Literature DB >> 25896245

CNTF Gene Therapy Confers Lifelong Neuroprotection in a Mouse Model of Human Retinitis Pigmentosa.

Daniel M Lipinski1, Alun R Barnard2, Mandeep S Singh2, Chris Martin3, Edward J Lee4, Wayne I L Davies5, Robert E MacLaren6.   

Abstract

The long-term outcome of neuroprotection as a therapeutic strategy for preventing cell death in neurodegenerative disorders remains unknown, primarily due to slow disease progression and the inherent difficulty of assessing neuronal survival in vivo. Employing a murine model of retinal disease, we demonstrate that ciliary neurotrophic factor (CNTF) confers life-long protection against photoreceptor degeneration. Repetitive retinal imaging allowed the survival of intrinsically fluorescent cone photoreceptors to be quantified in vivo. Imaging of the visual cortex and assessment of visually-evoked behavioral responses demonstrated that surviving cones retain function and signal correctly to the brain. The mechanisms underlying CNTF-mediated neuroprotection were explored through transcriptome analysis, revealing widespread upregulation of proteolysis inhibitors, which may prevent cellular/extracellular matrix degradation and complement activation in neurodegenerative diseases. These findings provide insights into potential novel therapeutic avenues for diseases such as retinitis pigmentosa and amyotrophic lateral sclerosis, for which CNTF has been evaluated unsuccessfully in clinical trials.

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Year:  2015        PMID: 25896245      PMCID: PMC4539573          DOI: 10.1038/mt.2015.68

Source DB:  PubMed          Journal:  Mol Ther        ISSN: 1525-0016            Impact factor:   11.454


  61 in total

1.  Induction of suppressors of cytokine signaling (SOCS) in the retina during experimental autoimmune uveitis (EAU): potential neuroprotective role of SOCS proteins.

Authors:  H Takase; C-R Yu; X Liu; C Fujimoto; I Gery; C E Egwuagu
Journal:  J Neuroimmunol       Date:  2005-11       Impact factor: 3.478

Review 2.  Production of recombinant adeno-associated virus vectors.

Authors:  S Zolotukhin
Journal:  Hum Gene Ther       Date:  2005-05       Impact factor: 5.695

3.  Intraocular gene delivery of ciliary neurotrophic factor results in significant loss of retinal function in normal mice and in the Prph2Rd2/Rd2 model of retinal degeneration.

Authors:  F C Schlichtenbrede; A MacNeil; J W B Bainbridge; M Tschernutter; A J Thrasher; A J Smith; R R Ali
Journal:  Gene Ther       Date:  2003-03       Impact factor: 5.250

4.  Characterization of a dominant cone degeneration in a green fluorescent protein-reporter mouse with disruption of Loci associated with human dominant retinal dystrophy.

Authors:  Daniel M Lipinski; Mohammed Yusuf; Alun R Barnard; Christopher Damant; Peter Charbel Issa; Mandeep S Singh; Edward Lee; Wayne L Davies; Emanuela V Volpi; Robert E MacLaren
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-08-22       Impact factor: 4.799

5.  Repeated injections of a ciliary neurotrophic factor analogue leading to long-term photoreceptor survival in hereditary retinal degeneration.

Authors:  N H Chong; R A Alexander; L Waters; K C Barnett; A C Bird; P J Luthert
Journal:  Invest Ophthalmol Vis Sci       Date:  1999-05       Impact factor: 4.799

Review 6.  Ciliary neurotrophic factor (CNTF) for amyotrophic lateral sclerosis/motor neuron disease.

Authors:  P Bongioanni; C Reali; V Sogos
Journal:  Cochrane Database Syst Rev       Date:  2004

7.  Eliminating complement factor D reduces photoreceptor susceptibility to light-induced damage.

Authors:  Bärbel Rohrer; Yao Guo; Kannan Kunchithapautham; Gary S Gilkeson
Journal:  Invest Ophthalmol Vis Sci       Date:  2007-11       Impact factor: 4.799

8.  In vivo analysis of cone survival in mice.

Authors:  Susanne C Beck; Karin Schaeferhoff; Stylianos Michalakis; M Dominik Fischer; Gesine Huber; Norman Rieger; Olaf Riess; Bernd Wissinger; Martin Biel; Michael Bonin; Mathias W Seeliger; Naoyuki Tanimoto
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-09-08       Impact factor: 4.799

9.  Randomized trial of ciliary neurotrophic factor delivered by encapsulated cell intraocular implants for retinitis pigmentosa.

Authors:  David G Birch; Richard G Weleber; Jacque L Duncan; Glenn J Jaffe; Weng Tao
Journal:  Am J Ophthalmol       Date:  2013-05-10       Impact factor: 5.258

10.  SPLICE: a technique for generating in vitro spliced coding sequences from genomic DNA.

Authors:  Wayne L Davies; Livia S Carvalho; David M Hunt
Journal:  Biotechniques       Date:  2007-12       Impact factor: 1.993

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  30 in total

Review 1.  Let There Be Light: Gene and Cell Therapy for Blindness.

Authors:  Deniz Dalkara; Olivier Goureau; Katia Marazova; José-Alain Sahel
Journal:  Hum Gene Ther       Date:  2016-02       Impact factor: 5.695

Review 2.  Clustered Regularly Interspaced Short Palindromic Repeats: Challenges in Treating Retinal Disease.

Authors:  Micah A Chrenek; John M Nickerson; Jeffrey H Boatright
Journal:  Asia Pac J Ophthalmol (Phila)       Date:  2016 Jul-Aug

Review 3.  Gene therapy approaches for the treatment of retinal disorders.

Authors:  Lolita Petit; Claudio Punzo
Journal:  Discov Med       Date:  2016-10       Impact factor: 2.970

4.  Gene Therapy Approaches to Slow or Reverse Blindness From Inherited Retinal Degeneration: Growth Factors and Optogenetics.

Authors:  Russell N Van Gelder
Journal:  Int Ophthalmol Clin       Date:  2021-10-01

5.  Intravitreal Ciliary Neurotrophic Factor Transiently Improves Cone-Mediated Function in a CNGB3-/- Mouse Model of Achromatopsia.

Authors:  Dario Marangoni; Camasamudram Vijayasarathy; Ronald A Bush; Lisa L Wei; Rong Wen; Paul A Sieving
Journal:  Invest Ophthalmol Vis Sci       Date:  2015-10       Impact factor: 4.799

Review 6.  Principles of pharmacology in the eye.

Authors:  Sahar Awwad; Abeer H A Mohamed Ahmed; Garima Sharma; Jacob S Heng; Peng T Khaw; Steve Brocchini; Alastair Lockwood
Journal:  Br J Pharmacol       Date:  2017-10-10       Impact factor: 8.739

Review 7.  Advances in Gene Therapy for Diseases of the Eye.

Authors:  Lolita Petit; Hemant Khanna; Claudio Punzo
Journal:  Hum Gene Ther       Date:  2016-06-13       Impact factor: 5.695

8.  Precision metabolome reprogramming for imprecision therapeutics in retinitis pigmentosa.

Authors:  Salvatore Marco Caruso; Joseph Ryu; Peter Mj Quinn; Stephen H Tsang
Journal:  J Clin Invest       Date:  2020-08-03       Impact factor: 14.808

9.  Promoter Orientation within an AAV-CRISPR Vector Affects Cas9 Expression and Gene Editing Efficiency.

Authors:  Lewis E Fry; Caroline F Peddle; Marta Stevanovic; Alun R Barnard; Michelle E McClements; Robert E MacLaren
Journal:  CRISPR J       Date:  2020-08

Review 10.  Gene Therapy and Stem Cell Transplantation in Retinal Disease: The New Frontier.

Authors:  Robert E MacLaren; Jean Bennett; Steven D Schwartz
Journal:  Ophthalmology       Date:  2016-10       Impact factor: 14.277

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