Restoration of retinal regenerative potential of Müller glia by disrupting intercellular Prox1 transfer

Individuals with retinal degenerative diseases struggle to restore vision due to the inability to regenerate retinal cells. Unlike cold-blooded vertebrates, mammals lack Müller glia (MG)-mediated retinal regeneration, indicating the limited regenerative capacity of mammalian MG. Here, we identify prospero-related homeobox 1 (Prox1) as a key factor restricting this process. Prox1 accumulates in MG of degenerating human and mouse retinas but not in regenerating zebrafish. In mice, Prox1 in MG originates from neighboring retinal neurons via intercellular transfer. Blocking this transfer enables MG reprogramming into retinal progenitor cells in injured mouse retinas. Moreover, adeno-associated viral delivery of an anti-Prox1 antibody, which sequesters extracellular Prox1, promotes retinal neuron regeneration and delays vision loss in a retinitis pigmentosa model. These findings establish Prox1 as a barrier to MG-mediated regeneration and highlight anti-Prox1 therapy as a promising strategy for restoring retinal regeneration in mammals.

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Publication Details

Journal
Nature Communications
Published
2025-03-25
DOI
https://doi.org/10.1038/s41467-025-58290-8
Citations
7
Primary Topic
Retinal Development and Disorders
Type
article
Field-Weighted Citation Impact
5.64

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article

Restoration of retinal regenerative potential of Müller glia by disrupting intercellular Prox1 transfer

Hansol Jeong, Museong Kim, Jeong‐Hwan Kim, Jung-Ah Park et al.
7 citations
Nature Communications
Retinal Development and Disorders
5.64
article

Restoration of retinal regenerative potential of Müller glia by disrupting intercellular Prox1 transfer

Hansol Jeong, Museong Kim, Jeong‐Hwan Kim, Jung-Ah Park, Kihyun Park, DK Lee, Hanseul Yang, Fumio Matsuzaki, Eun Jung Lee, Jaehoon Kim, Jin Woo Kim, Seon‐Young Kim, Jeong-Soo Lee, Sooyeon Park, Ji Hyeon Shim, Hyun‐Ju Cho
article en
7 citations

Abstract

Individuals with retinal degenerative diseases struggle to restore vision due to the inability to regenerate retinal cells. Unlike cold-blooded vertebrates, mammals lack Müller glia (MG)-mediated retinal regeneration, indicating the limited regenerative capacity of mammalian MG. Here, we identify prospero-related homeobox 1 (Prox1) as a key factor restricting this process. Prox1 accumulates in MG of degenerating human and mouse retinas but not in regenerating zebrafish. In mice, Prox1 in MG originates from neighboring retinal neurons via intercellular transfer. Blocking this transfer enables MG reprogramming into retinal progenitor cells in injured mouse retinas. Moreover, adeno-associated viral delivery of an anti-Prox1 antibody, which sequesters extracellular Prox1, promotes retinal neuron regeneration and delays vision loss in a retinitis pigmentosa model. These findings establish Prox1 as a barrier to MG-mediated regeneration and highlight anti-Prox1 therapy as a promising strategy for restoring retinal regeneration in mammals.

Nature CommunicationsVol. 16(1)
Korea Advanced Institute of Science and Technology (KR), Kyoto University (JP), RIKEN Center for Biosystems Dynamics Research (JP), Nongwoo Bio (South Korea) (KR), Korea Research Institute of Bioscience and Biotechnology (KR), Korea University of Science and Technology (KR)
Korea Health Industry Development Institute, National Research Foundation of Korea, Korea Drug Development Fund
Life in Land
Openalex Percentile: Top 4%
Retinal Development and Disorders
5.64
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