Bio

Academic Appointments


Honors & Awards


  • Ruth L. Kirschstein National Research Service Award Individual Postdoctoral Fellowship (F32), NEI (2015-2018)

Professional Education


  • Postdoctoral Fellow, Stanford University School of Medicine (2019)
  • Postdoctoral Scholar, University of California San Diego (2015)
  • PhD, University of Maryland Baltimore County (2014)
  • MS, University of Maryland Baltimore County (2007)
  • BS, Towson University (2006)

Publications

All Publications


  • Opposing Effects of Growth and Differentiation Factors in Cell-Fate Specification. Current biology : CB Chang, K. C., Sun, C., Cameron, E. G., Madaan, A., Wu, S., Xia, X., Zhang, X., Tenerelli, K., Nahmou, M., Knasel, C. M., Russano, K. R., Hertz, J., Goldberg, J. L. 2019

    Abstract

    Following ocular trauma or in diseases such as glaucoma, irreversible vision loss is due to the death of retinal ganglion cell (RGC) neurons. Although strategies to replace these lost cells include stem cell replacement therapy, few differentiated stem cells turn into RGC-like neurons. Understanding the regulatory mechanisms of RGC differentiation in vivo may improve outcomes of cell transplantation by directing the fate of undifferentiated cells toward mature RGCs. Here, we report a new mechanism by which growth and differentiation factor-15 (GDF-15), a ligand in the transforming growth factor-beta (TGF-?) superfamily, strongly promotes RGC differentiation in the developing retina in vivo in rodent retinal progenitor cells (RPCs) and in human embryonic stem cells (hESCs). This effect is in direct contrast to the closely related ligand GDF-11, which suppresses RGC-fate specification. We find these opposing effects are due in part to GDF-15's ability to specifically suppress Smad-2, but not Smad-1, signaling induced by GDF-11, which can be recapitulated by pharmacologic or genetic blockade of Smad-2 in vivo to increase RGC specification. No other retinal cell types were affected by GDF-11 knockout, but a slight reduction in photoreceptor cells was observed by GDF-15 knockout in the developing retina in vivo. These data define a novel regulatory mechanism of GDFs' opposing effects and their relevance in RGC differentiation and suggest a potential approach for advancing ESC-to-RGC cell-based replacement therapies.

    View details for DOI 10.1016/j.cub.2019.05.011

    View details for PubMedID 31155355

  • Regulation of Neuronal Survival and Axon Growth by a Perinuclear cAMP Compartment. The Journal of neuroscience : the official journal of the Society for Neuroscience Boczek, T., Cameron, E. G., Yu, W., Xia, X., Shah, S. H., Castillo Chabeco, B., Galvao, J., Nahmou, M., Li, J., Thakur, H., Goldberg, J. L., Kapiloff, M. S. 2019

    Abstract

    Cyclic-AMP (cAMP) signaling is known to be critical in neuronal survival and axon growth. Increasingly the subcellular compartmentation of cAMP signaling has been appreciated, but outside of dendritic synaptic regulation, few cAMP compartments have been defined in terms of molecular composition or function in neurons. Specificity in cAMP signaling is conferred in large part by A-kinase anchoring proteins (AKAPs) that localize protein kinase A (PKA) and other signaling enzymes to discrete intracellular compartments. We now reveal that cAMP signaling within a perinuclear neuronal compartment organized by the large multivalent scaffold protein mAKAP? promotes neuronal survival and axon growth. mAKAP? signalosome function is explored using new molecular tools designed to specifically alter local cAMP levels as studied by live cell FRET imaging. In addition, enhancement of mAKAP?-associated cAMP signaling by isoform-specific displacement of bound phosphodiesterase is demonstrated to increase retinal ganglion cell survival in vivo in mice of both sexes following optic nerve crush injury. These findings define a novel neuronal compartment that confers cAMP regulation of neuroprotection and axon growth and that may be therapeutically targeted in disease.SIGNIFICANCE STATEMENTcAMP is a second messenger responsible for the regulation of diverse cellular processes including neuronal neurite extension and survival following injury. Signal transduction by cAMP is highly compartmentalized in large part due to the formation of discrete, localized multimolecular signaling complexes by A-kinase anchoring proteins. Although the concept of cAMP compartmentation is well-established, the function and identity of these compartments remain poorly understood in neurons. In this study, we provide evidence for a neuronal perinuclear cAMP compartment organized by the scaffold protein mAKAP? that is necessary and sufficient for the induction of neurite outgrowth in vitro and for the survival of retinal ganglion cells in vivo following optic nerve injury.

    View details for PubMedID 31097623

  • Intracellular compartmentation of cAMP promotes neuroprotection and regeneration of CNS neurons. Neural regeneration research Cameron, E. G., Kapiloff, M. S. 2017; 12 (2): 201?2

    View details for PubMedID 28400794

    View details for PubMedCentralID PMC5361496

  • NEUROREGENERATION. Promoting CNS repair. Science Cameron, E. G., Goldberg, J. L. 2016; 353 (6294): 30-31

    View details for DOI 10.1126/science.aag3327

    View details for PubMedID 27365439

  • Muscle A-Kinase Anchoring Protein-a is an Injury-Specific Signaling Scaffold Required for Neurotrophic- and Cyclic Adenosine Monophosphate-Mediated Survival. EBioMedicine Wang, Y., Cameron, E. G., Li, J., Stiles, T. L., Kritzer, M. D., Lodhavia, R., Hertz, J., Nguyen, T., Kapiloff, M. S., Goldberg, J. L. 2015; 2 (12): 1880-1887

    Abstract

    Neurotrophic factor and cAMP-dependent signaling promote the survival and neurite outgrowth of retinal ganglion cells (RGCs) after injury. However, the mechanisms conferring neuroprotection and neuroregeneration downstream to these signals are unclear. We now reveal that the scaffold protein muscle A-kinase anchoring protein-? (mAKAP?) is required for the survival and axon growth of cultured primary RGCs. Although genetic deletion of mAKAP? early in prenatal RGC development did not affect RGC survival into adulthood, nor promoted the death of RGCs in the uninjured adult retina, loss of mAKAP? in the adult increased RGC death after optic nerve crush. Importantly, mAKAP? was required for the neuroprotective effects of brain-derived neurotrophic factor and cyclic adenosine-monophosphate (cAMP) after injury. These results identify mAKAP? as a scaffold for signaling in the stressed neuron that is required for RGC neuroprotection after optic nerve injury.

    View details for DOI 10.1016/j.ebiom.2015.10.025

    View details for PubMedID 26844267

  • beta-Arrestin-Dependent Deactivation of Mouse Melanopsin PLOS ONE Cameron, E. G., Robinson, P. R. 2014; 9 (11)

    Abstract

    In mammals, the expression of the unusual visual pigment, melanopsin, is restricted to a small subset of intrinsically photosensitive retinal ganglion cells (ipRGCs), whose signaling regulate numerous non-visual functions including sleep, circadian photoentrainment and pupillary constriction. IpRGCs exhibit attenuated electrical responses following sequential and prolonged light exposures indicative of an adaptational response. The molecular mechanisms underlying deactivation and adaptation in ipRGCs however, have yet to be fully elucidated. The role of melanopsin phosphorylation and ?-arrestin binding in this adaptive process is suggested by the phosphorylation-dependent reduction of melanopsin signaling in vitro and the ubiquitous expression of ?-arrestin in the retina. These observations, along with the conspicuous absence of visual arrestin in ipRGCs, suggest that a ?-arrestin terminates melanopsin signaling. Here, we describe a light- and phosphorylation- dependent reduction in melanopsin signaling mediated by both ?-arrestin 1 and ?-arrestin 2. Using an in vitro calcium imaging assay, we demonstrate that increasing the cellular concentration of ?-arrestin 1 and ?-arrestin 2 significantly increases the rate of deactivation of light-activated melanopsin in HEK293 cells. Furthermore, we show that this response is dependent on melanopsin carboxyl-tail phosphorylation. Crosslinking and co-immunoprecipitation experiments confirm ?-arrestin 1 and ?-arrestin 2 bind to melanopsin in a light- and phosphorylation- dependent manner. These data are further supported by proximity ligation assays (PLA), which demonstrate a melanopsin/?-arrestin interaction in HEK293 cells and ipRGCs. Together, these results suggest that melanopsin signaling is terminated in a light- and phosphorylation-dependent manner through the binding of a ?-arrestin within the retina.

    View details for DOI 10.1371/journal.pone.0113138

    View details for Web of Science ID 000345158700116

    View details for PubMedID 25401926

  • Characterization of visual pigments, oil droplets, lens and cornea in the whooping crane Grus americana JOURNAL OF EXPERIMENTAL BIOLOGY Porter, M. L., Kingston, A. C., McCready, R., Cameron, E. G., Hofmann, C. M., Suarez, L., Olsen, G. H., Cronin, T. W., Robinson, P. R. 2014; 217 (21): 3883-3890

    Abstract

    Vision has been investigated in many species of birds, but few studies have considered the visual systems of large birds and the particular implications of large eyes and long-life spans on visual system capabilities. To address these issues we investigated the visual system of the whooping crane Grus americana (Gruiformes, Gruidae), which is one of only two North American crane species. It is a large, long-lived bird in which UV sensitivity might be reduced by chromatic aberration and entrance of UV radiation into the eye could be detrimental to retinal tissues. To investigate the whooping crane visual system we used microspectrophotometry to determine the absorbance spectra of retinal oil droplets and to investigate whether the ocular media (i.e. the lens and cornea) absorb UV radiation. In vitro expression and reconstitution was used to determine the absorbance spectra of rod and cone visual pigments. The rod visual pigments had wavelengths of peak absorbance (?max) at 500 nm, whereas the cone visual pigment ?max values were determined to be 404 nm (SWS1), 450 nm (SWS2), 499 nm (RH2) and 561 nm (LWS), similar to other characterized bird visual pigment absorbance values. The oil droplet cut-off wavelength (?cut) values similarly fell within ranges recorded in other avian species: 576 nm (R-type), 522 nm (Y-type), 506 nm (P-type) and 448 nm (C-type). We confirm that G. americana has a violet-sensitive visual system; however, as a consequence of the ?max of the SWS1 visual pigment (404 nm), it might also have some UV sensitivity.

    View details for DOI 10.1242/jeb.108456

    View details for Web of Science ID 000344866300022

    View details for PubMedID 25267845

  • Identification of Critical Phosphorylation Sites on the Carboxy Tail of Melanopsin BIOCHEMISTRY Blasic, J. R., Matos-Cruz, V., Ujla, D., Cameron, E. G., Hattar, S., Halpern, M. E., Robinson, P. R. 2014; 53 (16): 2644-2649

    Abstract

    Light-activated opsins undergo carboxy-terminal phosphorylation, which contributes to the deactivation of their photoresponse. The photopigment melanopsin possesses an unusually long carboxy tail containing 37 serine and threonine sites that are potential sites for phosphorylation by a G-protein dependent kinase (GRK). Here, we show that a small cluster of six to seven sites is sufficient for deactivation of light-activated mouse melanopsin. Surprisingly, these sites are distinct from those that regulate deactivation of rhodopsin. In zebrafish, there are five different melanopsin genes that encode proteins with distinct carboxy-terminal domains. Naturally occurring changes in the same cluster of phosphorylatable amino acids provides diversity in the deactivation kinetics of the zebrafish proteins. These results suggest that variation in phosphorylation sites provides flexibility in the duration and kinetics of melanopsin-mediated light responses.

    View details for DOI 10.1021/bi401724r

    View details for Web of Science ID 000335297200009

    View details for PubMedID 24678795

  • Shedding new light on opsin evolution PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES Porter, M. L., Blasic, J. R., Bok, M. J., Cameron, E. G., Pringle, T., Cronin, T. W., Robinson, P. R. 2012; 279 (1726): 3-14

    Abstract

    Opsin proteins are essential molecules in mediating the ability of animals to detect and use light for diverse biological functions. Therefore, understanding the evolutionary history of opsins is key to understanding the evolution of light detection and photoreception in animals. As genomic data have appeared and rapidly expanded in quantity, it has become possible to analyse opsins that functionally and histologically are less well characterized, and thus to examine opsin evolution strictly from a genetic perspective. We have incorporated these new data into a large-scale, genome-based analysis of opsin evolution. We use an extensive phylogeny of currently known opsin sequence diversity as a foundation for examining the evolutionary distributions of key functional features within the opsin clade. This new analysis illustrates the lability of opsin protein-expression patterns, site-specific functionality (i.e. counterion position) and G-protein binding interactions. Further, it demonstrates the limitations of current model organisms, and highlights the need for further characterization of many of the opsin sequence groups with unknown function.

    View details for DOI 10.1098/rspb.2011.1819

    View details for Web of Science ID 000297674300002

    View details for PubMedID 22012981

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