stem cell transplantations in animal models of pulmonary fibrosis. However, little is known about how mesenchymal stem cell (MSC) can repair the IPF. In this study, we try to provide the evidence to show that transplanted mesenchymal ste

2
Article|26 citations·2016
Long-Term Effects of Diesel Exhaust Particles on Airway Inflammation and Remodeling in a Mouse Model
김병곤, 이푸른하늘, 이신화, 김영은, 신미용, 강예나, 배성환, 김민정, 임태연, 박춘식, 장안수

Purpose: Diesel exhaust particles (DEPs) can induce and trigger airway hyperresponsiveness (AHR) and inflammation. The aim of this study was to investigate the effect of long-term DEP exposure on AHR, inflammation, lung fibrosis, and goblet cell hyperplasia in a mouse model. Methods: BALB/c mice were exposed to DEPs 1 hour a day for 5 days a week for 3 months in a closed-system chamber attached to a ultrasonic nebulizer (low dose: 100 μg/m3 DEPs, high dose: 3 mg/m3 DEPs). The control group was e

3
Article|25 citations·2005
Additive Effect of Diesel Exhaust Particulates and Ozone on Airway Hyperresponsiveness and Inflammation in a Mouse Model of Asthma
장안수, 최인선, Hajime Takizawa, 임태연, June-Hyuk Lee, 박성우, Choon-Sik Park
http://kmbase.medric.or.kr/Main.aspx?d=KMBASE&m=VIEW&i=0191120050200050759

Allergic airway diseases are related to exposure to atmospheric pollutants, which have been suggested to be one factor in the increasing prevalence of asthma. Little is known about the effect of ozone and diesel exhaust particulates (DEP) on the devel-opment or aggravation of asthma. We have used a mouse asthma model to deter-mine the effect of ozone and DEP on airway hyperresponsiveness and inflammation. Methacholine enhanced pause (Penh) was measured. Levels of IL-4 and IFN- were quantified in

4
Article|5 citations·2016
Exosome and Polymersome for Potential Theranostic Applications
임태연, 이근용

Nano-sized systems have been used extensively for the delivery of various therapeutics, such as pharmaceuticals, proteins, and nucleic acids. Exosomes are small extracellular vesicles secreted from parent cells by fusion of multivesicular late endosomes with the plasma membrane, which act as an intercellular communication mediator and contain bioactive molecules. Thus, exosomes may possess potential as a natural delivery system. Polymersomes are synthetic vesicles composed of external bilayers,

5
Article|2 citations·2025
Isoprenaline-Modified Polyethyleneimine as an Efficient Gene Delivery System for Targeted Asthma Therapy and Airway Remodeling Inhibition
Jiwon An, Moonhwan Choi, Sol Kim, Hyungkyung Yoon, An-Soo Jang, Sang-Kyung Lee, 임태연
https://spj.science.org/doi/pdf/10.34133/bmr.0136

This study introduces a novel gene delivery system, polyethyleneimine modified with isoprenaline (PEI–isoprenaline), to enhance targeted gene delivery in the context of asthma therapy and airway remodeling. In vitro investigations used Beas2B cells to assess the biocompatibility of isoprenaline, PEI–isoprenaline, and small interfering RNA (siRNA)/PEI–isoprenaline complexes, with cytotoxicity evaluations confirming their safety. The transfection efficiency of the siRNA/PEI–isoprenaline complex wa

6
Article|1 citations·2011
Alterations of Gene Expression by Beta-tricalcium Phosphate in Osteoblast-like MG63 Cells
Jae Yun Jeon, Tae Yun Im, Seung Hwan Jeon, Kyung Gyun Hwang, Chang Joo Park
SJR Q2Maxillofacial Plastic and Reconstructive Surgery
Molecular BiologyBiochemistry, Genetics and Molecular Biology
7
Article|0 citations·2024
Targeted siRNA delivery to lung epithelia reduces airway inflammation in a mouse model of allergic asthma
Irfan Ullah, 최효성, 최창선, 정건호, 정재욱, 윤경주, 허서윤, 이유종, 강은화, 김상헌, 윤호주, 임태연

Asthma is a chronic inflammatory disease triggered by allergic reactions in the bronchia. These reactions lead to swelling of mucous membranes, hypersecretion of mucus, and bronchoconstriction, resulting in a restricted opening of the lung airway. Allergic pulmonary inflammation and airway hyperresponsiveness are induced when Th2 cytokines, such as interleukin (IL)-4 and IL-13, bind to their cognate receptors on lung epithelial cells. Specifically, IL-13 stimulates inflammation through a multi-s

Research Areas

Molecular Biology

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