Failed remyelination of the non-human primate optic nerve leads to axon degeneration, retinal damages and visual dysfunction.
Sarrazin, N.; Chavret-Recculon, E.; Bachelin, C.; Felfli, M.; Arab, R.; Gilardeau, S.; Brazhnikova, E.; Dubus, E.; Yahia-Cherif, L.; Lorenceau, J.; Picaud, S.; Rosolen, S. G.; Moissonnier, P.; Pouget, P.; Baron-Van Evercooren, A.
Show abstract
White matter disorders of the CNS such as MS, lead to failure of nerve conduction and long-lasting neurological disabilities affecting a variety of sensory and motor systems including vision. While most disease-modifying therapies target the immune and inflammatory response, the promotion of remyelination has become a new therapeutic avenue, to prevent neuronal degeneration and promote recovery. Most of these strategies are developed in short-lived rodent models of demyelination, which spontaneously repair and do not reflect the size, organization, and biology of the human CNS. Thus, well-defined non-human primate models are required to efficiently advance therapeutic approaches for patients. Here, we followed the consequence of long-term toxin-induced demyelination of the macaque optic nerve on remyelination and axon preservation, as well as its impact on visual functions. Findings from oculo-motor behavior, ophthalmic examination, electrophysiology, and retinal imaging indicate visual impairment involving the optic nerve and retina. These visual dysfunctions fully correlated at the anatomical level, with sustained optic nerve demyelination, axonal degeneration, and alterations of the inner retinal layers. This non-human primate model of chronic optic nerve demyelination associated with axonal degeneration and visual dysfunction, recapitulates several key features of MS lesions and should be instrumental in providing the missing link to translate emerging repair pro-myelinating/neuroprotective therapies to the clinic for myelin disorders such as MS. Significance StatementPromotion of remyelination has become a new therapeutic avenue, to prevent neuronal degeneration and promote recovery in white matter diseases such as MS. To date most of these strategies are developed in short-lived rodent models of demyelination, which spontaneously repair. Well-defined non-human primate models closer to man would allow to efficiently advance therapeutic approaches. Here we present a non-human primate model of optic nerve demyelination that recapitulates several features of MS lesions. The model leads to failed remyelination, associated with progressive axonal degeneration and visual dysfunction, thus providing the missing link to translate emerging pre-clinical therapies to the clinic for myelin disorders such as MS.
Matching journals
The top 15 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- NFkB-signaling suppresses Müller glia-mediated neuron regeneration in the mammalian retina 94%
- Beneficial contribution of iPSC-progeny to connexin 47 dynamics during demyelination-remyelination 94%
- Ibudilast Protects Retinal Bipolar Cells from Excitotoxic Retinal Damage and Activates the mTOR Pathway 93%
Similar papers in this journal
- Cold protection allows local cryotherapy in a clinical-relevant model of traumatic optic neuropathy 95%
- MCT1-dependent energetic failure and neuroinflammation underlie optic nerve degeneration in Wolfram syndrome mice 95%
- Sex-specific attenuation of photoreceptor degeneration by reserpine in a rhodopsin P23H rat model of autosomal dominant retinitis pigmentosa 94%
Similar papers in this journal
- Transcriptomic Analysis Of The Ocular Posterior Segment Completes A Cell Atlas Of The Human Eye 93%
- RPE-specific MCT2 expression promotes cone survival in models of retinitis pigmentosa 93%
- Introduced chemokine gradients guide transplanted and regenerated retinal neurons toward their natural position in the retina 93%
Similar papers in this journal
Similar papers in this journal
- MCT2 Overexpression Rescues Metabolic Vulnerability and Protects Retinal Ganglion Cells in Two Models of Glaucoma 94%
- Altered retinal structure and function in Spinocerebellar ataxia type 3 93%
- Fibrotic scar after experimental autoimmune encephalomyelitis inhibits oligodendrocyte differentiation 92%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.