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Dong-Sun Im

Kyung Hee University · Biochemistry, Genetics and Molecular Biology

About the Lab

Professor Dong-Sun Im's research lab specializes in molecular pharmacology and signal transduction, focusing on bioactive lipid mediators and their G protein-coupled receptors (GPCRs). The lab investigates sphingosine 1-phosphate and lysophosphatidic acid (LPA) receptors, particularly their roles in inflammation, neurodegeneration, and cellular signaling. A key area of research involves identifying and characterizing novel lipid-sensing GPCRs, such as Edg-8 and T cell death-associated gene 8, which mediate pathological responses in diseases like globoid cell leukodystrophy. The lab also explores the pharmacological mechanisms of traditional medicinal plants, especially ginseng, identifying novel bioactive components like gintonin that modulate GPCR pathways.

sphingosine 1-phosphatelysophosphatidic acidG protein-coupled receptorsginsengneuroinflammation

Research Overview

Papers
257
Total Citations
10,445
Papers (5y)
45
Primary Field
Biochemistry, Genetics and Molecular Biology

Research Output Trend

Figures are computed from collected data and may differ slightly.

Publications per year (5y)
45total
2021
2022
2023
2024
2025
Citations per year (5y)
402total
20212022202320242025

Selected Papers

15
1
Article|325 citations·2000
Characterization of a Novel Sphingosine 1-Phosphate Receptor, Edg-8
Dong‐Soon Im, Christopher E. Heise, Nicolas Ancellin, Brian F. O’Dowd, Gan-Ju Shei, R.P. Heavens, Michael R. Rigby, Timothy Hla, Suzanne Mandala, George McAllister, Susan R. George, Kevin R. Lynch
SJR Q1Journal of Biological ChemistryOA

Three G protein-coupled receptors (Edg-1, Edg-3, and Edg-5) for the lysolipid phosphoric acid mediator sphingosine 1-phosphate have been described by molecular cloning. Using a similar sequence that we found in the expressed sequence tag data base, we cloned and characterized of a fourth, high affinity, rat brain sphingosine 1-phosphate receptor, Edg-8. When HEK293T cells were co-transfected with Edg-8 and G protein DNAs, prepared membranes showed sphingosine 1- phosphate-dependent increases in

Molecular BiologyBiochemistry, Genetics and Molecular Biology
2
Article|226 citations·2004
Effects of ginsenosides Rg3 and Rh2 on the proliferation of prostate cancer cells
Hyun-Sook Kim, Eun‐Hee Lee, Sung‐Ryong Ko, Kang-Ju Choi, Jong-Hee Park, Dong‐Soon Im
SJR Q1Archives of Pharmacal Research
Molecular BiologyBiochemistry, Genetics and Molecular Biology
3
Review|210 citations·2020
Pro-Resolving Effect of Ginsenosides as an Anti-Inflammatory Mechanism of Panax ginseng
Dong‐Soon Im
SJR Q1BiomoleculesOA

, also known as Korean ginseng, is a famous medicinal plant used for the treatment of many inflammatory diseases. Ginsenosides (ginseng saponins) are the main class of active constituents of ginseng. The anti-inflammatory effects of ginseng extracts were proven with purified ginsenosides, such as ginsenosides Rb1, Rg1, Rg3, and Rh2, as well as compound K. The negative regulation of pro-inflammatory cytokine expressions (TNF-α, IL-1β, and IL-6) and enzyme expressions (iNOS and COX-2) was found as

Molecular BiologyBiochemistry, Genetics and Molecular Biology
4
Article|199 citations·2000
Molecular Cloning and Characterization of a Lysophosphatidic Acid Receptor, Edg-7, Expressed in Prostate
Dong‐Soon Im, Christopher E. Heise, Michael A. Harding, Susan R. George, Brian F. O’Dowd, Dan Theodorescu, Kevin R. Lynch
SJR Q1Molecular Pharmacology
Molecular BiologyBiochemistry, Genetics and Molecular Biology
5
Article|196 citations·2001
Identification of a Molecular Target of Psychosine and Its Role in Globoid Cell Formation
Dong‐Soon Im, Christopher E. Heise, Tuan Nguyen, Brian F. O’Dowd, Kevin R. Lynch
SJR Q1The Journal of Cell BiologyOA

Globoid cell leukodystrophy (GLD) is characterized histopathologically by apoptosis of oligodendrocytes, progressive demyelination, and the existence of large, multinuclear (globoid) cells derived from perivascular microglia. The glycosphingolipid, psychosine (d-galactosyl-beta-1,1' sphingosine), accumulates to micromolar levels in GLD patients who lack the degradative enzyme galactosyl ceramidase. Here we document that an orphan G protein-coupled receptor, T cell death-associated gene 8, is a s

Molecular BiologyBiochemistry, Genetics and Molecular Biology
6
Article|181 citations·1992
Partial purification of adeno-associated virus Rep78, Rep52, and Rep40 and their biochemical characterization
Dong‐Soon Im, Nicholas Muzyczka
SJR Q1Journal of VirologyOA

We have used differential cell extraction and conventional chromatography to separate and partially purify the four adeno-associated virus (AAV) nonstructural proteins Rep78, Rep68, Rep52, and Rep40. In the cytoplasmic extracts Rep52 and Rep40 were present in greater abundance than Rep68 and Rep78, with Rep78 being the least abundant. In nuclear extracts the four Rep proteins were approximately equal in abundance. Regardless of the subcellular fraction examined, three of the Rep proteins (Rep78,

GeneticsBiochemistry, Genetics and Molecular Biology
7
Review|158 citations·2012
Omega-3 fatty acids in anti-inflammation (pro-resolution) and GPCRs
Dong‐Soon Im
SJR Q1Progress in Lipid Research
BiochemistryBiochemistry, Genetics and Molecular Biology
8
Article|158 citations·1989
Factors that bind to adeno-associated virus terminal repeats
Dong‐Soon Im, Nicholas Muzyczka
SJR Q1Journal of VirologyOA

We have identified and characterized a DNA-protein complex that forms with the adeno-associated virus (AAV) terminal repeats. The complex formed only if the terminal palindrome was in the covalently closed or hairpin configuration; little if any binding was detected with the open duplex form of the terminal repeat. This fact suggested that both secondary structure and primary sequence are essential elements of recognition. DNase I protection studies indicated that virtually all of the A-A' palin

GeneticsBiochemistry, Genetics and Molecular Biology
9
Review|97 citations·2015
Functions of omega-3 fatty acids and FFA4 (GPR120) in macrophages
Dong‐Soon Im
SJR Q1European Journal of Pharmacology
Molecular BiologyBiochemistry, Genetics and Molecular Biology
10
Review|90 citations·2013
Yin and Yang of ginseng pharmacology: ginsenosides vs gintonin
Dong‐Soon Im, Seung‐Yeol Nah
SJR Q1Acta Pharmacologica SinicaOA

Ginseng, the root of Panax ginseng, has been used in traditional Chinese medicine as a tonic herb that provides many beneficial effects. Pharmacologic studies in the last decades have shown that ginsenosides (ginseng saponins) are primarily responsible for the actions of ginseng. However, the effects of ginseng are not fully explained by ginsenosides. Recently, another class of active ingredients called gintonin was identified. Gintonin is a complex of glycosylated ginseng proteins containing ly

Molecular BiologyBiochemistry, Genetics and Molecular Biology
11
Article|88 citations·2001
Characterization of the Human and Mouse Sphingosine 1-Phosphate Receptor, S1P5 (Edg-8): Structure−Activity Relationship of Sphingosine1-Phosphate Receptors
Dong‐Soon Im, Jeremy J. Clemens, Timothy L. Macdonald, Kevin R. Lynch
SJR Q1Biochemistry

Five G protein-coupled receptors (S1P(1)/Edg-1, S1P(3)/Edg-3, S1P(2)/Edg-5, S1P(4)/Edg-6, and S1P(5)/Edg-8) for the intercellular lipid mediator sphingosine 1-phosphate have been cloned and characterized. We found human and mouse sequences closely related to rat S1P(5) (97% identical amino acids) and report now the characterization of the human and mouse S1P(5) gene products as encoding sphingosine 1-phosphate receptors. When HEK293T cells were cotransfected with S1P(5) and G protein DNAs, prepa

Molecular BiologyBiochemistry, Genetics and Molecular Biology
12
Article|88 citations·2017
GPR35 mediates lodoxamide‐induced migration inhibitory response but not CXCL17‐induced migration stimulatory response in THP‐1 cells; is GPR35 a receptor for CXCL17?
Soo‐Jin Park, Seung Jin Lee, So‐Yeon Nam, Dong‐Soon Im
SJR Q1British Journal of PharmacologyOA

BACKGROUND AND PURPOSE: GPR35 has long been considered an orphan GPCR, because no endogenous ligand of GPR35 has been discovered. CXCL17 (a chemokine) has been reported to be an endogenous ligand of GPR35, and it has even been suggested that it be called CXCR8. However, at present there is no supporting evidence that CXCL17 does interact with GPR35. EXPERIMENTAL APPROACH: We applied two assay systems to explore the relationship between CXCL17 and GPR35. An AP-TGF-α shedding assay in GPR35 over-e

OncologyMedicine
13
Article|77 citations·2014
Sphingosine 1-phosphate induced anti-atherogenic and atheroprotective M2 macrophage polarization through IL-4
Soo‐Jin Park, Kyoung‐Pil Lee, Saeromi Kang, Jaewon Lee, Kōichi Sato, Hae Young Chung, Fumikazu Okajima, Dong‐Soon Im
SJR Q2Cellular Signalling
ImmunologyImmunology and Microbiology
14
Review|71 citations·1999
Life on the edg
Kevin R. Lynch, Dong‐Soon Im
SJR Q1Trends in Pharmacological Sciences
Molecular BiologyBiochemistry, Genetics and Molecular Biology
15
Article|71 citations·2009
Increase in sphingolipid catabolic enzyme activity during aging
Santosh J. Sacket, Hae‐Young Chung, Fumikazu Okajima, Dong‐Soon Im
SJR Q1Acta Pharmacologica SinicaOA
Molecular BiologyBiochemistry, Genetics and Molecular Biology

Research Areas

Molecular BiologyPhysiologyFood SciencePharmacologyImmunologyDermatology

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