Christine McGahan, PhD
Department Head, Molecular Biomedical Sciences
Post-doctoral: 1981-2, Harkness Eye Institute, Columbia University College of Physicians and Surgeons. Mentor, Dr. Laszlo Bito
AffiliationsTreasurer, International Society for Eye Research, 2012-Present
Association for Research in Vision and Ophthalmology
Member, National Advisory Eye Council, 2007-2011
RECENT PRESENTATIONS AT MEETINGS
- McGahan, M.C., M. Lall, J. Ferrell, M. Goralska, L. Fleisher, S. Nagar, J. Harned. 2010. Iron regulated gene expression trough control of hypoxia-inducible factor-1. Invited Paper for the XIX International Society for Eye Research meeting, Montreal in July, 2010.
- McGahan, M.C., M. Goralska, L.N. Fleisher, M. Lall, S. Nagar, P. Mzyk, J. Harned. 2011. Hypoxia increases glutamate secretion by retinal pigmented epithelial cells. Invest. Ophthalmol. Vis. Sci. (Suppl.) Abstract # 890
- McGahan, M.C., S. Nagar, M. Goralska, L.N. Fleisher, J. Harned. 2012. Transepithelial iron transport and polarized iron reuptake in retinal pigmented epithelial cells. Invest. Ophthalmol. Vis. Sci. (Suppl.). Abstract #5347
- McGahan, M.C., S. Nagar, M. Goralska, L. Fleisher, J. Harned. 2012. Hypoxia regulates iron influx and efflux in retinal pigmented epithelial cells. Presented at XX International Society for Eye Research meeting, Berlin, Germany, July 2012.
- M. Goralska, L.N. Fleisher, M.C. McGahan. 2012. Hypoxia differentially affects expression of H- and L- ferritin chains in cultured lens epithelial cells. Presented at XX International Society for Eye Research meeting, Berlin, Germany, July 2012.
- McGahan, M.C., Nagar, S., Lall, M.M. 2013. Hypoxia affects polarized secretion of amyloid precursor protein from retinal pigmented epithelial cells. Invest. Ophthalmol. Vis. Sci. Abstract #6352. Presented at the ARVO meeting in Seattle, WA.
GeneticsRegulation of Fe metabolism in the eye, the involvement of Fe in cataract formation, mechanisms underlying post-surgical regrowth of lens tissue, uveitis, retinal physiology & pathology.
CURRENT RESEARCH - studies of iron metabolism in the eye
Alterations in cellular iron metabolism and storage in the lens and retinal pigmented epithelial cells result in significant changes in the size of the labile iron pool with concomitant physiological changes in glutamate and glutathione production and secretion, the activity of HIF-, the potential for pathophysioligcal changes and decreased ability to resist oxidative stress.
Cataract is a significant health and economic problem worldwide. In the United States and in other developed countries this is primarily an economic issue since surgery is readily available and is such an effective treatment. However, this is a multi-billion dollar expense, making up 12% of the entire Medicare Budget. In addition, there are some significant side-effects to cataract surgery. In developing countries, cataracts are the leading cause of blindness. Oxidative damage has been implicated as a causative factor in cataract formation and iron-catalyzed free radical reactions are responsible for virtually all oxidative tissue damage. Significantly, the level of iron is increased in older and in cataractous lenses. In addition to catalyzing oxidative damage and serving as an essential component of key enzymes, new roles for iron in cellular physiology are emerging. For example, we have made the novel observation that iron regulates glutamate production and the concentration of the powerful intracellular reducing agent, glutathione (GSH). Furthermore, others have shown that iron regulates the availability of the transcription factor, hypoxia inducible factor (HIF-1α). HIF-1α exerts significant effects on iron metabolism by controlling transcription of key proteins such as heme oxygenase, transferrin, transferrin receptor and ceruloplasmin (Cp). All cells carefully control iron uptake, utilization and storage. Most intracellular iron is safely stored in ferritin or incorporated into iron-dependent enzymes. However, there is a pool of chelatable iron in cells that is called the labile iron pool (LIP) that is thought to be a central transit pool from which iron is moved to sites of storage, utilization or removal from the cells and as such has been proposed to regulate iron-dependent intracellular reactions. The LIP is the likely source of iron for catalyzing free radical reactions. Little is known about regulation of the LIP, but it is possible to experimentally alter its size which we hypothesize will cause significant downstream effects (Fig. 1) the ubiquitous iron storage protein, ferritin, safely sequesters large quantities of iron, thus limiting the size of the LIP. Ferritin is made up of 24 subunits of two types, heavy (H) and light (L) that are present in tissue-specific ratios. Alteration of this ratio changes iron storage and the size of the LIP. Other factors which alter the size of the LIP include iron overload, iron depletion and chelation and treatment with Cp and transferrin.
labile iron pool
Our data have shown that:
- H- and L-chain ferritin composition in LEC changes with age and the structure of both chains is strikingly different from ferritin in the fiber mass.
- Altering the H:L ratio by overexpression of each chain or siRNA treatment changes iron metabolism and glutamate production.
- Iron controls the production of glutamate and the activity of the glutamate/cystine antiporter (Xc-). Increased glutamate antiporter activity increases cystine uptake.
- Cp increases the size of the LIP and increases glutamate secretion.
- HIF-1α and one of its targets, vascular endothelial growth factor (VEGF), are present in LEC and their availability is regulated by iron.
- Iron chelation and inhibition of aconitase-driven glutamate production decreases cystine uptake and GSH levels.
Fe regulates glutamate production including retinal pigment epithelial cellsDysregulation of iron metabolism has been strongly implicated in the progression of both neurological and retinal diseases, but little is known about the specific metabolic disturbances which underlie these processes. Iron is central to cellular metabolism and recent findings in our laboratory indicate new roles for this trace element which are critically relevant to retinal function (see Fig. 1). We have demonstrated that iron regulates glutamate production and secretion in a number of different cell types including retinal pigment epithelial cells (RPE). This is important to the retina for two reasons, first glutamate is an important neurotransmitter which can be excitotoxic and second, glutamate secretion by an antiporter provides cysteine for intracellular production of the powerful antioxidant, glutathione (GSH). Others have found that iron regulates the activity of the transcription factor, hypoxia inducible factor-1 (HIF-1). More than 60 proteins are regulated by HIF-1. We have convincing preliminary data indicating that iron regulates HIF-1, the downstream production of vascular endothelial growth factor (VEGF) and other iron regulatory proteins in RPE cells.
NIH Grant Support
- 1983-1986: NIH New Investigator Award EY-04900-01,2,3. Trace element dynamics in the vertebrate eye. (1/83-3/86; $149,730)
- 1986-1989: NIH grant EY-04900-04,5,6. Trace element dynamics in the vertebrate eye. (4/86-6/89; $348,226)
- 1989-1992: NIH grant EY-04900-7,8,9. Trace element dynamics in the vertebrate eye. (7/89-6/92; $467,074)
- 1992-1997: NIH grant EY-04900-10-14. Trace element dynamics in the vertebrate eye. (7/92-6/97; $1,031,541) Dr. M. Nasisse, Co-investigator.
- 1997-2001: NIH grant EY-04900-15-18. Trace element dynamics in the vertebrate eye. (7/97-6/01; $1,195,036)
- 2001-2006: NIH grant EY-04900-19-23. Trace element dynamics in the vertebrate eye. (7/01-6/06; $1,648,125)
- 2006-2011: NIH grant EY-04900-24-28. Trace element dynamics in the vertebrate eye (7/06-6/11; $1,272,670)
- 2011-2015: NIH grant EY-04900-29-32. Trace element dynamics in the vertebrate eye (8/11-7/15; $1,478,000)
- Hydrogen peroxide and ERK1/2 pathway regulate ferritin levels in retinal pigmented and lens epithelial cellsLall, M.M., J. Harned, M.C. McGahan | Mol. Vis. 19:2106-2112 | 2013
- Source-dependent subcellular distribution of iron in lens epithelial cells cultured in normoxic and hypoxic conditionsGoralska, M., S. Nagar, L.N. Fleisher, P. Mzyk, M.C. McGahan | Invest. Ophthalmol. Vis. Sci. In Press
- Ceruloplasmin alters intracellular iron regulated proteins and pathways: ferritin, transferrin receptor, glutamate and hypoxia-inducible factor-1αHarned, J., J. Ferrell, S. Nagar, M. Goralska, L.N. Fleisher, M.C. McGahan | Exp. Eye Res. 2012 Apr;97(1):90-7
- Altered ferritin subunit composition changes iron metabolism in lens epithelial cells with downstream effects on glutathione levels and vascular endothelial growth factor secretionHarned, J., J.B. Ferrell, M.M. Lall, L.N. Fleisher, S. Nagar, M. Goralska, M.C. McGahan | Invest. Ophthalmol. Vis. Sci. 51:4437-46 | 2010
- Changes in ferritin H- and L-chains in canine lenses with age-related nuclear cataract.Goralska, M., S. Nagar, C.M. Colitz, L.N. Fleisher, M.C. McGahan | Invest. Ophthalmol. Vis. Sci. 50:305-310 | Cover Article | 2009
- Iron metabolism in the eye: A reviewM. Goralska, J. Ferrell, J. Harned, M. Lall, S. Nagar, L.N. Fleisher, M.C. McGahan | Experimental Eye Research 88 (2009) 204-215
- Iron regulates L-cystine uptake and glutathione levels in lens epithelial and retinal pigment epithelial cells by its effect on cytosolic aconitaseLall, M., J. Ferrell, S. Nagar, M.C. McGahan | Invest. Opthalmol. Vis. Sci. 49:310-319 | Cover Article | 2008
- Ferritin H- and L-chains in fiber cells from canine and human lenses of different agesGoralska, M., L.N. Fleisher, M.C. McGahan | Invest. Ophthalmol. Vis. Sci. 48(9):3968-75 | 2007
- Lens epithelial cells synthesize and secrete ceruloplasmin: effects of ceruloplasmin and transferrin on iron efflux and intracellular iron dynamicsHarned, J., L.N. Fleisher and M.C. McGahan | Exp. Eye Res. 83(4):721-7. Epub | June 2006
- Iron alters glutamate secretion by regulating cytosolic aconitase activity McGahan, M.C., J. Harned, M. Mukunnemkeril, M. Goralska, L.N. Fleisher, J. Ferrell | Am. J. Physiol 288:C1117-C1124 | 2005
- Differential degradation of ferritin H- and L- chains: accumulation of L-chain rich ferritin in lens epithelial cellsGoralska, M., S. Nagar, L.N. Fleisher and M.C. McGahan | Invest. Ophthalmol. Vis. Sci. 46: 3521-3529 | Cover article | 2005
- Alpha lipoic acid changes Fe uptake and storage in lens epithelial cells Goralska, M., R. Dackor, B.L. Holley, M.C. McGahan | Exp. Eye Res. 76(2):241-8 | 2003
- The effect of UVB irradiation on ferritin subunit synthesis, ferritin assembly and Fe metabolism in cultured canine lens epithelial cellsGoralska, M., B.L. Holley and M.C.McGahan | J. Biol. Chem. 278:42920-42926 | 2003
Chris McGahan Named as Member of New Research Leadership AcademyThe newly created academy will promote a culture of research leadership at NC State and operate as the faculty-driven epicenter for the development and implementation of...
CVM Professor of Pharmacology Named One of NC State University's 125 Transformational Women
Dr. Christine McGahan, College of Veterinary Medicine professor of pharmacology, has been named by the Council on the Status of Women at North Carolina State University as one of the NC State’s 125 Transformational Women. Part of the university’s 125th anniversary activities, the honor celebrates the contributions and accomplishments of NC State women since 1887.
Dr. McGahan Named ARVO Fellow
Dr. Christine McGahan, head of the Department of Molecular Biomedical Sciences at the College of Veterinary Medicine, has been approved for the honor of “Gold Fellow” in the Association for Research in Vision and Ophthalmology Fellows Class of 2010. The title of Gold Fellow is an honor that recognizes association (ARVO) members for their individual