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Published in: Journal of the Association for Research in Otolaryngology 4/2019

01-08-2019 | Gene Therapy in Oncology | Research Article

AAV-Mediated Neurotrophin Gene Therapy Promotes Improved Survival of Cochlear Spiral Ganglion Neurons in Neonatally Deafened Cats: Comparison of AAV2-hBDNF and AAV5-hGDNF

Authors: Patricia A. Leake, Stephen J. Rebscher, Chantale Dore‘, Omar Akil

Published in: Journal of the Association for Research in Otolaryngology | Issue 4/2019

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Abstract

Outcomes with contemporary cochlear implants (CI) depend partly upon the survival and condition of the cochlear spiral ganglion (SG) neurons. Previous studies indicate that CI stimulation can ameliorate SG neural degeneration after deafness, and brain-derived neurotrophic factor (BDNF) delivered by an osmotic pump can further improve neural survival. However, direct infusion of BDNF elicits undesirable side effects, and osmotic pumps are impractical for clinical application. In this study, we explored the potential for two adeno-associated viral vectors (AAV) to elicit targeted neurotrophic factor expression in the cochlea and promote improved SG and radial nerve fiber survival. Juvenile cats were deafened prior to hearing onset by systemic aminoglycoside injections. Auditory brainstem responses showed profound hearing loss by 16–18 days postnatal. At ~ 4 weeks of age, AAV2-GFP (green fluorescent protein), AAV5-GFP, AAV2-hBDNF, or AAV5-hGDNF (glial-derived neurotrophic factor) was injected through the round window unilaterally. For GFP immunofluorescence, animals were studied ~ 4 weeks post-injection to assess cell types transfected and their distributions. AAV2-GFP immunofluorescence demonstrated strong expression of the GFP reporter gene in residual inner (IHCs), outer hair cells (OHCs), inner pillar cells, and in some SG neurons throughout the cochlea. AAV5-GFP elicited robust transduction of IHCs and some SG neurons, but few OHCs and supporting cells. After AAV-neurotrophic factor injections, animals were studied ~ 3 months post-injection to evaluate neural survival. AAV5-hGDNF elicited a modest neurotrophic effect, with 6 % higher SG density, but had no trophic effect on radial nerve fiber survival, and undesirable ectopic fiber sprouting occurred. AAV2-hBDNF elicited a similar 6 % increase in SG survival, but also resulted in greatly improved radial nerve fiber survival, with no ectopic fiber sprouting. A further study assessed whether AAV2-hBDNF neurotrophic effects would persist over longer post-injection periods. Animals examined 6 months after virus injection showed substantial neurotrophic effects, with 14 % higher SG density and greatly improved radial nerve fiber survival. Our results suggest that AAV-neurotrophin gene therapy can elicit expression of physiological concentrations of neurotrophins in the cochlea, supporting improved SG neuronal and radial nerve fiber survival while avoiding undesirable side effects. These studies also demonstrate the potential for application of cochlear gene therapy in a large mammalian cochlea comparable to the human cochlea and in an animal model of congenital/early acquired deafness.
Literature
go back to reference Akil O, Blits B, Lustig L, Leake P (2019) Virally-mediated over-expression of GDNF elicits age- and dose-dependent neuronal toxicity and hearing loss. Hum Gene Ther 30(1):88–105CrossRefPubMedPubMedCentral Akil O, Blits B, Lustig L, Leake P (2019) Virally-mediated over-expression of GDNF elicits age- and dose-dependent neuronal toxicity and hearing loss. Hum Gene Ther 30(1):88–105CrossRefPubMedPubMedCentral
go back to reference Drennan WR, Rubinstein JT (2008) Music perception in cochlear implant users and its relationship with psychophysical capabilities. J Rehabil Res Dev 45:779–789CrossRefPubMedPubMedCentral Drennan WR, Rubinstein JT (2008) Music perception in cochlear implant users and its relationship with psychophysical capabilities. J Rehabil Res Dev 45:779–789CrossRefPubMedPubMedCentral
go back to reference Fariñas I, Jones KR, Tessarollo L et al (2001) Spatial shaping of cochlear innervation by temporally regulated neurotrophin expression. J Neurosci 21:6170–6180CrossRefPubMedPubMedCentral Fariñas I, Jones KR, Tessarollo L et al (2001) Spatial shaping of cochlear innervation by temporally regulated neurotrophin expression. J Neurosci 21:6170–6180CrossRefPubMedPubMedCentral
go back to reference Firszt JB, Holden LK, Skinner MW, Tobey EA, Petersen A, Gaggl W, Runge-Samuelson CL, Wackym PA (2004) Recognition of speech presented at soft to loud levels by adult cochlear implant recipients of three cochlear implant systems. Ear Hear 25:375–387CrossRefPubMed Firszt JB, Holden LK, Skinner MW, Tobey EA, Petersen A, Gaggl W, Runge-Samuelson CL, Wackym PA (2004) Recognition of speech presented at soft to loud levels by adult cochlear implant recipients of three cochlear implant systems. Ear Hear 25:375–387CrossRefPubMed
go back to reference Fritzsch B, Pirvola U, Ylikoski J (1999) Making and breaking the innervation of the ear: neurotrophic support during ear development and its clinical implications. Cell Tissue Res 295:369–382CrossRefPubMed Fritzsch B, Pirvola U, Ylikoski J (1999) Making and breaking the innervation of the ear: neurotrophic support during ear development and its clinical implications. Cell Tissue Res 295:369–382CrossRefPubMed
go back to reference Gao WQ, Zheng JL, Karihaloo M (1995) Neurotrophin-4/5 (NT-4/5) and brain-derived neurotrophic factor (BDNF) act at later stages of cerebellar granule cell differentiation. J Neurosci 15:2656–2667CrossRefPubMedPubMedCentral Gao WQ, Zheng JL, Karihaloo M (1995) Neurotrophin-4/5 (NT-4/5) and brain-derived neurotrophic factor (BDNF) act at later stages of cerebellar granule cell differentiation. J Neurosci 15:2656–2667CrossRefPubMedPubMedCentral
go back to reference Glueckert R, Bitsche M, Miller JM, Zhu Y, Prieskorn DM, Altschuler RA, Schrott-Fischer A (2008) Deafferentation-associated changes in afferent and efferent processes in the guinea pig cochlea and afferent regeneration with chronic intrascalar brain-derived neurotrophic factor and acidic fibroblast growth factor. J Comp Neurol 507:1602–1621. https://doi.org/10.1002/cne.21619 CrossRefPubMed Glueckert R, Bitsche M, Miller JM, Zhu Y, Prieskorn DM, Altschuler RA, Schrott-Fischer A (2008) Deafferentation-associated changes in afferent and efferent processes in the guinea pig cochlea and afferent regeneration with chronic intrascalar brain-derived neurotrophic factor and acidic fibroblast growth factor. J Comp Neurol 507:1602–1621. https://​doi.​org/​10.​1002/​cne.​21619 CrossRefPubMed
go back to reference Gyorgy B, Sage C, Indzhykulian AA, Scheffer DI, Brisson AR, Tan S, Wu X, Volak A, Mu D, Tamvakologos PI, Li Y, Fitzpatrik Z, Ericsson M, Breakefield XO, Corey DP, Maguire CA (2017) Rescue of hearing by gene delivery to inner-ear hair cells using exosomeo-associated AAV. Mol Ther 25(2):379–391. https://doi.org/10.1016/j.ymthe.2016 Gyorgy B, Sage C, Indzhykulian AA, Scheffer DI, Brisson AR, Tan S, Wu X, Volak A, Mu D, Tamvakologos PI, Li Y, Fitzpatrik Z, Ericsson M, Breakefield XO, Corey DP, Maguire CA (2017) Rescue of hearing by gene delivery to inner-ear hair cells using exosomeo-associated AAV. Mol Ther 25(2):379–391. https://​doi.​org/​10.​1016/​j.​ymthe.​2016
go back to reference Hansen MR, Zha XM, Bok J, Green SH (2001) Multiple distinct signal pathways, including an autocrine neurotrophic mechanism, contribute to the survival-promoting effect of depolarization on spiral ganglion neurons in vitro. J Neurosci 21:2256–2267CrossRefPubMedPubMedCentral Hansen MR, Zha XM, Bok J, Green SH (2001) Multiple distinct signal pathways, including an autocrine neurotrophic mechanism, contribute to the survival-promoting effect of depolarization on spiral ganglion neurons in vitro. J Neurosci 21:2256–2267CrossRefPubMedPubMedCentral
go back to reference Hegarty JL, Kay AR, Green SH (1997) Trophic support of cultured spiral ganglion neurons by depolarization exceeds and is additive with that by neurotrophins or cAMP and requires elevation of [Ca2+]i within a set range. J Neurosci 17:1959–1970CrossRefPubMedPubMedCentral Hegarty JL, Kay AR, Green SH (1997) Trophic support of cultured spiral ganglion neurons by depolarization exceeds and is additive with that by neurotrophins or cAMP and requires elevation of [Ca2+]i within a set range. J Neurosci 17:1959–1970CrossRefPubMedPubMedCentral
go back to reference Leake PA, Hradek GT, Snyder RL (1999) Chronic electrical stimulation by a cochlear implant promotes survival of spiral ganglion neurons after neonatal deafness. J Comp Neurol 412:543–562CrossRefPubMed Leake PA, Hradek GT, Snyder RL (1999) Chronic electrical stimulation by a cochlear implant promotes survival of spiral ganglion neurons after neonatal deafness. J Comp Neurol 412:543–562CrossRefPubMed
go back to reference Mackary CA, Shin J, Kujawa SG, Liberman MC, Merchant SN (2011) Age-related primary cochlear neuronal degeneration in human temporal bones. J Assoc Res Otolaryngol 12(6):711–717CrossRef Mackary CA, Shin J, Kujawa SG, Liberman MC, Merchant SN (2011) Age-related primary cochlear neuronal degeneration in human temporal bones. J Assoc Res Otolaryngol 12(6):711–717CrossRef
go back to reference Miller JM, Le Prell CG, Prieskorn DM, Wys NL, Altschuler RA (2007) Delayed neurotrophin treatment following deafness rescues spiral ganglion cells from death and promotes regrowth of auditory nerve peripheral processes: effects of brain-derived neurotrophic factor and fibroblast growth factor. J Neurosci Res 85:1959–1969. https://doi.org/10.1002/jnr.21320 CrossRefPubMed Miller JM, Le Prell CG, Prieskorn DM, Wys NL, Altschuler RA (2007) Delayed neurotrophin treatment following deafness rescues spiral ganglion cells from death and promotes regrowth of auditory nerve peripheral processes: effects of brain-derived neurotrophic factor and fibroblast growth factor. J Neurosci Res 85:1959–1969. https://​doi.​org/​10.​1002/​jnr.​21320 CrossRefPubMed
go back to reference Mouton PR (2002) Principles and practices of unbiased stereology: an introduction for bioscientists. Johns Hopkins University Press, Baltimore ISBN 0-8018-6797-5 Mouton PR (2002) Principles and practices of unbiased stereology: an introduction for bioscientists. Johns Hopkins University Press, Baltimore ISBN 0-8018-6797-5
go back to reference Ortmann M, Zwitserlood P, Knief A, Baare J, Crinkheetker S, Am Zehnhoff-Dinnesen A, Dobel C (2017) When hearing is tricky: speech processing strategies in prelingually deafened children and adolescents with cochlear implants having good and poor speech performance. PLoS One 12(1). https://doi.org/10.1371/journal.pone.0168655 Ortmann M, Zwitserlood P, Knief A, Baare J, Crinkheetker S, Am Zehnhoff-Dinnesen A, Dobel C (2017) When hearing is tricky: speech processing strategies in prelingually deafened children and adolescents with cochlear implants having good and poor speech performance. PLoS One 12(1). https://​doi.​org/​10.​1371/​journal.​pone.​0168655
go back to reference Simonelli F, Maguire AM, Testa F, Pierce EA, Mingozzi F, Bennicelli JL, Rossi S, Marshall K, Banfi S, Surace EM, Sun J, Redmond TM, Zhu X, Shindler KS, Ying GS, Ziviello C, Acerra C, Wright JF, McDonnell JW, High KA, Bennett J, Auricchio A (2010) Gene therapy for Leber’s congenital amaurosis is safe and effective through 1.5 years after vector administration. Mol Ther 18(3):643–650. https://doi.org/10.1038/mt.2009.277 CrossRefPubMed Simonelli F, Maguire AM, Testa F, Pierce EA, Mingozzi F, Bennicelli JL, Rossi S, Marshall K, Banfi S, Surace EM, Sun J, Redmond TM, Zhu X, Shindler KS, Ying GS, Ziviello C, Acerra C, Wright JF, McDonnell JW, High KA, Bennett J, Auricchio A (2010) Gene therapy for Leber’s congenital amaurosis is safe and effective through 1.5 years after vector administration. Mol Ther 18(3):643–650. https://​doi.​org/​10.​1038/​mt.​2009.​277 CrossRefPubMed
go back to reference Svirsky MA, Robbins AM, Kirk KI, Pisoni DB, Miyamoto RT (2000) Language development in profoundly deaf children with cochlear implants. Psychol Sci 11:153–158CrossRefPubMed Svirsky MA, Robbins AM, Kirk KI, Pisoni DB, Miyamoto RT (2000) Language development in profoundly deaf children with cochlear implants. Psychol Sci 11:153–158CrossRefPubMed
go back to reference Tao Y, Huang M, Shu Y, Ruprecht A, Wang H, Tang Y, Vandenberghe LH, Wang Q, Gao G, Kong WJ, Chen ZY (2018) Delivery of adeno-associated virus vectors in adult mammalian inner-ear cell subtypes without auditory dysfunction. Hum Gene Ther 29(4):492–506. https://doi.org/10.1089/hum.2017.120 Tao Y, Huang M, Shu Y, Ruprecht A, Wang H, Tang Y, Vandenberghe LH, Wang Q, Gao G, Kong WJ, Chen ZY (2018) Delivery of adeno-associated virus vectors in adult mammalian inner-ear cell subtypes without auditory dysfunction. Hum Gene Ther 29(4):492–506. https://​doi.​org/​10.​1089/​hum.​2017.​120
go back to reference Yagi M, Kanzaki S, Kawamoto K, Shin B, Shah PP, Magal E, Sheng J, Raphael Y (2000) Spiral ganglion neurons are protected from degeneration by GDNF gene therapy. J Assoc Res Otolaryngol 1:315–325PubMedPubMedCentral Yagi M, Kanzaki S, Kawamoto K, Shin B, Shah PP, Magal E, Sheng J, Raphael Y (2000) Spiral ganglion neurons are protected from degeneration by GDNF gene therapy. J Assoc Res Otolaryngol 1:315–325PubMedPubMedCentral
go back to reference Ylikoski J, Pirvola U, Virkkala J, Suvanto P, Liang XQ, Magal E, Altschuler R, Miller JM, Saarma M (1998) Guinea pig auditory neurons are protected by glial cell line-derived growth factor from degeneration after noise trauma. Hear Res 124:17–26CrossRefPubMed Ylikoski J, Pirvola U, Virkkala J, Suvanto P, Liang XQ, Magal E, Altschuler R, Miller JM, Saarma M (1998) Guinea pig auditory neurons are protected by glial cell line-derived growth factor from degeneration after noise trauma. Hear Res 124:17–26CrossRefPubMed
go back to reference Zha XM, Bishop JF, Hansen MR, Victoria L, Abbas PJ, Mouradian MM, Green SH (2001) BDNF synthesis in spiral ganglion neurons is constitutive and CREB-dependent. Hear Res 156:53–68CrossRefPubMed Zha XM, Bishop JF, Hansen MR, Victoria L, Abbas PJ, Mouradian MM, Green SH (2001) BDNF synthesis in spiral ganglion neurons is constitutive and CREB-dependent. Hear Res 156:53–68CrossRefPubMed
Metadata
Title
AAV-Mediated Neurotrophin Gene Therapy Promotes Improved Survival of Cochlear Spiral Ganglion Neurons in Neonatally Deafened Cats: Comparison of AAV2-hBDNF and AAV5-hGDNF
Authors
Patricia A. Leake
Stephen J. Rebscher
Chantale Dore‘
Omar Akil
Publication date
01-08-2019
Publisher
Springer US
Published in
Journal of the Association for Research in Otolaryngology / Issue 4/2019
Print ISSN: 1525-3961
Electronic ISSN: 1438-7573
DOI
https://doi.org/10.1007/s10162-019-00723-5

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