Restoration of retinal regenerative potential of Müller glia by disrupting intercellular Prox1 transfer
Eun Jung Lee, Museong Kim, Sooyeon Park, Ji Hyeon Shim, Hyun‐Ju Cho, Jung-Ah Park, Kihyun Park, DK Lee, Jeong‐Hwan Kim, Jeong Hwan Kim, Fumio Matsuzaki, Seon‐Young Kim, Jaehoon Kim, Hanseul Yang, Jeong-Soo Lee, Jin Woo Kim, Jeong-Soo Lee, Jin Woo Kim, Jin Woo Kim
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.