Minsoo Kim, Ph.D.

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Contact

University of Rochester
School of Medicine and Dentistry
601 Elmwood Ave, Box 609
Rochester, New York 14642

Lab: 585 273-1435 (primary)

Fax: 585 273-2452

Portrait

Unlike cells within solid tissues, circulating leukocytes relocate during the course of immune reactions and dynamically adhere and de-adhere to cells of the vasculature and to other immune cells, as well as to components of the extracellular matrix. A subset of integrins (LFA-1, Mac-1, and VLA4) are expressed on leukocytes and play a major role in regulating leukocyte adhesion and recruitment to damaged or infected tissues during inflammatory responses. The activity of integrins to bind ligands is dynamically and tightly regulated through conformational changes from inactive form to the active one that binds ligands with high affinity. Under a wide range of pathologic conditions, these mechanisms of integrin activation are mis-regulated resulting in abnormal leukocyte trafficking, and direct damage to the vasculature and the underlying tissue making leukocyte integrins a promising therapeutic target for anti-inflammation therapy. Therefore, it would be critical to understand how integrins and their ligands bind to one another, the flow of conformational changes from one integrin domain to another, and the connections to other signaling molecules.

In order to visualize the conformational changes in integrin LFA-1 and its dynamic redistribution on the plasma membrane, we applied the quantitative imaging technique FRET (fluorescence resonance energy transfer) to living cells. Our current research focuses on integrin-mediated leukocyte migration during inflammation. By employing advanced imaging techniques including FRET, live cell imaging, 3D confocal-image reconstruction, IRM (interference reflection microscopy), and TIRFM (total internal reflection fluorescence microscopy), we are trying to improve our understanding of the supramolecular/architectural properties of leukocyte integrins with particular emphasis on their relationship with leukocyte migration. In addition, we are interested in visualizing dynamic interactions of intracellular signaling molecules and identifying new molecules that regulate integrin activation during the leukocyte chemotaxis.

Current Appointments

Education
PhD Pharmacology Ohio State University 2001
BS Genetic Engineering Korea-Korea University 1993
Post-Doctoral Training & Residency
Center for Blood Research, Harvard Medical School, Boston, MA 2001 - 2004

Lab Website

http://www.urmc.rochester.edu/labs/Kim-Lab/


Recent Journal Articles
Showing the 5 most recent journal articles. (22 available)
Hyun YM; Lefort CT; Kim M. "Leukocyte integrins and their ligand interactions." Immunologic research. 2009; Epub 2009 Jan 29.
Elphick GF; Sarangi PP; Hyun YM; Hollenbaugh JA; Ayala A; Biffl WL; Chung HL; Rezaie AR; McGrath JL; Topham DJ; Reichner JS; Kim M. "Recombinant human activated protein C inhibits integrin-mediated neutrophil migration." Blood. 2009; 113(17):4078-85. Epub 2009 Feb 24.
Quinn JA; Graeber CT; Frackelton AR; Kim M; Schwarzbauer JE; Filardo EJ. "Coordinate regulation of estrogen-mediated fibronectin matrix assembly and epidermal growth factor receptor transactivation by the G protein-coupled receptor, GPR30." Molecular endocrinology (Baltimore, Md.). 2009; 23(7):1052-64. Epub 2009 Apr 02.
Hyun YM; Chung HL; McGrath JL; Waugh RE; Kim M. "Activated integrin VLA-4 localizes to the lamellipodia and mediates t cell migration on VCAM-1." Journal of immunology (Baltimore, Md. : 1950). 2009; 183(1):359-69.
Lefort CT; Hyun YM; Schultz JB; Law FY; Waugh RE; Knauf PA; Kim M. "Outside-In Signal Transmission by Conformational Changes in Integrin Mac-1." Journal of immunology (Baltimore, Md. : 1950). 2009; Epub 2009 Oct 28.