Optimization of adeno-associated viral vector-mediated transduction of the corticospinal tract: comparison of four promoters

. 2021 Feb ; 28 (1-2) : 56-74. [epub] 20200623

Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid32576975

Grantová podpora
MR/R004463/1 Medical Research Council - United Kingdom
MR/R004544/1 Medical Research Council - United Kingdom
MR/V002694/1 Medical Research Council - United Kingdom

Odkazy

PubMed 32576975
PubMed Central PMC7902269
DOI 10.1038/s41434-020-0169-1
PII: 10.1038/s41434-020-0169-1
Knihovny.cz E-zdroje

Adeno-associated viral vectors are widely used as vehicles for gene transfer to the nervous system. The promoter and viral vector serotype are two key factors that determine the expression dynamics of the transgene. A previous comparative study has demonstrated that AAV1 displays efficient transduction of layer V corticospinal neurons, but the optimal promoter for transgene expression in corticospinal neurons has not been determined yet. In this paper, we report a side-by-side comparison between four commonly used promoters: the short CMV early enhancer/chicken β actin (sCAG), human cytomegalovirus (hCMV), mouse phosphoglycerate kinase (mPGK) and human synapsin (hSYN) promoter. Reporter constructs with each of these promoters were packaged in AAV1, and were injected in the sensorimotor cortex of rats and mice in order to transduce the corticospinal tract. Transgene expression levels and the cellular transduction profile were examined after 6 weeks. The AAV1 vectors harbouring the hCMV and sCAG promoters resulted in transgene expression in neurons, astrocytes and oligodendrocytes. The mPGK and hSYN promoters directed the strongest transgene expression. The mPGK promoter did drive expression in cortical neurons and oligodendrocytes, while transduction with AAV harbouring the hSYN promoter resulted in neuron-specific expression, including perineuronal net expressing interneurons and layer V corticospinal neurons. This promoter comparison study contributes to improve transgene delivery into the brain and spinal cord. The optimized transduction of the corticospinal tract will be beneficial for spinal cord injury research.

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Hilton BJ, Bradke F. Can injured adult CNS axons regenerate by recapitulating development? Development. 2017;144:3417–29. PubMed

Mahar M, Cavalli V. Intrinsic mechanisms of neuronal axon regeneration. Nat Rev Neurosci. 2018;19:323–37. PubMed PMC

Nieuwenhuis B, Haenzi B, Andrews MR, Verhaagen J, Fawcett JW. Integrins promote axonal regeneration after injury of the nervous system. Biol Rev. 2018;93:1339–62. PubMed PMC

Hutson TH, Giovanni SD. The translational landscape in spinal cord injury: focus on neuroplasticity and regeneration. Nat Rev Neurol. 2019;16:732–45. PubMed

Gioanni Y, Lamarche M. A reappraisal of rat motor cortex organization by intracortical microstimulation. Brain Res. 1985;344:49–61. PubMed

Neafsey EJ, Bold EL, Haas G, Hurley-Gius KM, Quirk G, Sievert CF, et al. The organization of the rat motor cortex: a microstimulation mapping study. Brain Res Rev. 1986;11:77–96. PubMed

Brecht M, Krauss A, Muhammad S, Sinai-Esfahani L, Bellanca S, Margrie TW. Organization of rat vibrissa motor cortex and adjacent areas according to cytoarchitectonics, microstimulation, and intracellular stimulation of identified cells. J Comp Neurol. 2004;479:360–73. PubMed

Miller MW. The origin of corticospinal projection neurons in rat. Exp Brain Res. 1987;67:339–51. PubMed

Casale EJ, Light AR, Rustioni A. Direct projection of the corticospinal tract to the superficial laminae of the spinal cord in the rat. J Comp Neurol. 1988;278:275–86. PubMed

Liang P, Moret V, Wiesendanger M, Rouiller EM. Corticomotoneuronal connections in the rat: evidence from double-labeling of motoneurons and corticospinal axon arborizations. J Comp Neurol. 1991;311:356–66. PubMed

Brösamle C, Schwab ME. Cells of origin, course, and termination patterns of the ventral, uncrossed component of the mature rat corticospinal tract. J Comp Neurol. 1997;386:293–303. PubMed

Steward O, Zheng B, Ho C, Anderson K, Tessier-Lavigne M. The dorsolateral corticospinal tract in mice: an alternative route for corticospinal input to caudal segments following dorsal column lesions. J Comp Neurol. 2004;472:463–77. PubMed

Bareyre FM, Kerschensteiner M, Misgeld T, Sanes JR. Transgenic labeling of the corticospinal tract for monitoring axonal responses to spinal cord injury. Nat Med. 2005;11:1355–60. PubMed

Gray SJ. Gene therapy and neurodevelopmental disorders. Neuropharmacology. 2013;68:136–42. PubMed

Ojala DS, Amara DP, Schaffer DV. Adeno-associated virus vectors and neurological gene therapy. Neuroscientist. 2015;21:84–98. PubMed

Naso MF, Tomkowicz B, Perry WL, Strohl WR. Adeno-associated virus (AAV) as a vector for gene therapy. BioDrugs. 2017;31:317–34. PubMed PMC

Schultz BR, Chamberlain JS. Recombinant adeno-associated virus transduction and integration. Mol Ther. 2008;16:1189–99. PubMed PMC

Huang L-Y, Halder S, Agbandje-McKenna M. Parvovirus glycan interactions. Curr Opin Virol. 2014;7:108–18. PubMed PMC

Li C, Samulski RJ. Engineering adeno-associated virus vectors for gene therapy. Nat Rev Genet. 2020;21:255–72. PubMed

Hutson TH, Verhaagen J, Yáñez-Muñoz RJ, Moon LDF. Corticospinal tract transduction: a comparison of seven adeno-associated viral vector serotypes and a non-integrating lentiviral vector. Gene Ther. 2012;19:49–60. PubMed PMC

Watakabe A, Ohtsuka M, Kinoshita M, Takaji M, Isa K, Mizukami H, et al. Comparative analyses of adeno-associated viral vector serotypes 1, 2, 5, 8 and 9 in marmoset, mouse and macaque cerebral cortex. Neurosci Res. 2015;93:144–57. PubMed

Hadaczek P, Stanek L, Ciesielska A, Sudhakar V, Samaranch L, Pivirotto P, et al. Widespread AAV1- and AAV2-mediated transgene expression in the nonhuman primate brain: implications for Huntington’s disease. Mol Ther Methods Clin Dev. 2016;3:16037. PubMed PMC

Hammond SL, Leek AN, Richman EH, Tjalkens RB. Cellular selectivity of AAV serotypes for gene delivery in neurons and astrocytes by neonatal intracerebroventricular injection. PLoS ONE. 2017;12:e0188830. PubMed PMC

Fagoe ND, Eggers R, Verhaagen J, Mason MRJ. A compact dual promoter adeno-associated viral vector for efficient delivery of two genes to dorsal root ganglion neurons. Gene Ther. 2014;21:242–52. PubMed

Korecka J, Schouten M, Eggers R, Ulusoy A, Bossers K, Verhaagen J. Comparison of AAV serotypes for gene delivery to dopaminergic neurons in the substantia nigra. Viral Gene Ther. 2011. 10.5772/18939.

Schmitz SK, Hjorth JJJ, Joemai RMS, Wijntjes R, Eijgenraam S, de Bruijn P, et al. Automated analysis of neuronal morphology, synapse number and synaptic recruitment. J Neurosci Methods. 2011;195:185–93. PubMed

Verhaagen J, Hobo B, Ehlert EME, Eggers R, Korecka JA, Hoyng SA, et al. Small scale production of recombinant adeno-associated viral vectors for gene delivery to the nervous system. In: Boon CJF, Wijnholds J, et al., editors. Retinal gene therapy. New York, NY: Springer New York; 2018. pp. 3–17. PubMed

Cumming G, Fidler F, Vaux DL. Error bars in experimental biology. J Cell Biol. 2007;177:7–11. PubMed PMC

Koseki H, Donegá M, Lam BY, Petrova V, van Erp S, Yeo GS, et al. Selective rab11 transport and the intrinsic regenerative ability of CNS axons. eLife. 2017;6:e26956. PubMed PMC

Eva R, Koseki H, Kanamarlapudi V, Fawcett JW. EFA6 regulates selective polarised transport and axon regeneration from the axon initial segment. J Cell Sci. 2017;130:3663–75. PubMed PMC

Ueno M, Nakamura Y, Li J, Gu Z, Niehaus J, Maezawa M, et al. Corticospinal circuits from the sensory and motor cortices differentially regulate skilled movements through distinct spinal interneurons. Cell Rep. 2018;23:1286. PubMed PMC

Du K, Zheng S, Zhang Q, Li S, Gao X, Wang J, et al. Pten deletion promotes regrowth of corticospinal tract axons 1 year after spinal cord injury. J Neurosci. 2015;35:9754–63. PubMed PMC

Gennaro M, Mattiello A, Mazziotti R, Antonelli C, Gherardini L, Guzzetta A, et al. Focal stroke in the developing rat motor cortex induces age- and experience-dependent maladaptive plasticity of corticospinal system. Front Neural Circuits. 2017;11. 10.3389/fncir.2017.00047. PubMed PMC

Haenzi B, Gers-Barlag K, Akhoundzadeh H, Hutson TH, Menezes SC, Bunge MB, et al. Overexpression of the fibroblast growth factor receptor 1 (FGFR1) in a model of spinal cord injury in rats. PLoS ONE. 2016;11:e0150541. PubMed PMC

Maeda H, Fukuda S, Kameda H, Murabe N, Isoo N, Mizukami H, et al. Corticospinal axons make direct synaptic connections with spinal motoneurons innervating forearm muscles early during postnatal development in the rat. J Physiol. 2016;594:189–205. PubMed PMC

Hodgetts SI, Yoon JH, Fogliani A, Akinpelu EA, Baron-Heeris D, Houwers IGJ, et al. Cortical AAV-CNTF gene therapy combined with intraspinal mesenchymal precursor cell transplantation promotes functional and morphological outcomes after spinal cord injury in adult rats. Neural Plast. 2018. 10.1155/2018/9828725. PubMed PMC

Jin D, Liu Y, Sun F, Wang X, Liu X, He Z. Restoration of skilled locomotion by sprouting corticospinal axons induced by co-deletion of PTEN and SOCS3. Nat Commun. 2015;6:8074. PubMed PMC

Liu Y, Wang X, Li W, Zhang Q, Li Y, Zhang Z, et al. A sensitized IGF1 treatment restores corticospinal axon-dependent functions. Neuron. 2017;95:817–33. PubMed PMC

Kaludov N, Brown KE, Walters RW, Zabner J, Chiorini JA. Adeno-associated virus serotype 4 (AAV4) and AAV5 both require sialic acid binding for hemagglutination and efficient transduction but differ in sialic acid linkage specificity. J Virol. 2001;75:6884–93. PubMed PMC

Seiler MP, Miller AD, Zabner J, Halbert CL. Adeno-associated virus types 5 and 6 use distinct receptors for cell entry. Hum Gene Ther. 2006;17:10–19. PubMed

Wu Z, Miller E, Agbandje-McKenna M, Samulski RJ. α2,3 and α2,6 N-Linked sialic acids facilitate efficient binding and transduction by adeno-associated virus types 1 and 6. J Virol. 2006;80:9093–103. PubMed PMC

Mietzsch M, Broecker F, Reinhardt A, Seeberger PH, Heilbronn R. Differential adeno-associated virus serotype-specific interaction patterns with synthetic heparins and other glycans. J Virol. 2014;88:2991–3003. PubMed PMC

Kaminsky PM, Keiser NW, Yan Z, Lei-Butters DC, Engelhardt JF. Directing integrin-linked endocytosis of recombinant AAV enhances productive fak-dependent transduction. Mol Ther. 2012;20:972–83. PubMed PMC

Zhang R, Xu G, Cao L, Sun Z, He Y, Cui M, et al. Divergent engagements between adeno-associated viruses with their cellular receptor AAVR. Nat Commun. 2019;10. 10.1038/s41467-019-11668-x. PubMed PMC

Bantel-Schaal U, Hub B, Kartenbeck J. Endocytosis of adeno-associated virus type 5 leads to accumulation of virus particles in the golgi compartment. J Virol. 2002;76:2340–9. PubMed PMC

Keiser NW, Yan Z, Zhang Y, Lei-Butters DCM, Engelhardt JF. Unique characteristics of AAV1, 2, and 5 viral entry, intracellular trafficking, and nuclear import define transduction efficiency in HeLa cells. Hum Gene Ther. 2011;22:1433–44. PubMed PMC

Aschauer DF, Kreuz S, Rumpel S. Analysis of transduction efficiency, tropism and axonal transport of AAV serotypes 1, 2, 5, 6, 8 and 9 in the mouse brain. PLoS ONE. 2013;8:e76310. PubMed PMC

Salegio EA, Samaranch L, Kells AP, Mittermeyer G, Sebastian WS, Zhou S, et al. Axonal transport of adeno-associated viral vectors is serotype-dependent. Gene Ther. 2013;20:348–52. PubMed PMC

Tervo DGR, Hwang B-Y, Viswanathan S, Gaj T, Lavzin M, Ritola KD, et al. A designer AAV variant permits efficient retrograde access to projection neurons. Neuron. 2016;92:372–82. PubMed PMC

Wang Z, Maunze B, Wang Y, Tsoulfas P, Blackmore MG. Global Connectivity and function of descending spinal input revealed by 3D microscopy and retrograde transduction. J Neurosci. 2018;38:10566–81. PubMed PMC

Jayaprakash N, Nowak D, Eastwood E, Krueger N, Wang Z, Blackmore MG. Restoration of direct corticospinal communication across sites of spinal injury. bioRxiv. 2019:546374.

Kügler S, Kilic E, Bähr M. Human synapsin 1 gene promoter confers highly neuron-specific long-term transgene expression from an adenoviral vector in the adult rat brain depending on the transduced area. Gene Ther. 2003;10:337–47. PubMed

McLean JR, Smith GA, Rocha EM, Hayes MA, Beagan JA, Hallett PJ, et al. Widespread neuron-specific transgene expression in brain and spinal cord following synapsin promoter-driven AAV9 neonatal intracerebroventricular injection. Neurosci Lett. 2014;576:73–8. PubMed

Thiel G, Greengard P, Südhof TC. Characterization of tissue-specific transcription by the human synapsin I gene promoter. Proc Natl Acad Sci USA. 1991;88:3431–5. PubMed PMC

Hilton BJ, Anenberg E, Harrison TC, Boyd JD, Murphy TH, Tetzlaff W. Re-establishment of cortical motor output maps and spontaneous functional recovery via spared dorsolaterally projecting corticospinal neurons after dorsal column spinal cord injury in adult mice. J Neurosci. 2016;36:4080–92. PubMed PMC

Hioki H, Kameda H, Nakamura H, Okunomiya T, Ohira K, Nakamura K, et al. Efficient gene transduction of neurons by lentivirus with enhanced neuron-specific promoters. Gene Ther. 2007;14:872–82. PubMed

Shevtsova Z, Malik JMI, Michel U, Bähr M, Kügler S. Promoters and serotypes: targeting of adeno-associated virus vectors for gene transfer in the rat central nervous system in vitro and in vivo. Exp Physiol. 2005;90:53–9. PubMed

Andrews MR, Soleman S, Cheah M, Tumbarello DA, Mason MRJ, Moloney E, et al. Axonal localization of integrins in the CNS is neuronal type and age dependent. eNeuro. 2016;3. 10.1523/ENEURO.0029-16.2016. PubMed PMC

Delzor A, Dufour N, Petit F, Guillermier M, Houitte D, Auregan G, et al. Restricted transgene expression in the brain with cell-type specific neuronal promoters. Hum Gene Ther Methods. 2012;23:242–54. PubMed PMC

Kordower JH, Bloch J, Ma SY, Chu Y, Palfi S, Roitberg BZ, et al. Lentiviral gene transfer to the nonhuman primate brain. Exp Neurol. 1999;160:1–16. PubMed

Deglon N, Tseng JL, Bensadoun J-C, Zurn AD, Arsenijevic Y, Almeida LPD, et al. Self-inactivating lentiviral vectors with enhanced transgene expression as potential gene transfer system in Parkinson’s disease. Hum Gene Ther. 2000;11:179–90. PubMed

Alves S, Bode J, Bemelmans A-P, Kalle Cvon, Cartier N, Tews B. Ultramicroscopy as a novel tool to unravel the tropism of AAV gene therapy vectors in the brain. Sci Rep. 2016;6:1–12. PubMed PMC

Orefice NS, Souchet B, Braudeau J, Alves S, Piguet F, Collaud F, et al. Real-time monitoring of exosome enveloped-AAV spreading by endomicroscopy approach: a new tool for gene delivery in the brain. Mol Ther Methods Clin Dev. 2019;14:237–51. PubMed PMC

Nickells RW, Schmitt HM, Maes ME, Schlamp CL. AAV2-mediated transduction of the mouse retina after optic nerve injury. Invest Ophthalmol Vis Sci. 2017;58:6091–104. PubMed PMC

McCown TJ, Xiao X, Li J, Breese GR, Jude Samulski R. Differential and persistent expression patterns of CNS gene transfer by an adeno-associated virus (AAV) vector. Brain Res. 1996;713:99–107. PubMed

Klein RL, Meyer EM, Peel AL, Zolotukhin S, Meyers C, Muzyczka N, et al. Neuron-specific transduction in the rat septohippocampal or nigrostriatal pathway by recombinant adeno-associated virus vectors. Exp Neurol. 1998;150:183–94. PubMed

Paterna JC, Moccetti T, Mura A, Feldon J, Büeler H. Influence of promoter and WHV post-transcriptional regulatory element on AAV-mediated transgene expression in the rat brain. Gene Ther. 2000;7:1304–11. PubMed

Gray SJ, Foti SB, Schwartz JW, Bachaboina L, Taylor-Blake B, Coleman J, et al. Optimizing promoters for recombinant adeno-associated virus-mediated gene expression in the peripheral and central nervous system using self-complementary vectors. Hum Gene Ther. 2011;22:1143–53. PubMed PMC

Prösch S, Stein J, Staak K, Liebenthal C, Volk H-D, Krüger DH. Inactivation of the very strong HCMV immediate early promoter by DNA CpG methylation in vitro. Biol Chem. 2009;377:195–202. PubMed

Hsu C-C, Li H-P, Hung Y-H, Leu Y-W, Wu W-H, Wang F-S, et al. Targeted methylation of CMV and E1A viral promoters. Biochem Biophys Res Commun. 2010;402:228–34. PubMed

Nuo MT, Yuan JL, Yang WL, Gao XY, He N, Liang H, et al. Promoter methylation and histone modifications affect the expression of the exogenous DsRed gene in transgenic goats. Genet Mol Res. 2016;15. 10.4238/gmr.15038560. PubMed

Burger C, Gorbatyuk OS, Velardo MJ, Peden CS, Williams P, Zolotukhin S, et al. Recombinant AAV viral vectors pseudotyped with viral capsids from serotypes 1, 2, and 5 display differential efficiency and cell tropism after delivery to different regions of the central nervous system. Mol Ther. 2004;10:302–17. PubMed

Jakobsson J, Ericson C, Jansson M, Björk E, Lundberg C. Targeted transgene expression in rat brain using lentiviral vectors. J Neurosci Res. 2003;73:876–85. PubMed

Schober AL, Gagarkin DA, Chen Y, Gao G, Jacobson L, Mongin AA. Recombinant adeno-associated virus serotype 6 (rAAV6) potently and preferentially transduces rat astrocytes in vitro and in vivo. Front Cell Neurosci. 2016;10. 10.3389/fncel.2016.00262. PubMed PMC

Bucher T, Dubreil L, Colle M-A, Maquigneau M, Deniaud J, Ledevin M, et al. Intracisternal delivery of AAV9 results in oligodendrocyte and motor neuron transduction in the whole central nervous system of cats. Gene Ther. 2014;21:522–8. PubMed PMC

Pignataro D, Sucunza D, Vanrell L, Lopez-Franco E, Dopeso-Reyes IG, Vales A, et al. Adeno-Associated viral vectors serotype 8 for cell-specific delivery of therapeutic genes in the central nervous system. Front Neuroanat. 2017;11. 10.3389/fnana.2017.00002. PubMed PMC

Maes ME, Colombo G, Schulz R, Siegert S. Targeting microglia with lentivirus and AAV: recent advances and remaining challenges. Neurosci Lett. 2019;707:134310. PubMed PMC

Bartlett JS, Samulski RJ, McCown TJ. Selective and rapid uptake of adeno-associated virus type 2 in brain. Hum Gene Ther. 1998;9:1181–6. PubMed

Cucchiarini M, Ren XL, Perides G, Terwilliger EF. Selective gene expression in brain microglia mediated via adeno-associated virus type 2 and type 5 vectors. Gene Ther. 2003;10:657–67. PubMed

Rosario AM, Cruz PE, Ceballos-Diaz C, Strickland MR, Siemienski Z, Pardo M, et al. Microglia-specific targeting by novel capsid-modified AAV6 vectors. Mol Ther Methods Clin Dev. 2016;3. 10.1038/mtm.2016.26. PubMed PMC

Grace PM, Strand KA, Galer EL, Urban DJ, Wang X, Baratta MV, et al. Morphine paradoxically prolongs neuropathic pain in rats by amplifying spinal NLRP3 inflammasome activation. Proc Natl Acad Sci USA. 2016;113:E3441–50. PubMed PMC

Zhang Y, Williams PR, Jacobi A, Wang C, Goel A, Hirano AA, et al. Elevating growth factor responsiveness and axon regeneration by modulating presynaptic inputs. Neuron. 2019;103:39–51. PubMed PMC

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