
Kiwook Kim, PhD
Assistant Professor
Department of Pharmacology & Regenerative Medicine
Contact
Building & Room:
909 S Wolcott
Office Phone:
Email:
Related Sites:
Lab
Building & Room:
4160 COMRB
About
Research Interests
Mononuclear phagocytes consist of monocytes, dendritic cells and macrophages. They contribute to tissue homeostasis in steady state and orchestrate immune response in a pathological condition. In the past decade, there has been a dramatic progress in our understanding of development and function of mononuclear phagocytes. By generating constitutive- and tamoxifen inducible- Cre mice driven by CX3CR1 promoter, we previously revealed most tissue resident macrophages are derived from embryonic precursors (Immunity, 38: 79-91, 2013). Also, we demonstrated a minor population of tissue-resident macrophages can be replenished by circulating blood monocytes after birth (JEM, 213: 1951-1959, 2016).
Our lab investigates development and physiological roles of mononuclear phagocytes in steady state as well as pathological conditions (both inflammatory phase and resolving-phase) taking advantage of cutting-edge lineage-tracing approaches, cell ablation strategy and in-vivo imaging techniques combined with high throughput transcriptomic analysis.
Specifically, we focus on (1) roles of two monocyte populations (Ly6Chi CX3CR1int and Ly6Clo CX3CR1hi subsets) in either promoting or resolving the inflammation, (2) transition of monocytes to macrophage/dendritic cells and their impact on inflammation/ tissue repair, and (3) distinct roles of embryonic-derived macrophages and monocyte-derived macrophages in a variety of physiological or pathological conditions.
Postdoctoral & Lab Technician positions currently available. Please send CVs to kiwook@uic.edu
Selected Grants
NIH, The role of membrane-associated macrophages in health and inflammation (R01DK126753), PI
NIH, Macrophage Plasticity in Inflammatory Lung Injury (P01HL151317), PI
Selected Publications
Unravelling monocyte functions: from the guardians of health to the regulators of disease (Mildner, Kim and Yona, Discov Immunol, 2024)
LYVE1+ macrophages of murine peritoneal mesothelium promote omentum-independent ovarian tumor growth. (Zhang and Kim et al., J. Exp. Med., 2021)
MHC II+ resident peritoneal and pleural macrophages rely on IRF4 for development from circulating monocytes (Kim et.al., J. Exp. Med., 2016)
Fate mapping reveals origins and dynamics of monocytes and tissue macrophages under homeostasis (Yona and Kim et al., Immunity, 2013)
In vivo structure/function and expression analysis of the CX3C chemokine fractalkine (Kim et al, Blood, 2011)
Education
B.S., Handong Global University, S. Korea; Biomedical Science (2004).
M.S., Handong Global University, S. Korea; Cell biology (2007).
PhD, Weizmann Institute of Science, Israel; Immunology (2011).
Postdoc, Yale University School of Medicine, New Haven; Microbial Pathogenesis (2014).
Postdoc, Washington University School of Medicine, St. Louis; Pathogenesis & Immunology (2019).
Professional Memberships
American Association of Immunologists (AAI)
European Macrophage/DC Society (EMDS)
Research Currently in Progress
- Heterogeneity, Origins, and role of Macrophages in Health and Inflammation.
- Macrophage, DC, and monocytes-mediated cytokine regulation
- Commensal microbiota-Immune cell interaction
- Stromal cell (fibroblasts/epithelial cells)- Immune cell interaction