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GSBSE

Molecular and Cellular Biology

Molecular and Cellular Biology seeks mechanistic understanding of broad aspects of development and disease, including cell signal transduction, stem cell fate determination, and tissue homeostasis at multiple levels that include intermolecular, cell-cell, tissue and organ function. Related research within the GSBSE ranges from basic developmental and disease processes in cell and animal models from zebrafish to mouse, to studies in humans, which emphasize vascular biology, stem cell biology, tissue development, homeostasis and pathology. Learn more >

Neuroscience

Neuroscience is an intrinsically broad discipline aimed at understanding large issues such as cognition, behavior, and neurological systems at levels that include the underlying anatomical and cellular circuits, and even the molecular events that control cell excitability, synaptic function, and development. Neuroscience research within the GSBSE ranges from psychology and psychometric studies in humans, to neuropharmacology and toxicology, to molecular genetics of neurodevelopment and neurodegenerative disease in model organisms. Learn more >

Biomedical Engineering

Biomedical Engineering may be defined as the application of engineering principles to promote and enhance the health and well-being of humans. Applications span the gamut of clinical, therapeutic and diagnostic arenas. Research strengths of the GSBSE include; artificial muscle, biomedical microdevices and microsystems, Lab-on-Chip, Biosensors, nanodevices and instruments, cell mechanics, robotic surgery, single molecule imaging, spectroscopy and microscopy of biological materials, and porous implants for tissue ingrowth. Learn more >

Toxicology

Toxicology is an applied discipline that incorporates and builds on a host of scientific disciplines to investigate the consequences of exposure to chemical agents on living organisms and the environment, and the cellular and molecular mechanisms that underlie those consequences. Research strengths of the GSBSE include; comparative marine toxicology, chemical carcinogenesis, immunotoxicology, toxicogenomics, neurotoxicology, and outer space toxicology. Learn more >

Bioinformatics and Computational Biology

Research in bioinformatics and computational biology is an interdisciplinary area of study that brings together biologists, computer and information scientists, mathematicians, engineers, biophysicists, and chemists to examine fundamental biological processes through data intensive analysis and computational modeling.
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Carol Kim

Carol Kim

Contact Information

Phone:
(207) 581-1505

Email/web:
carolkim@maine.edu

Address:
University of Maine
Department of Molecular and Biomedical Sciences 
Orono, ME  04469

Education

Ph.D. Cornell University

Research Interests

Cystic fibrosis (CF) is a complex, multi-system, autosomal recessive genetic disorder that affects approximately 30,000 children and adults in the United States and is caused by a mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel gene.  To date, over 1500 genetic mutations in the CFTR gene have been identified, but the most prevalent involves the deletion of three nucleotides encoding a phenyalanine at amino acid residue 508 (the so-called ΔF508 mutation).  Mutations in CFTR lead to issues in protein folding, gating, and/or stability.  In the absence of functional CFTR protein, fluid homeostasis is disrupted, causing the accumulation of mucus in affected organs including the lungs, pancreas, liver, and intestine.  Eighty percent of CF patients eventually develop chronic infections with Pseudomonas aeruginosa, giving rise to chronic inflammation of lung tissue, and ultimately leading to serious complications and death.

Recently, we described a powerful link among cftrP. aeruginosa, and innate immunity using the zebrafish model system to study this human disease.  To date, numerous animal models have been developed to study various aspects of CF; however, it is clear that no perfect animal model exist to study each of its disease manifestations.  The zebrafish CF model is particularly useful in understanding the linkage between the cftr gene and innate immunity.  We have previously shown that the loss of Cftr function leads to a compromised ability to clear a systemic infection by P. aeruginosa.  These effects were attributable to a diminished capacity to mount a respiratory burst response and to a diminished neutrophil migration response.

There is a growing interest in establishing CFTR gene/environment linkages.  Using our zebrafish model for human CF, we have recently shown that cftr and arsenic each mediate aspects of innate immunity.  In our current studies, we are establishing linkages that show how arsenic affects the innate immune response through Cftr function.  To accomplish this objective, we are deep sequencing the transcriptomes (RNA-seq and small RNA-seq) of zebrafish displaying a CF phenotype, exposed to arsenic at environmentally relevant doses (2 ppb and 10 ppb), and infected by P. aeruginosa.  From these data, we are generating gene lists that will identify potential target pathways affected by cftr function, arsenic exposure, and/or P. aeruginosa infection.   Our findings will enable us to characterize potential synergistic and antagonist interactions between the highly-conserved zebrafish cftr gene and the environmental toxicant arsenic, particularly in the context of a systemic infection with P. aeruginosa.  These data will enable us to identify critical pathways that will be targeted in subsequent experiments and subjected to further deep sequencing efforts.

Recent recognition of the intrinsic importance of the innate immune response—beyond its regulatory role in the subsequent adaptive immune response—suggests that this system plays a vital role in protection against infectious diseases.  This first response to infection, which includes the Toll-like receptor (TLR) mediated events, is crucial for fighting pathogen invasion and potentiating the adaptive immune response. Without a vigorous innate immune response, an effective adaptive immune response and a memory response for vaccines cannot be achieved.  My laboratory focuses on characterizing the innate immune pathways and determining ways in which the innate immune response can be activated, boosted, and prolonged using the zebrafish as our model system. The following are ongoing projects in my lab:

Characterization of Zebrafish Toll Signal Transduction Pathway

Recent recognition of the intrinsic importance of the innate immune response, in addition to its regulatory role in subsequent adaptive immunity, suggests that this system plays a crucial role in protection against agents of infectious disease. An important goal of my research is to better understand the innate immune response that acts through the Toll signal transduction pathway. Evidence supports the existence of Toll receptors, described as “pattern recognition receptors,” which have the ability to detect a variety of indicators of infectious organisms, and which feed into a common activation pathway. Activation of either the invertebrate or vertebrate signaling pathway results in a cascade of events that leads to the synthesis of antimicrobial/antifungal peptides or cytokines. Through molecular dissection of this pathway in the zebrafish, a vertebrate with a less complex immune system than that of mammals, we have made significant progress toward the identification of factors that influence regulation of the innate immune response and in turn regulate the adaptive immune response. Ultimately, we hope to apply our understanding of the Toll signaling pathway to the development of methods for intervention that can be applied to mammals and a range of fish species.

Role of CFTR in modulating resistance to bacterial infection

The zebrafish model system is being used to understand the relationship between the cystic fibrosis transmembrane conductance regulator (CFTR), the chloride channel linked to cystic fibrosis (CF) disease, and Pseudomonas aeruginosa infection.  CF is a lethal genetic disease caused by recessive mutations in the CFTR gene and is associated with prevalent and chronic P. aeruginosa lung infections. Despite the numerous studies that have sought to discover the role of CFTR in the innate immune response, it remains unclear how this affects P. aeruginosa infection.   Differences between the current cell culture and mouse CF model systems may account for some of the discrepancies that persist.

Zebrafish CFTR morphant embryos can be infected with P. aeruginosa, and we have shown that morphants exhibited an enhanced respiratory burst response, yet bacterial burdens at 8 hours post infection were found to be significantly higher in CFTR morphants than in controls.  This was confirmed visually using red fluorescent protein-labeled P. aeruginosa in MPO:GFP and Fli1:GFP transgenic zebrafish.  The ability of phagocytes to clear the infection was monitored by fluorescence microscopy in live embryos.  In addition, the formation of bacterial biofilms was observed during thePseudomonas infection, potentially contributing to the inability of the host to clear infection.  These studies underscore the importance of the zebrafish as an effective model for the innate immune response to P. aeruginosa infection in CF disease.

Caveolae and FPALM

Understanding spatial distribution and dynamics of receptors within unperturbed membranes is essential for elucidating their role in antiviral signaling.  Caveolae are cell membrane domains integral to numerous signaling pathways. We have recently shown a mechanism for virus evasion of host cell defenses through disruption of clusters of signaling molecules organized within caveolae.

Visualization of caveolae has previously been hampered by the inability to image these structures with sufficient resolution.  Limitations on spatial resolution imposed by diffraction in light microscopy rendered dynamic studies of the spatial localization of caveolae impossible.  Using repeated cycles of activation, localization, and bleaching of single photoactivatable fluorescent molecules, fluorescence photoactivation localization microscopy (FPALM) has achieved sub-diffraction resolution.

FPALM enabled the first single-molecule imaging of interactions between interferon antiviral signaling receptors (IFN-R) and caveolae (right). Knockdown of Caveolin-1, the protein that is the main component of caveolae, caused IFN-R clusters to disperse. Dispersal of IFN-R clusters led to a suppressed antiviral immune response through abrogation of downstream signaling, a response strongly suggesting that IFN-R organization within caveolae is critical for IFN-mediated antiviral defense.

Further studies are underway to investigate, at the single molecule level, the role of Caveolin-1 in the Toll-like Receptor pathway upstream from IFN-R. We are currently testing the hypothesis that caveolae also play a role in facilitating TLR9 signaling.

Selected Publications

In Press

  • Kortum, A.N., Rodriguez-Nunez, I., Yang, J., Shim, J., Runft, D., O'Driscoll, M.L., Haire, R.N., Cannon, J.P., Turner, P.M., Litman, R.T., Kim, C.H., Neely, M.N., Litman, G.W., Yoder, J.A. Differential expression and ligand binding indicate alternative functions for zebrafish polymeric immunoglobulin receptor (pIgR) and a family of pIgR-like (PIGRL) proteins. Immunogenetics.

Additional Publications

  • Gudheti, M. V., N.M. Curthoys, T.J. Gould, D. Kim, M.S. Gunewardene, K.A. Gabor, J.A. Gosse, C.H. Kim, J. Zimmerberg, and S.T. Hess. Actin mediates the nanoscale membrane organization of the clustered membrane protein influenza hemagglutinin. Biophys J. 104(10):2182-92.
  • Gabor, K.A., C.R. Stevens, M.J. Pietraszewski, T.J. Gould, S.H. Lam, Z. Gong, S.T. Hess, and C.H. Kim. Super resolution microscopy reveals that caveolin-1 is required for spatial organization of CRFB1 and subsequent antiviral signaling and zebrafish. PLoS ONE 8 (7): e68759. doi:10.1371/journal.pone.0068759
  • Gabor, K.A., C. Sullivan and C.H. Kim. Snakehead Rhabdovirus. Mononegaviruses of Veterinary Importance Vol I: Pathobiology and Molecular Diagnosis (Eds M. Munir). 337-351.
  • Goody, M. F., E. Peterman, C. Sullivan, C.H. Kim. Quantification of the Respiratory Burst Response as an Indicator of Immune Health in Zebrafish. J. Vis. Exp.12 (79). doi: 10.3791/5066
  • Milligan-Myhre K., Charette J.R., Phennicie R.T., Stephens W.Z., Rawls J..F, Guillemin K., Kim C.H. Study of host-microbe interactions in zebrafish. Methods Cell Biol 105: 87-116.
  • Singer, J. T., M. J. Sullivan, L. A. Porter, R. T. Phennicie, and C. H. Kim. 2010. Broad host range plasmids for red fluorescent protein labeling of Gram-negative bacteria for use in the zebrafish model system. Appl. Environ. Microbiol. 76:3467-74.
  • Phennicie, R.T., M.J. Sullivan, J.T. Singer, J.A. Yoder, C.H. Kim. 2010. Specific Resistance to Pseudomonas aeruginosa infection in zebrafish is mediated by the cystic fibrosis transmembrane conductance regulator. Infect Immun. 78:4542-50.
  • Sullivan, C., J. Charette, J. Catchen, C.R. Lage, G. Giasson, J.H. Postlethwait, P.J. Millard and C.H. Kim. 2009. The gene history of zebrafish tlr4a and tlr4b is predictive of their divergent functions. J. Immunol. 83:5896-908.
  • Sullivan, C., and C. H. Kim. 2008. Innate Immune System of the Zebrafish, Danio rerio. In Innate Immunity of Plants, Animals, and Humans. H. Heine, ed. 113-133.
  • Sullivan, C. and C.H. Kim. 2008. Zebrafish as a model for infectious disease and immune function. Fish Shellfish Immunol. 25:341-50.
  • Sullivan, C., J.H. Postlethwait, C.R. Lage, P.J. Millard, and C.H. Kim. 2007. Evidence for Evolving TICAM Function in Vertebrates. J. Immunol. 178:4517-27
  • Nayak, A.N, C.R. Lage, and C.H. Kim. 2007. Effects of Low Concentrations of Arsenic on the Innate Immune System of the Zebrafish (Danio rerio). Toxicol. Sci. 98:118-24.
  • Lage, C.R., A. Nayak, and C.H. Kim. 2006. Arsenic ecotoxicology and innate immunity. Integr. Comp. Biol. 46: 1040 - 1054
  • Millard, P.J., L.E. Bickerstaff, S.E. LaPatra, and C.H. Kim. 2006. Detection of infectious hematopoietic necrosis virus and infectious salmon anemia virus by molecular padlock amplification. J. Fish. Dis. 29:201-213.
  • Hermann, A.C. and C.H. Kim. 2005. Effects of arsenic on the zebrafish innate immune system. Mar. Biotechnol. 7:494-505.
  • Phelan, P.E., M.T. Mellon, and C.H. Kim. 2005. Functional characterization of full-length TLR3, IRAK-4, and TRAF6 in zebrafish (Danio rerio). Mol. Immunol. 42:1057-1071.
  • Phelan, P.E., M.E. Pressley, P.E. Witten, M.T. Mellon, S.L. Blake, and C.H. Kim. 2005. Characterization of snakehead rhabdovirus infection in the zebrafish, Danio rerio. J. Virol. 79:1842-1852.
  • Pressley , M.E. , P.E. Phelan, III, P.E. Witten, M.T. Mellon, and C.H. Kim. 2005. Pathogenesis and inflammatory response to Edwardsiella tarda Infection in the zebrafish. Dev. Comp. Immunol. 29:501-513.
  • Hermann, A.C, P.J. Millard, S.L. Blake, and C.H. Kim. 2004. Development of a respiratory burst assay using zebrafish kidneys and embryos. J. Immunol. Methods. 292:119-129.
  • Alonzo, M., C.H. Kim, M.C. Johnson, M.E. Pressley, and J.C. Leong. 2004. The NV gene of snakehead rhabdovirus (SHRV) is not required for pathogenesis and a heterologous glycoprotein can be incorporated into the SHRV envelope. J. Virol. 78:5875-5882.
  • Altmann, S.M., M.T. Mellon, M.C. Johnson, B.H. Paw, N.S. Trede, L.I. Zon and C.H. Kim. 2004. Cloning and characterization of an Mx gene and its corresponding promoter from the zebrafish, Danio rerio. Dev. Comp. Immunol. 28:295-306.
  • Paw, B.H, A.J. Davidson, Y. Zhou, L. Rong, S.J. Pratt, C. Lee, N.S. Trede, A. Brownlie, A. Donovan, E.C. Liao, J.M. Ziai, A.H. Drejer, W. Guo, C.H. Kim, B. Gwynn, L.L. Peters, M.N. Chernova, S.L. Alper, A. Zapata, S.N. Wickramasinghe, M.J. Lee, S.E. Lux, A. Fritz, J.H. Postlewait, L.I. Zon. 2003. Cell-specific mitotic defect and dyserythropoiesis associated with erythroid band 3 deficiency. Nat. Genet. 34:59-64.
  • Altmann, S.M., M.T. Mellon, D.L. Distel, and C.H. Kim. 2003. Molecular and functional analysis of an interferon gene from the zebrafish, Danio rerio. J. Virol. 77:1992-2002.


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Our Programs

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We offer 3 degree programs in five research focus areas. Learn more


UMaine The Jackson Laboratory Maine Medical Center Research Institute The Mount Desert Island Biological Laboratory University of Southern Maine University of New England
 
For more information about the program, please contact:
Tammy Crosby • 207-581-4654 • gsbse@maine.edu