Section for Translational Research on Retinal and Macular Degeneration

National Institute on Deafness and Other Communication Disorders*
National Institutes of Health
Louis B. Stokes Laboratories, Building 50, Room 4339
50 South Drive
Bethesda, Maryland 20892-8021
Phone: (301) 451-9772
Fax: (301) 480-4799
E-mail: sievingpa@nei.nih.gov

Principal Investigator: Paul A. Sieving, M.D., Ph.D.

On this page:

Overview

Dr. Sieving’s research program focuses on structural and functional studies of photoreceptors, neurons and glia in the reinta of animal models and humans, in health and disease. The laboratory (STRRMD) is structured to include a broad range of expertise: retinal electrophysiology, genetic models of human blinding diseases, retinal cell biology and biochemistry, molecular biology, and gene therapy. A major impetus of STRRMD research is translational, whereby studies in rodent models of human genetic blinding diseases provide clues for therapeutic intervention. Dr. Sieving leads a highly dynamic research team and has established a unique and strong research program that is well poised to make breakthroughs to bring novel therapies to retinal degeneration patients.

This laboratory recently conducted the first human trial of ciliary neurotrophic factor (CNTF) as possible treatment for human hereditary retinal degenerative diseases, known principally as retinitis pigmentosa [Sieving, 2006]. This phase-1 trial of intraocular implants that release CNTF evolved as a translational project from laboratory work conducted by Dr. Sieving and Dr. Ronald Bush to explore small molecules and proteins that provide narrow protection for RP-class ocular diseases [Bush, 2004].

A major current laboratory translational focus is on gene therapy for X-linked retinoschisis (XLRS). The laboratory is completing pre-clinical studies to show efficacy of gene replacement therapy with a gene-knockout XLRS mouse model. These data, along with gene vector toxicity results, will be presented to FDA in preparation to mounting a human gene therapy trial for XLRS.

Back to Top

Research Projects

  1. RCS Rodent Models of Retinal Degeneration
  2. Staining of Retinal Cells for Kir 2.1 Antibody (red)
    Figure 1: Using antibodies to probe the origin of electroretinogram (ERG) signals in a rat model of retinitis pigmentosa. Antibodies to Kir 2.1 potassium channels administered to the eye of an RCS rat before recording the ERG reduced the signal coming from the inner retina, but non-specific immunoglobulin (IgG) did not. The Kir 2.1 antibody (stained red) administered in vivo binds to specific inner retinal cells in the same location as when the antibody is applied to retinal sections in vitro. IgG staining is diffuse and non-specific.

    The STRRMD utilizes the electroretinogram (ERG) to dissect complex retinal processes in health and disease. The laboratory has characterized a novel and prominent corneal-negative ERG response in the Royal College of Surgeons (RCS) rat, a retinal degeneration model with a mutation in the Mertk gene. The retinal cellular origin of this response, named “negative photopic response” (NPR), was dissected by applying agents that disrupt synaptic signaling between specific cell types to identify the contributing neurons. This study implicated the activity of amacrine cells in the generation of the NPR [Machida, 2008]. The lab has also determined the role of K+ channels in the RCS-NPR response by developing a novel technique using antibodies against K+ channels coupled to a short Pep-1 peptide that facilitates delivery across the cell membrane and into the cell. In vivo functional data has demonstrated that Kir2.1 and Kir4.1 channels contribute to the generation of the RCS-NPR component. This was shown using electroretinogram recordings and by single cell patch clamp electrophysiology. The STRRMD has developed neurotrophic factor (LEDGF) gene therapy in the RCS rat using adeno-associated virus (AAV) as the delivery vector. This gene therapy strategy has restored retinal signaling and normalized the ERG response. Similar work could be extended to human patients.

    Back to Top

  3. Rac1 Involvement in ROS Morphogenesis, Homeostasis, and Rod Degeneration
  4. Rac1 Involvement in ROS Morphogenesis, Homeostasis, and Rod Degeneration
    Figure 2: Depleting Rac1 in mouse photoreceptors protects them from damage by light. Staining for Rac1 (brown) in retinas of mice in which the gene in photoreceptors has been knocked down shows that less Rac1 is present in the photoreceptors than in litter mates in which the gene is normal (wild type). When exposed to bright light, the damage and loss of photoreceptors is less in mice with depletion of Rac1.

    Another thread to the research in the laboratory is related to the investigation of the protein Rac1 in rod photoreceptor outer-segment (OS) turnover and homeostasis. In animal models that fail to express rhodopsin, there is a failure of rod OS to develop, leading to rod-cell degeneration. In Drosophila mutants lacking opsin expression, photoreceptor rhabdomeres fail to develop normally but can be rescued by constitutively active Rac1. This suggests that rhodopsin controls the development of rod OS via Rac1 activation. The STRRMD is investigating whether Rac1 plays a similar role in the mouse, and if so, whether the manipulation of Rac1 expression provides a means to rescue photoreceptors in retinal degeneration associated with rhodopsin mutations. Dr. Sieving and his team have created and characterized a Rac1 rod conditional knockdown mouse (Rac1-CKO) and have demonstrated that Rac1 depletion in rods reduced light-induced photoreceptor degeneration [Haruta, 2009]. Recent data show that the molecular pathways downstream of Rac1 might contribute to the neuroprotective response via AP1 and STAT3, and that decreased activation of Rac1 and NADPH-oxidase function contribute to photoreceptor survival following light-induced photoreceptor damage in Rac1-CKO mice.

    Back to Top

  5. X-linked Retinoschisis (XLRS) Disease

X-linked Retinoschisis (XLRS) Disease
Figure 3: This figure demonstrated that the retina structure restoration after gene therapy. Left panel showed OCT images (Optical Coherence Tomography) taken from mouse retina; right panel showed retinoschisin protein expressing in mouse retina. a. Images were taken from wild type mouse. b. and c. Images were taken from RS1-null mouse: b. gene therapy treated eye of RS1-null mouse, there was no cavities and split in the inner nuclear layer (INL), and the structure of retina was well organized, but the outer nuclear layer (ONL) was still thinner than the retina of wild type mouse; c. Untreated eye of RS1-null mouse, there were severe cavities in the inner nuclear layer (INL).

Dr. Sieving and his group are investigating the molecular pathology of XLRS disease and are working toward developing gene therapy for this disorder. XLRS is the most common from of macular dystrophy in young males; and there is no effective treatment. All affected males have macular changes, and the majority also present changes in the peripheral retina. The natural history is a slow deterioration in central retinal function. XLRS does not cause outright complete blindness unless there are secondary complications such as retinal detachment or vitreous hemorrhage. The causative gene (retinoschisin, RS1) was identified in 1997, and molecular diagnosis and genetic testing are now available through an affiliated lab. XLRS mutations have been correlated with the disease phenotype. A functional hallmark of XLRS is an electronegative ERG with a markedly reduced b-wave.

Progress in this research includes creation of RS1 null mice [Zeng, 2004] and the characterization of the long-term history of retinal degeneration [Kjellstrom 2007]. They identified synaptic pathology in RS1 knockout mice—which should provide novel insights into the mechanisms underlying RS1 defects [Takada, 2008]. Study showed the effect of retinoschisin deficit during retinal detachment (in collaboration with Dr. Steve Fisher: Luna, 2009); the characterization of a recombinant viral vector (AAV8-RS1promoterhumanRS1 gene) in preparation for clinical gene therapy; and demonstrated structural and functional rescue of photoreceptors by intravitreal RS1 gene transfer in the XLRS mice. Collectively, these studies form the basis for planning translational work toward a phase-1 human clinical trial by intravitreal administration of the human XLRS gene. An exciting part of the research relates to the demonstration that gene therapy can restore normal ERG responses in the mouse model. Although initial work used subretinal injections to deliver the vector, the Sieving lab has now successfully demonstrated that intravitreal injections using AAV2 vectors are equally effective. Moreover after transfection, high levels of retinoschisin protein expression could be demonstrated in photoreceptors—a surprising finding since previous publications, including Dr. Sieving’s own work, have shown that these vectors normally do not penetrate the outer retina in wild type animals. The demonstration that intravitreal administration of vector is effective in XLRS is likely to have major implications for the ease and safety of gene therapy for human ocular disease in the future. The Sieving laboratory has developed a human clinical trial protocol and has had preliminary discussions with the FDA regarding a phase-1 trial of gene replacement therapy.

Back to Top

Tools and Approaches

The laboratory works at multiple levels, from cultured cells to whole animal ocular physiology, biochemistry and molecular biology and genetics. Ronald Bush, Ph.D., is the principal staff scientist and directs the work using electroretinogram recordings and rhodopsin photochemistry for retinal functional study and structural analysis using morphometric techniques and immunohistochemistry. He has particular expertise and has published extensively on retinal light damage and photostasis in rats, models of rod photoreceptor degeneration and plasticity.

Back to Top

Personnel

Name Title E-mail
Paul A. Sieving, M.D., Ph.D. Section Chief sievingpa@nei.nih.gov
Ronald A. Bush, Ph.D. Staff Scientist bushr@nidcd.nih.gov
Yong Zeng, M.D. Biologist zengy@mail.nih.gov
Vijayasarathy Camasamudram, Ph.D. Biochemist camasamudramv@nidcd.nih.gov
Lucia Ziccardi, M.D. Visiting Fellow ziccardil@mail.nih.gov
Hongman Song, M.D., Ph.D. Visiting Fellow songh2@mial.nih.gov
Jinbo Li Histology Technician lijinb@nidcd.nih.gov
Zoe Gutterman IRTA Technician guttermanza@mail.nih.gov
Maria Santos Technician santosmm@nei.nih.gov

Back to Top

Selected Publications

  • KjellstrÖm S, Camasamudram C, Ponjavic V, Sieving PA, Andréasson S. Long-term 12 year follow-up of X-linked congenital retinoschisis. Ophthalmic Genet 31(3):114-25. (2010)
  • Kotova S, Vijayasarathy C, Dimitriadis EK, Ikonomou L, Jaffe H, Sieving PA. Retinoschisin (RS1) interacts with negatively charged lipid bilayers in the presence of Ca2+: an atomic force microscopy study. Biochemistry 49(33):7023-32. (2010)
  • Raz-Prag D, Grimes WN, Fariss RN, Vijayasarathy C, Campos MM, Bush RA, Diamond JS, Sieving PA. Probing potassium channel function in vivo by intracellular delivery of antibodies in a rat model of retinal neurodegeneration. PNAS 107(28):12710-5. (2010)
  • Sergeev YV, Caruso RC, Meltzer MR, Smaoui N, MacDonald IM, Sieving PA. Molecular modeling of retinoschisin with functional analysis of pathogenic mutations from human X-linked retinoschisis. Hum Mol Genet 19(7):1302-13. (2010)
  • Vijayasarathy C, Sui R, Zeng Y, Yang G, Xu F, Caruso RC, Lewis RA, Ziccardi L, Sieving PA. Molecular mechanisms leading to null-protein product from retinoschisin (RS1) signal-sequence mutants in X-linked retinoschisis (XLRS) disease. Hum Mut 31(11):1251-60.
  • Haruta M, Bush RA, Kjellstroma S, Vijayasarathya C, Zeng Y, Le Y-Z, Sieving PA. Depleting Rac1in mouse rod photoreceptors protects them from photo-oxidative stress without affecting their structure or function. PNAS 106(23):9397-402. (2009)
  • Luna G, Kjellstrom S, Verardo M, Lewis GP, Byun J, Sieving PA, Fisher SK. The effects of transient retinal detachment on cavity size and glial and neural remodeling in a mouse model of X-linked retinoschisis. IOVS 50(8):3977-84. (2009)
  • Park TK, Wu Z, Kjellstrom S, Zeng Y, Bush RA, Sieving PA, Colosi P. Intravitreal delivery of AAV8 retinoschisin results in cell type-specific gene expression and retinal rescue in the RS1-Ko mouse. Gene Therapy 16:916-26. (2009)
  • Raz-Prag D, Zeng Y, Sieving PA, Bush RA. Photoreceptor protection by adeno-associated virus-mediated LEDGF expression in the RCS rat model of retinal degeneration: probing the mechanism. IOVS 50(8):3897-906. (2009)
  • Vijayasarathy C, Ziccardi L, Zeng Y, Smaoui N, Caruso RC, Sieving PA. Null retinoschisin-protein expression from an RS1 c354del1-ins18 mutation causes progressive and severe XLRS in a cross-sectional family study. IOVS 50(11):5375-83. (2009)
  • Ahmed ZM, Kjellstrom S, Haywood-Watson RJ, Bush RA, Hampton LL, Battey JF, Riazuddin S, Frolenkov G, Sieving PA, Friedman TB. Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degeneration. Mol Vis 14:2227-36. (2008)
  • Machida S, Raz-Prag D, Fariss RN, Sieving PA, Bush RA. Photopic ERG negative response from amacrine cell signaling in RCS rat retinal degeneration. IOVS 49(1):442-52. (2008)
  • Takada Y, Vijayasarathy C, Zeng Y, Kjellstrom S, Bush RA, Sieving PA. Synaptic pathology in retino-schisis knockout (Rs1-/y) mouse retina and modification by rAAV-Rs1 gene delivery. IOVS 49(8):3677-86. (2008)
  • Vijayasarathy C, Takada Y, Zeng Y, Bush RA, Sieving PA. Organization and molecular interactions of retinoschisin in photoreceptors. Adv Exp Med Biol 613:291-7. (2008)
  • Khan NW, Wissinger B, Kohl S, Sieving PA. CNGB3 achromatopsia with progressive loss of residual cone function and impaired rod-mediated function. IOVS 48(8):3864-71. (2007)
  • Kjellstrom S, Bush RA, Zeng Y, Takada Y, Sieving PA. Retinoschisin gene therapy and natural history in the Rs1h-KO mouse: long-term rescue from retinal degeneration. IOVS 48(8): 3837-45. (2007)
  • MacDonald IM, Sauvé Y, Sieving PA. Preventing blindness in retinal disease: ciliary neurotrophic factor intraocular implants. Can J Ophthalmol 42(3):399-402. (2007)
  • Vijayasarathy C, Takada Y, Zeng Y, Bush RA, Sieving PA. Retinoschisin is a peripheral membrane protein with affinity for anionic phospholipids and affected by divalent cations. IOVS 48(3): 991-1000. (2007)
  • Woodruff ML, Olshevskaya EV, Savchenko AB, Peshenko IV, Barrett R, Bush RA, Sieving PA, Fain GL, Dizhoor AM. Constitutive excitation by Gly90Asp rhodopsin rescues rods from degeneration caused by elevated production of cGMP in the dark. J Neurosci 27(33):8805-15. (2007)
  • Zhang Q, Zulfiqar F, Xiao X, Riazuddin SA, Ahmad Z, Caruso R, MacDonald I, Sieving P, Riazuddin S, Hejtmancik JF. Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene. Hum Genet 122(3-4):293-9. (2007)
  • Haywood-Watson RJ 2nd, Ahmed ZM, Kjellstrom S, Bush RA, Takada Y, Hampton LL, Battey JF, Sieving PA, Friedman TB. Ames Waltzer deaf mice have reduced electroretinogram amplitudes and complex alternative splicing of Pcdh15 transcripts. IOVS 47(7):3074-84. (2006)
  • Raz-Prag D, Ayyagari R, Fariss RN, Mandal MN, Vasireddy V, Majchrzak S, Webber AL, Bush RA, Salem N Jr, Petrukhin K, Sieving PA. Haploinsufficiency is not the key mechanism of pathogenesis in a heterozygous Elovl4 knockout mouse model of STGD3 disease. IOVS 47(8):3603-11. (2006)
  • Riazuddin SA, Zulfiqar F, Zhang Q, Yao W, Li S, Jiao X, Shahzadi A, Amer M, Iqbal M, Hussnain T, Sieving PA, Riazuddin S, Hejtmancik JF. Mutations in the gene encoding the α-subunit of rod phosphodiesterase in consanguineous Pakistani families. Mol Vis 12:1283-91. (2006)
  • Sieving PA, Caruso RC, Tao W, Coleman HR, Thompson DJS, Fullmer KR, Bush RA. Ciliary neurotrophic factor (CNTF) for human retinal degeneration: phase-1 trial of CNTF delivered by encapsulated cell intraocular implants. PNAS (USA) 103(10):3896-3901. (2006)
  • Takada Y, Fariss RN, Müller M, Bush RA, Rushing EJ, Sieving PA. Retinoschisin expression and localization in rodent and human pineal and consequences of mouse RS1 gene knockout. Mol Vis 12:1108-16. (2006)
  • Vasireddy V, Jablonski MM, Mandal MN, Raz-Prag D, Wang XF, Nizol L, Iannaccone A, Musch DC, Bush RA, Salem N Jr, Sieving PA, Ayyagari R. Elovl4 5-bp-deletion knock-in mice develop progressive photoreceptor degeneration. IOVS 47(10):4558-68. (2006)
  • Vijayasaryathy C, Gawinowicz MA, Zeng Y, Takada Y, Bush RA, Sieving PA. Identification and characterization of two mature isoforms of retinoschisin in murine retina. Biochem Biophys Res Commun 349(1):99-105. (2006)
  • Wen R, Song Y, Kjellstrom S, Tanikawa A, Liu Y, Li Y, Zhao Y, Bush RA, Laties AM, Sieving PA. Regulation of rod phototransduction machinery by ciliary neurotrophic factor. J Neurosci 26(52):13523-30. (2006)
  • Bush RA, Lei B, Tao W, Raz D, Chan C, Cox TA, Santos-Muffley M, Sieving PA. Encapsulated cell-based intraocular delivery of ciliary neurotrophic factor in normal rabbit: dose-dependent effects on ERG and retinal histology. IOVS 45(7):2420-30.
  • Zeng Y, Takada Y, Kjellstrom S, Hiriyanna K, Tanikawa A, Wawrousek E, Smaoui N, Caruso R, Bush RA, Sieving PA. RS-1 gene delivery to an adult Rs1h knockout mouse model restores ERG b-wave with reversal of the electronegative waveform of X-linked retinoschisis. IOVS 45(9):3279-85.

Back to Top


*The Section for Translational Research on Retinal and Macular Degeneration (STRRMD), a laboratory engaged in eye and vision research at the National Institutes of Health (NIH), is administered by the Division of Intramural Research, National Institute on Deafness and Other Communication Disorders (DIR/NIDCD/NIH). For practical considerations of web browsing and research, the STRRMD appears here on the web pages of the Division of Intramural Research, National Eye Institute.