Literature DB >> 30451216

Ultrahigh Resolution Mouse Optical Coherence Tomography to Aid Intraocular Injection in Retinal Gene Therapy Research.

Mark C Butler1, Jack M Sullivan2.   

Abstract

HR-SD-OCT is utilized to monitor the progression of photoreceptor degeneration in live mouse models, assess the delivery of therapeutic agents into the subretinal space, and to evaluate toxicity and efficacy in vivo. HR-SD-OCT uses near infrared light (800-880 nm) and has optics specifically designed for the unique optics of the mouse eye with sub-2-micron axial resolution. Transgenic mouse models of outer retinal (photoreceptor) degeneration and controls were imaged to assess the disease progression. Pulled glass microneedles were used to deliver sub retinal injections of adeno-associated virus (AAV) or nanoparticles (NP) via a trans-scleral and trans-choroidal approach. Careful positioning of the needle into the subretinal space was required prior to a calibrated pressure injection, which delivers fluid into the sub retinal space. Real time subretinal surgery was conducted on our retinal imaging system (RIS). HR-SD-OCT demonstrated progressive uniform retinal degeneration due to expression of a toxic mutant human mutant rhodopsin (P347S) (RHOP347S) transgene in mice. HR-SD-OCT allows rigorous quantification of all the retinal layers. Outer nuclear layer (ONL) thickness and photoreceptor outer segment length (OSL) measurements correlate with photoreceptor vitality, degeneration, or rescue. The RIS delivery system allows real-time visualization of subretinal injections in neonatal (~P10-14) or adult mice, and HR-SD-OCT immediately determines success of delivery and maps areal extent. HR-SD-OCT is a powerful tool that can evaluate the success of subretinal surgery in mice, in addition to measuring vitality of photoreceptors in vivo. HR-SD-OCT can also be used to identify uniform animal cohorts to evaluate the extent of retinal degeneration, toxicity, and therapeutic rescue in preclinical gene therapy research studies.

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Mesh:

Year:  2018        PMID: 30451216      PMCID: PMC7027489          DOI: 10.3791/55894

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  33 in total

Review 1.  Bottlenecks in development of retinal therapeutic post-transcriptional gene silencing agents.

Authors:  Jack M Sullivan; Edwin H Yau; R Thomas Taggart; Mark C Butler; Tiffany A Kolniak
Journal:  Vision Res       Date:  2007-10-31       Impact factor: 1.886

2.  Subretinal gene therapy of mice with Bardet-Biedl syndrome type 1.

Authors:  Seongjin Seo; Robert F Mullins; Alina V Dumitrescu; Sajag Bhattarai; Daniel Gratie; Kai Wang; Edwin M Stone; Val Sheffield; Arlene V Drack
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-09-11       Impact factor: 4.799

3.  RD3 gene delivery restores guanylate cyclase localization and rescues photoreceptors in the Rd3 mouse model of Leber congenital amaurosis 12.

Authors:  Laurie L Molday; Hidayat Djajadi; Paul Yan; Lukasz Szczygiel; Sanford L Boye; Vince A Chiodo; Kevin Gregory-Evans; Marinko V Sarunic; William W Hauswirth; Robert S Molday
Journal:  Hum Mol Genet       Date:  2013-06-04       Impact factor: 6.150

4.  Rapid, cell-based toxicity screen of potentially therapeutic post-transcriptional gene silencing agents.

Authors:  Tiffany A Kolniak; Jack M Sullivan
Journal:  Exp Eye Res       Date:  2011-01-21       Impact factor: 3.467

5.  In vivo three-dimensional high-resolution imaging of rodent retina with spectral-domain optical coherence tomography.

Authors:  Marco Ruggeri; Hassan Wehbe; Shuliang Jiao; Giovanni Gregori; Maria E Jockovich; Abigail Hackam; Yuanli Duan; Carmen A Puliafito
Journal:  Invest Ophthalmol Vis Sci       Date:  2007-04       Impact factor: 4.799

6.  Retinopathy induced in mice by targeted disruption of the rhodopsin gene.

Authors:  M M Humphries; D Rancourt; G J Farrar; P Kenna; M Hazel; R A Bush; P A Sieving; D M Sheils; N McNally; P Creighton; A Erven; A Boros; K Gulya; M R Capecchi; P Humphries
Journal:  Nat Genet       Date:  1997-02       Impact factor: 38.330

7.  Targeting Caspase-12 to Preserve Vision in Mice With Inherited Retinal Degeneration.

Authors:  Yogesh Bhootada; Shreyasi Choudhury; Clark Gully; Marina Gorbatyuk
Journal:  Invest Ophthalmol Vis Sci       Date:  2015-07       Impact factor: 4.799

8.  Trans-Corneal Subretinal Injection in Mice and Its Effect on the Function and Morphology of the Retina.

Authors:  Yan Qi; Xufeng Dai; Hua Zhang; Ying He; Yangyang Zhang; Juanjuan Han; Ping Zhu; Yuxin Zhang; Qinxiang Zheng; Xia Li; Chen Zhao; Jijing Pang
Journal:  PLoS One       Date:  2015-08-28       Impact factor: 3.240

9.  Retinal thickness measurement obtained with spectral domain optical coherence tomography assisted optical biopsy accurately correlates with ex vivo histology.

Authors:  Lee R Ferguson; Sandeep Grover; James M Dominguez; Sankarathi Balaiya; Kakarla V Chalam
Journal:  PLoS One       Date:  2014-10-31       Impact factor: 3.240

Review 10.  RNA interference gene therapy in dominant retinitis pigmentosa and cone-rod dystrophy mouse models caused by GCAP1 mutations.

Authors:  Li Jiang; Jeanne M Frederick; Wolfgang Baehr
Journal:  Front Mol Neurosci       Date:  2014-04-07       Impact factor: 5.639

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  1 in total

Review 1.  Subretinal Injection Techniques for Retinal Disease: A Review.

Authors:  Cristina Irigoyen; Asier Amenabar Alonso; Jorge Sanchez-Molina; María Rodríguez-Hidalgo; Araceli Lara-López; Javier Ruiz-Ederra
Journal:  J Clin Med       Date:  2022-08-12       Impact factor: 4.964

  1 in total

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